Published on in Vol 5, No 2 (2018): Apr-Jun

Improvement of Attention-Deficit/Hyperactivity Disorder Symptoms in School-Aged Children, Adolescents, and Young Adults With Autism via a Digital Smartglasses-Based Socioemotional Coaching Aid: Short-Term, Uncontrolled Pilot Study

Improvement of Attention-Deficit/Hyperactivity Disorder Symptoms in School-Aged Children, Adolescents, and Young Adults With Autism via a Digital Smartglasses-Based Socioemotional Coaching Aid: Short-Term, Uncontrolled Pilot Study

Improvement of Attention-Deficit/Hyperactivity Disorder Symptoms in School-Aged Children, Adolescents, and Young Adults With Autism via a Digital Smartglasses-Based Socioemotional Coaching Aid: Short-Term, Uncontrolled Pilot Study

Original Paper

1Brain Power, Cambridge, MA, United States

2Massachusetts General Hospital Psychiatry Academy, Boston, MA, United States

3Department of Psychology, Harvard University, Cambridge, MA, United States

Corresponding Author:

Ned T Sahin, PhD

Brain Power

1 Broadway, 14th Floor

Cambridge, MA,

United States

Phone: 1 404 857 7179

Email: sahin@post.harvard.edu


Background: People with autism spectrum disorder (ASD) commonly experience symptoms related to attention-deficit/hyperactivity disorder (ADHD), including hyperactivity, inattention, and impulsivity. One-third of ASD cases may be complicated by the presence of ADHD. Individuals with dual diagnoses face greater barriers to accessing treatment for ADHD and respond less positively to primary pharmacologic interventions. Nonpharmacologic technology-aided tools for hyperactivity and inattention in people with ASD are being developed, although research into their efficacy and safety remains limited.

Objective: The objective of this preliminary study was to describe the changes in ADHD-related symptoms in children, adolescents, and young adults with ASD immediately after use of the Empowered Brain system, a behavioral and social communication aid for ASD running on augmented reality smartglasses.

Methods: We recruited 8 children, adolescents, and young adults with ASD (male to female ratio of 7:1, mean age 15 years, range 11.7-20.5 years) through a Web-based research signup form. The baseline score on the hyperactivity subscale of the Aberrant Behavioral Checklist (ABC-H), a measure of hyperactivity, inattention, and impulsivity, determined their classification into a high ADHD-related symptom group (n=4, ABC-H≥13) and a low ADHD-related symptom group (n=4, ABC-H<13). All participants received an intervention with Empowered Brain, where they used smartglasses-based social communication and behavioral modules while interacting with their caregiver. We then calculated caregiver-reported ABC-H scores at 24 and 48 hours after the session.

Results: All 8 participants were able to complete the intervention session. Postintervention ABC-H scores were lower for most participants at 24 hours (n=6, 75%) and for all participants at 48 hours (n=8, 100%). At 24 hours after the session, average participant ABC-H scores decreased by 54.9% in the high ADHD symptom group and by 20% in the low ADHD symptom group. At 48 hours after the session, ABC-H scores compared with baseline decreased by 56.4% in the high ADHD symptom group and by 66.3% in the low ADHD symptom group.

Conclusions: This study provides initial evidence for the possible potential of the Empowered Brain system to reduce ADHD-related symptoms, such as hyperactivity, inattention, and impulsivity, in school-aged children, adolescents, and young adults with ASD. This digital smartglasses intervention can potentially be targeted at a broader array of mental health conditions that exhibit transdiagnostic attentional and social communication deficits, including schizophrenia and bipolar disorder. Further research is required to understand the clinical importance of these observed changes and to conduct longitudinal studies on this intervention with control groups and larger sample sizes.

JMIR Ment Health 2018;5(2):e25

doi:10.2196/mental.9631

Keywords



Autism spectrum disorder (ASD) is a lifelong developmental disorder characterized by challenges in social communication and the presence of repetitive behaviors or restricted interests. Many people with ASD experience symptoms of inattention and hyperactivity, and approximately one-third of people with ASD have diagnosable attention-deficit/hyperactivity disorder (ADHD) [1,2]. There are considerable gaps in knowledge in how to provide optimal assessment and management of this group of patients [3]. Early diagnosis and intervention are beneficial for both ASD [4] and ADHD [5]. Evidence from genetic, cognitive, and behavioral research suggests that when ADHD and ASD co-occur, they may be considered a separate overarching condition [6-8], and a variety of ASD-ADHD developmental subtypes have already been proposed [9].

The combination of ASD and ADHD has been linked to greater cognitive impairment [10,11], general psychopathology [12,13], emotional processing impairment [14], and to significantly higher rates of some hyperactivity and impulsivity symptoms than in individuals with ADHD alone [15]. Furthermore, the co-occurrence of ADHD and ASD is associated with a greater risk of developing other psychiatric disorders, such as schizophrenia, bipolar disorder, and anxiety disorder, than in controls and individuals with either condition alone [16]. The pervasive nature of impairments in social communication and attention across psychiatric disorders may suggest that these deficits should be investigated transdiagnostically, an approach advocated by the US National Institute of Mental Health Research Domain Criteria framework [17]. Attentional and social communication deficits have been identified in many disorders of brain function, including schizophrenia [18,19], bipolar disorder [20,21], anxiety disorders [22], and traumatic brain injury [23,24]. Therefore, the study of individuals with combined ASD and ADHD can help elucidate the basis of a wide variety of disorders of the brain.

It is therefore important to address ADHD. While the leading approach has been psychopharmacologic medication, people with co-occurring ASD and ADHD have been found to be less likely to receive appropriate treatment for their ADHD [15] and appear to respond less favorably to treatment than do individuals with ADHD alone [25]. Additional concerns about ADHD treatment, in particular stimulant medication, focus on their long-term effectiveness [26], side effects [27], and parental reservation about their use [28]. Yet evidence also shows that leaving individuals with untreated ADHD may lead to considerable negative social and behavioral sequelae, including greater risk of academic failure [29], alcohol and drug use [30], and contact with the criminal justice system.

There has been growing interest in the use of cognitive training in ADHD, a nonpharmacologic approach that may use neurofeedback or novel digital approaches, or both. Recent studies have shown promise [31,32], although historic interventions have raised questions regarding their effectiveness [33]. There is also concern that technology may actually prove to be distracting and reduce learners’ attentiveness to educational tasks [34-36].

Little research has described the impact of digital interventions on people with ASD who demonstrate ADHD symptoms [37]. Some preliminary research has shown the utility of augmented reality interventions in ASD samples [38-40]. Intervention based on augmented reality has also been shown to help to improve ADHD symptoms in people with ASD, with improvements in both selective and sustained attention in children with ASD [38]. We have previously described the delivery of social communication coaching on augmented reality smartglasses via Empowered Brain (previously the Brain Power Autism System; Brain Power LLC) [41]. Our early pilot report on 2 boys with ASD demonstrated short-term improvements in the hyperactivity subscale of the Aberrant Behavioral Checklist (ABC-H) [41], a validated instrument that assesses hyperactivity, impulsivity, attention, and noncompliance [42]. The ABC-H has previously been used as a key outcome measure in ADHD treatment studies in children with ASD [43-47].

Objectives

In this pilot study, we explored the short-term effect of an Empowered Brain intervention on ADHD symptoms in a group of 8 children, adolescents, and young adults with ASD. We documented caregiver-reported ADHD symptoms as measured by the ABC-H. Further, we discuss the implications of these results on future research in the field.

The Empowered Brain System

Empowered Brain is a combination of modern smartglasses and educational modules targeting socioemotional and behavioral management skills [41,48]. Smartglasses are lightweight head-worn computers with a small transparent display that can provide guidance to users through both visual and audio cues (Figure 1 [49]). Empowered Brain can collect a wide variety of user data through an in-built sensor array that includes a camera, microphone, touchpad, “blink” sensor, gyroscope, and accelerometer. Empowered Brain includes modules that use these sensors to deliver social communication and cognitive skills coaching. This digital approach may be particularly valuable to both people with ASD [50] and people with ADHD [51,52].

Figure 1. Google Glass prototypical head-worn smartglasses with in-built sensors, as well as a small screen and a bone conduction speaker to provide a private audiovisual experience. Empowered Brain integrates Google Glass with a range of assistive and educational modules. User-centered design is a critical part of producing assistive technology for autistic children [49]. The modules were developed through an iterative, user-centered design and evaluation process in conjunction with behavioral specialists and families with autistic children. CPU: central processing unit; IMU: inertial measurement unit; USB: universal serial bus.
Figure 2. Demonstration of the use of the Empowered Brain system. (A) Child and partner sitting opposite one another with child wearing smartglasses. (B) Close-up view of the child wearing the smartglasses. The child can see the in-game view, displayed on the left side of the insert, through the optical display of the computerized smartglasses.

For example, Empowered Brain incorporates the Face2Face module, software that helps guide users to pay attention to socially salient visual stimuli (human faces; Figure 2 and Figure 3). The ability to pay attention to important social stimuli, and to direct gaze toward the most socially salient features of the face, has been identified as a key challenge in ASD [53]. When the Face2Face module is running, Empowered Brain is able to identify the presence of human faces within its visual field and helps direct users toward the human faces through engaging visual cartoonlike images and guidance arrows. As the user pays more visual attention to the human face, they earn points and other in-game rewards. The points stop accumulating after a short period of time to avoid coaching users to stare. Figure 2 displays the relative positioning of the user and partner when using the Face2Face module.

Using a similar approach, Empowered Brain can detect not only human faces, but also human facial emotions when running the Emotion Charades module (Figure 4). In Emotion Charades, users have a gamelike experience in which they identify the emotions of another person. Empowered Brain rewards correct answers with in-game rewards or provides guidance when needed.

Additionally, the system incorporates mechanisms to alter the difficulty associated with using each gamified app. One method is to alter the attentional challenge by displaying virtual elements that will either help to enhance attention or act as distractors to the social stimuli that the user is tasked to interact with. These virtual elements are overlaid over the user’s real-world view and include both dynamic real-time positional cues based on user movement and physiology, and reward-based virtual elements that provide feedback on the user’s in-app performance.

A series of research studies have investigated the use of Empowered Brain in ASD samples. The feasibility of using Empowered Brain in ASD was established during testing with 2 boys with ASD, both of whom demonstrated improvements in ASD symptoms as measured by the ABC [41]. Empowered Brain was safely used with no reported serious negative effects in 18 children and adults with ASD [54]. A separate report of 21 users with ASD found that Empowered Brain was well tolerated, with 91% of participants demonstrating tolerability across 3 separate measures [48]. The same study also found that 94% of participants reported the use of Empowered Brain to be comfortable. Additionally, the form factor of the computerized smartglasses of Empowered Brain has been described as desirable for school use by children with ASD [55]. Exploratory studies into the longitudinal use of Empowered Brain in school settings as a facilitative socioemotional learning tool have been reported by multiple educators as having a positive impact on student learning and social communication [56]. Empowered Brain has also been found to improve social communication as measured by longitudinal educator and parental scores on the Social Responsiveness Scale, Second Edition, a reference standard validated measure of social communication functioning in ASD [57].

The facial affective analytics component of Empowered Brain was developed in partnership with Affectiva, an emotion artificial intelligence company. The Empowered Brain also uses experimental artificial intelligence technologies developed by Amazon. This work was also made possible by Google, Inc, now known as Alphabet, Inc, who provided substantial hardware and guidance in engineering. Brain Power, the company that developed Empowered Brain, has been a long-term Glass partner in the Glass Enterprise Partnership Program at X, a company of Alphabet, Inc.

Figure 3. Empowered Brain’s Face2Face module. Face2Face is a 2-player game that encourages face-directed gaze during social interactions. (A) Child’s view on smartglasses: Face2Face detects the face in the field of view. (B) As the child maintains gaze toward the partner’s face, the progress circle fills up and the child continues to earn points (upper left). (C) When the progress circle is full, the child earns a star (lower left) and a mask is displayed as a reward. (D) Another progress circle fills up as the child demonstrates continued gaze toward the partner’s face.
Figure 4. Empowered Brain’s Emotion Charades module. (A) Emotion Charades is a 2-player game. The child, wearing smartglasses, sits across from his partner, whose app directs her to display an emotion. (B) Emotion Charades detects the partner’s face. (C) The partner displays an emotion (happy), which is detected by the system. The smartglasses show the child 2 emotions. (D) The child tilts his head to select the emotion that matches the partner’s expression, earning points for correct responses (upper right).

Institutional Review Board Approval

The methods and procedures of this study were approved by Asentral, Inc, Institutional Review Board (Newburyport, MA, USA), an affiliate of the Commonwealth of Massachusetts Department of Public Health.

Participants

We recruited participants through a Web-based research interest form. Written consent was provided by the legal guardians of children and by cognitively abled adults. Participants between 7 and 17 years old provided written assent, when they were able to.

We questioned all caregivers of participants as to whether they had a history of ADHD and whether they were currently receiving treatment for ADHD. Additionally, all participants had a baseline ABC-H and Social Communication Questionnaire (SCQ) [58].

Measures

The ABC-H is a subscale of the ABC and measures key ADHD symptoms such as inattention, impulsivity, and hyperactivity. The ABC has been extensively used in the developmentally disabled population, and the ABC-H has been used as an outcome measure of studies that have investigated the treatment of ADHD in populations with concurrent ASD [43-47]. In the assessment of ADHD symptoms in ASD, the ABC has shown itself to have superior psychometric properties, in particular validity [59] and reliability [60], compared with other rating scales of ADHD symptoms in children with developmental disorders (such as ASD). The ABC-H includes items that rate key ADHD symptoms. Specifically, the ABC-H assesses inattention and impulsivity through items that require the rater to assess whether their client is “easily distractible,” “does not pay attention to instructions,” “pays no attention when spoken to” or is “impulsive.”

Following these baseline assessments, we stratified the participants into high and low ADHD symptom groups based on their baseline ABC-H score. For the high ADHD group, we chose cutoff scores of 13 for male participants and 8 for female participants. These scores were determined by prior research that recorded the ABC scores for a sample of 666 people with developmental disorders, and found a mean ABC-H score of 13.38 for males and 8.12 for females [61].

Accordingly, we considered males with a score of 13 or higher and females with a score of 8 or higher to have high ADHD symptoms, and those with a lower score, to have low ADHD symptoms. Despite a history of ADHD diagnosis, we used the ABC-H as a stratification method, as it provided a numerical measure of recent (baseline) ADHD symptom burden. This numerical subscale allows for a more quantitative measure of change in rated items. While we obtained a clinical history of ADHD for the participants, the clinical diagnosis of ADHD in ASD is challenging [62], and it was only with the release of the Diagnostic and Statistical Manual of Mental Disorders (Fifth Edition) (DSM-5) [63] that it became possible to diagnose ADHD in an individual with ASD. Prior to the release of the DSM-5, the Diagnostic and Statistical Manual of Mental Disorders (Fourth Edition, Text Revision) specifically excluded a diagnosis of ADHD being made when an individual had a diagnosis of ASD. Therefore, while background information regarding ADHD history is important, we felt the ABC-H to be a more accurate measure of ADHD symptom load to determine the stratification into low and high ADHD symptom groups.

All participants had a baseline SCQ [58] as a validated measure of their ASD symptoms.

Procedure

All participants were accompanied by a caregiver to the testing session. We oriented the participants and their caregivers to Empowered Brain and Google Glass and measured their ability to tolerate wearing the smartglasses. Once the participants showed they were able to wear the smartglasses for at least one minute, the participants were able to use Empowered Brain social communication modules and had a series of gamified experiences while interacting with their caregiver, including using Empowered Brain modules such as Face2Face and Emotion Charades (Figure 2,Figure 3). Empowered Brain modules help users to recognize and direct their attention toward socially salient stimuli such as human faces (in particular, the central part of the face, including eye regions), emotional facial expressions, and changes in the social environment. Participants and caregivers were able to verbalize any concerns or difficulties in using Empowered Brain both during and immediately after the session. We obtained an ABC-H score at 24 hours and at 48 hours after the session through the caregiver’s report. A clinically significant change in ABC-H was determined by a 25% or more change in the score, a standard that has previously been used in combination with another scale to determine responders to ADHD treatment in an ASD population [43].

Individuals who had expressed interest via the website signup but who had a known history of epilepsy or seizure disorder were not enrolled in this study. Users who had any uncontrolled or severe medical or mental health condition that would make participation in the study predictably hazardous were also not eligible for enrollment. We obtained information regarding potential exclusions to this study directly from the caregivers of the participants.


A total of 8 children, adolescents, and young adults with ASD signed up to take part in this research (average age 15 years, range 11.7-20.5; 7 male and 1 female participants). Table 1 and Table 2 summarize participant demographics. Half of the participants had a history of ADHD (n=4, 50%), 3 of whom were receiving active treatment at the time of testing. Of note, based on their ABC-H scores, 2 participants who had a previous diagnosis of ADHD were categorized in the low ADHD symptom group, while the remaining 2 were categorized into the high ADHD symptom group. The SCQ score demonstrated that participants represented a wide range of social communication abilities, from 11 to 28 points (mean score 18).

All participants were able to use smartglasses and complete the coaching session. The high ADHD-related symptom group had a similar ASD severity to the low ADHD-related symptom group (SCQ score 18.5 vs 17.6, respectively), but consisted of younger participants (12.5 vs 17.6 years, respectively). Postintervention ABC-H scores were lower for most participants at 24 hours (n=6, 75%) and for all participants at 48 hours (n=8, 100%). At 24 hours after the session, average ABC-H scores decreased by 54.9% in the high ADHD symptom group and by 20.0% in the low ADHD symptom group. At 48 hours after the session, ABC-H scores compared with baseline decreased by 56.4% in the high ADHD symptom group (Table 3) and by 66.3% in the low ADHD symptom group (Table 4).

The high ADHD-related symptom group consisted of 4 participants who had an average ABC-H score of 25.75 at the start of the study (Table 3). The low ADHD-related symptom group consisted of 4 participants who had an average ABC-H score of 5.5 at the start of the study (Table 4). Figure 5 presents the ABC-H scores of the participants graphically.

We noted that, while the participants in the high ADHD-related symptoms group were younger, they had a similar ASD symptom severity as measured by the SCQ to the low ADHD-related symptom group. It is perhaps not a surprise to find that the high symptom group was younger, given that the ABC-H subscale is weighted toward hyperactivity, and hyperactivity is an ADHD symptom that improves with age [64].

Table 1. Individual participant demographics (n=8).
Participant identifierAge (years)SexSCQaADHDb diagnosisADHD treatment
112.6Male22NoNo
211.7Male11YesYes
312.4Male23NoNo
413.4Female18YesYes
516.9Male16YesNo
620.5Male28NoNo
719.4Male15YesYes
813.4Male12NoNo

aSCQ: Social Communication Questionnaire.

bADHD: attention-deficit/hyperactivity disorder.

Table 2. Overall participant demographics (n=8).
CharacteristicData
Age (years)

Mean (SD)15 (3.4)

Range11.7-20.5
Sex, n (%)

Male7 (87.5)

Female1 (12.5)
Prior ADHDadiagnosis, n (%)

Yes4 (50)

No4 (50)
ADHD treatment during study, n

Yes3

No5
Social Communication Questionnaire score

Mean (SD)18.1 (5.8)

Range11-28

aADHD: attention-deficit/hyperactivity disorder.

Table 3. High ADHDa-related symptom groups: ABC-Hb scores and percentage change relative to baseline (n=4).
Participant identifierBaseline score24-hour score24-hour % change48-hour score48-hour % change
1171–94.11–94.1
24840–16.742–12.5
3243–87.54–83.3
41411–21.49–35.7
Score, mean (median)25.75 (20.5)13.75 (7)N/Ac14 (6.5)N/A
Participant % change, mean (median)N/AN/A–54.9 (–52.4)N/A–56.4 (–57.5)

aADHD: attention-deficit/hyperactivity disorder.

bABC-H: hyperactivity subscale of the Aberrant Behavioral Checklist.

cN/A: not applicable.

Table 4. Low ADHDa-related symptom groups: ABC-Hb scores and percentage change relative to baseline (n=4).
Participant identifierBaseline score24-hour score24-hour % change48-hour score48-hour % change
546501–75
65504–20
7107–303–70
830–1000–100
Score, mean (median)5.5 (4.5)4.5 (5.5)N/Ac2 (2)N/A
Participant % change, mean (median)N/AN/A–20 (–15)N/A–66.3 (–72.5)

aADHD: attention-deficit/hyperactivity disorder.

bABC-H: hyperactivity subscale of the Aberrant Behavioral Checklist.

cN/A: not applicable.

Figure 5. Change in score on the hyperactivity subscale of the Aberrant Behavioral Checklist (ABC-H) by participant identifier from baseline to 48 hours after the intervention.

Principal Findings

While many people with ASD struggle with symptoms of ADHD, including hyperactivity, impulsivity, and inattention, considerable gaps in knowledge remain in regard to their optimum assessment and management [3]. The combination of ADHD and ASD has been linked not only to greater impairment [10,11] and psychopathology [12,13], but also reduced access and response to psychopharmacologic treatment for ADHD [15,25]. These are important considerations given the substantial negative sequelae of untreated ADHD [29,30]. There has been increasing interest in developing digital interventions to address the symptoms of ASD or ADHD, but few technological interventions have been studied for people with ASD and ADHD symptoms. This population may potentially benefit from such approaches.

All participants in this study managed to complete the Empowered Brain intervention session without any reported negative effects, and all participants tolerated using smartglasses for the duration of the testing session. This is important, as a major limiting factor in the use of and continued engagement with assistive technologies is their usability, tolerability, and associated negative effects.

Most participants improved their ADHD-related symptoms following the intervention at both 24 hours (n=6, 75%) and 48 hours (n=8, 100%) after the session. We noted that 1 participant in the high symptom group had a greater reduction at 24 hours than at 48 hours, and that 1 participant in the low symptom group had an increase in ADHD-related symptoms at 24 hours followed by a large decrease from baseline at 48 hours.

Mean participant ABC-H percentage changes showed a significant response in the high ADHD-related symptom group (>25% improvement in ABC-H score) at both 24 (54.9% reduction) and 48 hours (56.4% reduction). The low ADHD-related symptom group appeared to show a response at 48 hours (66.3% reduction), but not at 24 hours (20.0% reduction). While the response of the low ADHD-related symptom group appeared to be of greater magnitude, we, who include subspecialist clinicians, advise caution in assessing the low ADHD-related symptom group, given the low baseline and small absolute score changes. Such results may render the findings in this group as not being as clinically significant as the outcomes associated with the high ADHD-related symptom group. An alternative explanation may also be put forward, and that is that the technology is especially impactful for individuals with a milder ADHD symptom burden. Future larger studies would allow for more robust statistical analysis and conclusions to be made.

Limitations

There are several important limitations to this work that deserve mention. There was no control group, and the number of participants in this pilot study was relatively small (N=8), although this is a sizeable sample relative to other research on novel technologies in ASD, especially in regard to other smartglasses research [41,48]. While quantitative approaches using validated scales are very useful, future research efforts would also benefit from the use of qualitative approaches, and some early results of such methods have been reported [56].

We should certainly consider the potential for an expectancy effect [65] in using this technology, especially given that the testing session was a novel experience for both the participant and the caregiver. However, the potential for this effect should also be tempered by our knowledge that transitions or new experiences have been associated with extreme distress in people with ASD, so much so that it is a characteristic part of diagnosis [63]. We noted that none of the participants encountered any noticeable distress or problems with using the smartglasses.

It would be useful for future research to incorporate a larger sample size, with more female participants. One can also see the benefit of age-matched neurotypical and ADHD-only controls. While the ABC-H is a very useful scale to use in this context, the use of broader ADHD-related measures would also provide for further insights. Despite our findings, the broader generalizability of our results to the wider ASD population will remain limited until further research is undertaken.

Future Research

We hope that this study can pave the way for more funding and interest to study the potential application of this emerging technology to not just dually diagnosed ADHD and ASD samples, but more broadly to other categorical psychiatric diagnoses that are also associated with both attentional and social communication impairments. Such diagnoses include schizophrenia, bipolar disorder, and anxiety disorder. While deficits in social communication occur across many psychiatric disorders, most digital social communication interventions have been studied in ASD alone [66]. Therefore, research and development of an intervention that can target transdiagnostic symptoms could be valuable in both clinical scenarios and in research using the Research Domain Criteria framework.

Smartglasses may have a particularly unique role in this respect, as they also contain a variety of quantitative sensors that are located more closely than any other wearable technology to the main perceptual apparatus of the brain. These sensors can collect and help analyze sensor data to help classify human behavior. This digital phenotyping approach aims to detect changes in affective and behavioral states associated with both improvements and deteriorations in psychiatric disorders, and to help to identify new methods to subtype disorders [67].

Empowered Brain is being developed as a tool that can be used by caregivers, therapists, and educators to deliver socioemotional interventions to users with ASD. It is designed as a tool that can be used on a daily basis for 10 to 20 minutes per intervention. While this study reports on the impact of Empowered Brain on ADHD symptoms after a single intervention, further research is required to understand how the longitudinal use of this technology may affect ADHD symptoms in people with ASD. This technology also has the potential to address the attentional and social communication deficits that are transdiagnostically present across psychiatric disorders. Data collection via sensors that are proximally situated to the principal human perceptual organs may result in a more ecologically valid digital phenotyping approach. This digital phenotyping approach may aid the research of proposed developmental subtypes of a distinct ASD-ADHD combination disorder and, more broadly, psychiatric and brain injury-related disorders.

Conclusion

Empowered Brain is a smartglasses-based social communication intervention that has been previously shown to improve social communication functioning in ASD. This study provides early evidence for the possible potential of Empowered Brain to reduce ADHD symptoms, such as hyperactivity, inattention, and impulsivity, in school-aged children, adolescents, and young adults with ASD. Our results also suggest that, despite concerns about increased distraction and reduced attentiveness, the Empowered Brain did not result in any increased ADHD symptoms in any of the participants at 48 hours after the intervention.

Acknowledgments

The authors thank Google, Inc, for a generous grant and the Glass team at X (formerly Google X) for technical guidance on Glass software development. This work was supported by the Office of the Assistant Secretary of Defense for Health Affairs through the Autism Research Program under Award No. W81XWH 17-1-0449. Early work to transform smartglasses into biomedical sensors was supported in part by the United States Army Medical Research and Materiel Command under Contract No. W81XWH-14-C-0007 (awarded to TIAX, LLC). Opinions, interpretations, conclusions, and recommendations are those of the authors and are not necessarily endorsed by the US Department of Defense.

Conflicts of Interest

NTS is the inventor of the Empowered Brain system. All of the authors have affiliations at Brain Power, a neurotechnology company that supported this report. Brain Power receives funding support from US Federal and Congressional sources.

  1. Leyfer OT, Folstein SE, Bacalman S, Davis NO, Dinh E, Morgan J, et al. Comorbid psychiatric disorders in children with autism: interview development and rates of disorders. J Autism Dev Disord. Oct 2006;36(7):849-861. [CrossRef] [Medline]
  2. Rosenberg RE, Kaufmann WE, Law JK, Law PA. Parent report of community psychiatric comorbid diagnoses in autism spectrum disorders. Autism Res Treat. 2011;2011:405849. [FREE Full text] [CrossRef] [Medline]
  3. May T, Brignell A, Hawi Z, Brereton A, Tonge B, Bellgrove MA, et al. Trends in the overlap of autism spectrum disorder and attention deficit hyperactivity disorder: prevalence, clinical management, language and genetics. Curr Dev Disord Rep. Jan 17, 2018;5(1):49-57. [CrossRef]
  4. Estes A, Munson J, Rogers SJ, Greenson J, Winter J, Dawson G. Long-term outcomes of early intervention in 6-year-old children with autism spectrum disorder. J Am Acad Child Adolesc Psychiatry. Jul 2015;54(7):580-587. [FREE Full text] [CrossRef] [Medline]
  5. DuPaul GJ, Kern L, Caskie GIL, Volpe RJ. Early intervention for young children with attention deficit hyperactivity disorder: prediction of academic and behavioral outcomes. School Psychol Rev. Mar 2015;44(1):3-20. [CrossRef]
  6. Ronald A, Simonoff E, Kuntsi J, Asherson P, Plomin R. Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample. J Child Psychol Psychiatry. May 2008;49(5):535-542. [CrossRef] [Medline]
  7. van der Meer JMJ, Oerlemans AM, van Steijn DJ, Lappenschaar MGA, de Sonneville LMJ, Buitelaar JK, et al. Are autism spectrum disorder and attention-deficit/hyperactivity disorder different manifestations of one overarching disorder? Cognitive and symptom evidence from a clinical and population-based sample. J Am Acad Child Adolesc Psychiatry. Nov 2012;51(11):1160-1172.e3. [CrossRef] [Medline]
  8. Ames CS, White SJ. Are ADHD traits dissociable from the autistic profile? Links between cognition and behaviour. J Autism Dev Disord. Mar 2011;41(3):357-363. [CrossRef] [Medline]
  9. Rommelse N, Buitelaar JK, Hartman CA. Structural brain imaging correlates of ASD and ADHD across the lifespan: a hypothesis-generating review on developmental ASD-ADHD subtypes. J Neural Transm (Vienna). Feb 2017;124(2):259-271. [FREE Full text] [CrossRef] [Medline]
  10. Sinzig J, Walter D, Doepfner M. Attention deficit/hyperactivity disorder in children and adolescents with autism spectrum disorder: symptom or syndrome? J Atten Disord. Sep 2009;13(2):117-126. [CrossRef] [Medline]
  11. Yerys BE, Wallace GL, Sokoloff JL, Shook DA, James JD, Kenworthy L. Attention deficit/hyperactivity disorder symptoms moderate cognition and behavior in children with autism spectrum disorders. Autism Res. Dec 2009;2(6):322-333. [FREE Full text] [CrossRef] [Medline]
  12. Holtmann M, Bolte S, Poustka F. Attention deficit hyperactivity disorder symptoms in pervasive developmental disorders: association with autistic behavior domains and coexisting psychopathology. Psychopathology. 2007;40(3):172-177. [CrossRef] [Medline]
  13. Jang J, Matson JL, Williams LW, Tureck K, Goldin RL, Cervantes PE. Rates of comorbid symptoms in children with ASD, ADHD, and comorbid ASD and ADHD. Res Dev Disabil. Aug 2013;34(8):2369-2378. [CrossRef] [Medline]
  14. Tye C, Battaglia M, Bertoletti E, Ashwood KL, Azadi B, Asherson P, et al. Altered neurophysiological responses to emotional faces discriminate children with ASD, ADHD and ASD+ADHD. Biol Psychol. Dec 2014;103:125-134. [CrossRef] [Medline]
  15. Joshi G, Faraone SV, Wozniak J, Tarko L, Fried R, Galdo M, et al. Symptom profile of ADHD in youth with high-functioning autism spectrum disorder: a comparative study in psychiatrically referred populations. J Atten Disord. Aug 2017;21(10):846-855. [FREE Full text] [CrossRef] [Medline]
  16. Chen M, Wei H, Chen L, Su T, Bai Y, Hsu J, et al. Autistic spectrum disorder, attention deficit hyperactivity disorder, and psychiatric comorbidities: a nationwide study. Res Autism Spectr Disord. Feb 2015;10:1-6. [CrossRef]
  17. Insel T, Cuthbert B, Garvey M, Heinssen R, Pine DS, Quinn K, et al. Research domain criteria (RDoC): toward a new classification framework for research on mental disorders. Am J Psychiatry. Jul 2010;167(7):748-751. [CrossRef] [Medline]
  18. Morrison KE, Pinkham AE, Penn DL, Kelsven S, Ludwig K, Sasson NJ. Distinct profiles of social skill in adults with autism spectrum disorder and schizophrenia. Autism Res. May 2017;10(5):878-887. [CrossRef] [Medline]
  19. Gold JM, Robinson B, Leonard CJ, Hahn B, Chen S, McMahon RP, et al. Selective attention, working memory, and executive function as potential independent sources of cognitive dysfunction in schizophrenia. Schizophr Bull. Nov 11, 2017. [CrossRef] [Medline]
  20. Pagliaccio D, Wiggins JL, Adleman NE, Harkins E, Curhan A, Towbin KE, et al. Behavioral and neural sustained attention deficits in bipolar disorder and familial risk of bipolar disorder. Biol Psychiatry. Nov 01, 2017;82(9):669-678. [CrossRef] [Medline]
  21. McClure EB, Treland JE, Snow J, Schmajuk M, Dickstein DP, Towbin KE, et al. Deficits in social cognition and response flexibility in pediatric bipolar disorder. Am J Psychiatry. Sep 2005;162(9):1644-1651. [CrossRef] [Medline]
  22. Halls G, Cooper PJ, Creswell C. Social communication deficits: specific associations with social anxiety disorder. J Affect Disord. Feb 01, 2015;172:38-42. [FREE Full text] [CrossRef] [Medline]
  23. Beaulieu-Bonneau S, Fortier-Brochu E, Ivers H, Morin CM. Attention following traumatic brain injury: neuropsychological and driving simulator data, and association with sleep, sleepiness, and fatigue. Neuropsychol Rehabil. Mar 2017;27(2):216-238. [CrossRef] [Medline]
  24. Steel J, Ferguson A, Spencer E, Togher L. Social communication assessment during post-traumatic amnesia and the post-acute period after traumatic brain injury. Brain Inj. 2017;31(10):1320-1330. [CrossRef] [Medline]
  25. Research Units on Pediatric Psychopharmacology Autism Network. Randomized, controlled, crossover trial of methylphenidate in pervasive developmental disorders with hyperactivity. Arch Gen Psychiatry. Nov 2005;62(11):1266-1274. [CrossRef] [Medline]
  26. van de Loo-Neus GHH, Rommelse N, Buitelaar JK. To stop or not to stop? How long should medication treatment of attention-deficit hyperactivity disorder be extended? Eur Neuropsychopharmacol. Aug 2011;21(8):584-599. [CrossRef] [Medline]
  27. Graham J, Banaschewski T, Buitelaar J, Coghill D, Danckaerts M, Dittmann RW, et al. European Guidelines Group. European guidelines on managing adverse effects of medication for ADHD. Eur Child Adolesc Psychiatry. Jan 2011;20(1):17-37. [FREE Full text] [CrossRef] [Medline]
  28. Berger I, Dor T, Nevo Y, Goldzweig G. Attitudes toward attention-deficit hyperactivity disorder (ADHD) treatment: parents' and children's perspectives. J Child Neurol. Sep 2008;23(9):1036-1042. [CrossRef] [Medline]
  29. Daley D, Birchwood J. ADHD and academic performance: why does ADHD impact on academic performance and what can be done to support ADHD children in the classroom? Child Care Health Dev. Jul 2010;36(4):455-464. [CrossRef] [Medline]
  30. Hammerness P, Petty C, Faraone SV, Biederman J. Do stimulants reduce the risk for alcohol and substance use in youth with ADHD? A secondary analysis of a prospective, 24-month open-label study of osmotic-release methylphenidate. J Atten Disord. Jan 2017;21(1):71-77. [CrossRef] [Medline]
  31. Mishra J, Sagar R, Joseph AA, Gazzaley A, Merzenich MM. Training sensory signal-to-noise resolution in children with ADHD in a global mental health setting. Transl Psychiatry. Apr 12, 2016;6:e781. [FREE Full text] [CrossRef] [Medline]
  32. Blandón D, Muñoz J, Lopez D, Gallo O. Influence of a BCI neurofeedback videogame in children with ADHD. Quantifying the brain activity through an EEG signal processing dedicated toolbox. 2016. Presented at: 2016 IEEE 11th Colombian Computing Conference (CCC); Sep 27-30, 2016; Popayán, Colombia.
  33. Cortese S, Ferrin M, Brandeis D, Holtmann M, Aggensteiner P, Daley D, et al. European ADHD Guidelines Group (EAGG). Neurofeedback for attention-deficit/hyperactivity disorder: meta-analysis of clinical and neuropsychological outcomes from randomized controlled trials. J Am Acad Child Adolesc Psychiatry. Jun 2016;55(6):444-455. [CrossRef] [Medline]
  34. McCoy B. Digital distractions in the classroom phase II: student classroom use of digital devices for non-class related purposes. J Media Educ. 2016;7(1):5-32.
  35. Lowe T. Utilizing Cell Phones as a Learning Tool in the Classroom: Preventing Distractions While Increasing Student Engagement [dissertation]. San Marcos, CA. California State University San Marcos; 2017.
  36. Thomas K, Muñoz MA. Hold the phone! High school students' perceptions of mobile phone integration in the classroom. Am Second Educ. 2016;44(3):19.
  37. Sonuga-Barke EJS, Brandeis D, Cortese S, Daley D, Ferrin M, Holtmann M, et al. Nonpharmacological interventions for ADHD: systematic review and meta-analyses of randomized controlled trials of dietary and psychological treatments. Am J Psychiatry. Mar 2013;170(3):275-289. [CrossRef] [Medline]
  38. Escobedo L, Tentori M, Quintana E, Favela J, Garcia-Rosas D. Using augmented reality to help children with autism stay focused. IEEE Pervasive Comput. Jan 2014;13(1):38-46. [CrossRef]
  39. da Silva CA, Fernandes AR, Grohmann AP. STAR: Speech Therapy with Augmented Reality for children with autism spectrum disorders. In: Cordeiro J, Hammoudi S, Maciaszek L, Camp O, Filipe J, editors. Enterprise Information Systems. ICEIS 2014. Lecture Notes in Business Information Processing, volume 227. Cham, Switzerland. Springer International Publishing AG; 2015:379-396.
  40. Escobedo L, Nguyen D, Boyd L, Hirano S, Rangel A, Garcia-Rosas D. MOSOCO: a mobile assistive tool to support children with autism practicing social skills in real-life situations. 2012. Presented at: SIGCHI Conference on Human Factors in Computing Systems; May 5-10, 2012; Austin TX, USA.
  41. Liu R, Salisbury JP, Vahabzadeh A, Sahin NT. Feasibility of an autism-focused augmented reality smartglasses system for social communication and behavioral coaching. Front Pediatr. 2017;5:145. [FREE Full text] [CrossRef] [Medline]
  42. Aman MG, Singh NN, Stewart AW, Field CJ. The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects. Am J Ment Defic. Mar 1985;89(5):485-491. [Medline]
  43. Arnold LE, Aman MG, Cook AM, Witwer AN, Hall KL, Thompson S, et al. Atomoxetine for hyperactivity in autism spectrum disorders: placebo-controlled crossover pilot trial. J Am Acad Child Adolesc Psychiatry. Oct 2006;45(10):1196-1205. [CrossRef] [Medline]
  44. Bent S, Hendren RL, Zandi T, Law K, Choi J, Widjaja F, et al. Internet-based, randomized, controlled trial of omega-3 fatty acids for hyperactivity in autism. J Am Acad Child Adolesc Psychiatry. Jun 2014;53(6):658-666. [FREE Full text] [CrossRef] [Medline]
  45. Troost PW, Steenhuis M, Tuynman-Qua HG, Kalverdijk LJ, Buitelaar JK, Minderaa RB, et al. Atomoxetine for attention-deficit/hyperactivity disorder symptoms in children with pervasive developmental disorders: a pilot study. J Child Adolesc Psychopharmacol. Oct 2006;16(5):611-619. [CrossRef] [Medline]
  46. Posey DJ, Wiegand RE, Wilkerson J, Maynard M, Stigler KA, McDougle CJ. Open-label atomoxetine for attention-deficit/ hyperactivity disorder symptoms associated with high-functioning pervasive developmental disorders. J Child Adolesc Psychopharmacol. Oct 2006;16(5):599-610. [CrossRef] [Medline]
  47. Charnsil C. Efficacy of atomoxetine in children with severe autistic disorders and symptoms of ADHD: an open-label study. J Atten Disord. Nov 2011;15(8):684-689. [CrossRef] [Medline]
  48. Keshav NU, Salisbury JP, Vahabzadeh A, Sahin NT. Social communication coaching smartglasses: well tolerated in a diverse sample of children and adults with autism. JMIR Mhealth Uhealth. Sep 21, 2017;5(9):e140. [FREE Full text] [CrossRef] [Medline]
  49. Lubas M, Mitchell J, De Leo G. User-centered design and augmentative and alternative communication apps for children with autism spectrum disorders. SAGE Open. May 30, 2014;4(2):215824401453750. [CrossRef]
  50. Whyte EM, Smyth JM, Scherf KS. Designing serious game interventions for individuals with autism. J Autism Dev Disord. Dec 2015;45(12):3820-3831. [CrossRef] [Medline]
  51. Dovis S, Van der Oord S, Wiers RW, Prins PJM. Can motivation normalize working memory and task persistence in children with attention-deficit/hyperactivity disorder? The effects of money and computer-gaming. J Abnorm Child Psychol. Jul 2012;40(5):669-681. [FREE Full text] [CrossRef] [Medline]
  52. Prins PJM, Dovis S, Ponsioen A, ten Brink E, van der Oord S. Does computerized working memory training with game elements enhance motivation and training efficacy in children with ADHD? Cyberpsychol Behav Soc Netw. Mar 2011;14(3):115-122. [CrossRef] [Medline]
  53. Klin A, Jones W, Schultz R, Volkmar F, Cohen D. Visual fixation patterns during viewing of naturalistic social situations as predictors of social competence in individuals with autism. Arch Gen Psychiatry. Sep 2002;59(9):809-816. [Medline]
  54. Sahin N, Keshav N, Salisbury J, Vahabzadeh A. bioRxiv. 2017. URL: https://www.biorxiv.org/content/early/2017/08/06/164335 [accessed 2018-03-20] [WebCite Cache]
  55. Sahin NT, Keshav NU, Salisbury JP, Vahabzadeh A. Second version of Google Glass as a wearable socio-affective aid in children with autism: theoretical basis, usability, and desirability in schools. JMIR Hum Factors. Jan 04, 2018;5(1):e1. [FREE Full text] [CrossRef] [Medline]
  56. Keshav N, Vahabzadeh A, Abdus-Sabur R, Liu R, Huey K, Salisbury J. PsyArXiv. 2018. URL: https://psyarxiv.com/xpduy/ [accessed 2018-03-20] [WebCite Cache]
  57. Sahin N, Abdus-Sabur R, Keshav N, Liu R, Salisbury J, Vahabzadeh A. PsyArXiv. 2018. URL: https://psyarxiv.com/h2eu8/ [accessed 2018-03-20] [WebCite Cache]
  58. Rutter M, Bailey A, Lord C. The Social Communication Questionnaire: Manual. Torrance, CA. Western Psychological Services; 2003.
  59. Miller ML, Fee VE, Jones CJ. Psychometric properties of ADHD rating scales among children with mental retardation. Res Dev Disabil. 2004;25(5):477-492. [CrossRef] [Medline]
  60. Miller ML, Fee VE, Netterville AK. Psychometric properties of ADHD rating scales among children with mental retardation I: reliability. Res Dev Disabil. 2004;25(5):459-476. [CrossRef] [Medline]
  61. Marshburn EC, Aman MG. Factor validity and norms for the aberrant behavior checklist in a community sample of children with mental retardation. J Autism Dev Disord. Sep 1992;22(3):357-373. [Medline]
  62. Stevens T, Peng L, Barnard-Brak L. The comorbidity of ADHD in children diagnosed with autism spectrum disorder. Res Autism Spectr Disord. Nov 2016;31:11-18. [CrossRef]
  63. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders Fifth Edition (DSM-5). Washington, DC. American Psychiatric Association; 2013.
  64. Kooij SJJ, Bejerot S, Blackwell A, Caci H, Casas-Brugué M, Carpentier PJ, et al. European consensus statement on diagnosis and treatment of adult ADHD: the European Network Adult ADHD. BMC Psychiatry. Sep 03, 2010;10:67. [FREE Full text] [CrossRef] [Medline]
  65. Kirsch I. Response expectancy as a determinant of experience and behavior. Am Psychol. Feb 1985;40(11):1189.
  66. Wieckowski AT, White SW. Application of technology to social communication impairment in childhood and adolescence. Neurosci Biobehav Rev. Mar 2017;74(Pt A):98-114. [CrossRef] [Medline]
  67. Onnela J, Rauch SL. Harnessing smartphone-based digital phenotyping to enhance behavioral and mental health. Neuropsychopharmacology. Jun 2016;41(7):1691-1696. [CrossRef] [Medline]


ABC-H: hyperactivity subscale of the Aberrant Behavioral Checklist
ADHD: attention-deficit/hyperactivity disorder
ASD: autism spectrum disorder
DSM-5: Diagnostic and Statistical Manual of Mental Disorders (Fifth Edition)
SCQ: Social Communication Questionnaire


Edited by G Eysenbach; submitted 11.12.17; peer-reviewed by S Aggarwal, K Bul, A Benis; comments to author 23.01.18; revised version received 20.02.18; accepted 09.03.18; published 02.04.18.

Copyright

©Arshya Vahabzadeh, Neha U Keshav, Joseph P Salisbury, Ned T Sahin. Originally published in JMIR Mental Health (http://mental.jmir.org), 02.04.2018.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Mental Health, is properly cited. The complete bibliographic information, a link to the original publication on http://mental.jmir.org/, as well as this copyright and license information must be included.