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A Mightier Healthcare System

A Mightier Healthcare System: Introducing a Game-based Pediatric Mental Health Intervention Into Payor-sponsored Care to Evaluate Financial and Clinical Outcomes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04732806
Enrollment
183
Registered
2021-02-01
Start date
2021-03-10
Completion date
2025-10-01
Last updated
2025-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emotional Dysregulation

Brief summary

Access to effective pediatric mental health treatment is a major public health concern in the United States as paucity of pediatric providers leading to long wait times, financial burden, and stigma pose significant barriers to treatment. Digital mental health promises to remedy many chronic problems faced in providing timely and accessible mental health interventions to children. With that in mind, the investigators and Neuromotion Inc. created Mightier, an app-based heart rate biofeedback videogame platform designed to teach and facilitate practice of emotional regulation skills. The technology behind Mightier is backed by three trials showing clinical efficacy and since commercial launch 75% of families who have engaged with the product report improvement. However, Neuromotion's core mission remains increasing access to care, and the direct-to-consumer distribution of digital health also faces access challenges. The investigators propose that access to effective digital mental health interventions can be increased by meeting families where they already know to seek care: the traditional healthcare system. The investigators have partnered with a nationwide behavioral health insurance provider to pilot the integration of Mightier with traditional healthcare. Families will be recruited via direct outreach, social media, or healthcare provider referral. Participating children will be randomized into Mightier or treatment as usual control groups for 6 months. Behavioral healthcare utilization will be observed for 12 months. Through this work the investigators will demonstrate the value of Mightier to various stakeholders via decreased long-term healthcare utilization, confirm that Mightier use results in decreased symptoms of emotional dysregulation, irritability, and parent stress, and explore relationships among Mightier use, healthcare utilization, and symptoms. Ultimately this work will pave the way forward for large scale integration of digital healthcare and more traditional healthcare avenues while simultaneously increasing Mightier's ability to reach children in need.

Interventions

BEHAVIORALMightier video games

Biofeedback video game play in home

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Magellan Healthcare
CollaboratorUNKNOWN
Neuromotion Labs
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
8 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

Inclusion: * Age 8-12 * Insurance provided by Magellan Healthcare OR participant is covered by insurance in Massachusetts and has access to Explanation of Benefits information via online portal * Has made a behavioral health claim in the past year * MOAS score of greater than or equal to 2 * Evidence of ADHD, ODD, CD, DMDD, IED, or ASD by MINI-KID * Parent or guardian is fluent in English * WiFi at home (for Mightier tablet connection) * Access to a computer or tablet in the home Exclusion: * IQ \< 70 (by medical record or clinician judgment) * Extremely limited verbal capacity * Change in medication or medication dosage in the past month or planned change in medication or medication dosage in the next month * Active suicidal ideation * History of suicide attempt and current depression * Physical limitations that preclude the use of Mightier * Sensory sensitivities that would preclude wearing an arm (or leg) heart rate monitor * Evidence of psychosis, mania, alcohol use disorder, substance use disorder, or PTSD by MINI-Kid * Ongoing or within the month prior to baseline visit placement in foster care or residential facility

Design outcomes

Primary

MeasureTime frameDescription
Behavioral healthcare utilization cost12 MonthsDollars spent on behavioral healthcare over the study period.
Change in Modified Overt Aggression Scale (MOAS) from baseline to 3 MonthsBaseline, 3 monthsThe MOAS is a 5-point parent rated scale that rates the severity of four types of aggression: verbal, against property, against self (auto-aggression), and physical towards others. Scores range from 0-100 with lower scores representing less aggression (better outcome).

Secondary

MeasureTime frameDescription
Clinical Global Impression - Improvement, Irritability/Anger (CGI-I Irritability/Anger)3 monthsThe CGI-I scale requires the clinician to rate total improvement whether or not, in the raters judgment, it is due to treatment. The clinician compares the patient's condition at baseline to the time of rating on a scale ranging from 1 (very much improved) to 7 (very much worse)
Clinical Global Impression - Improvement, Aggression (CGI-I Aggression)3 monthsThe CGI-I scale requires the clinician to rate total improvement whether or not, in the raters judgment, it is due to treatment. The clinician compares the patient's condition at baseline to the time of rating on a scale ranging from 1 (very much improved) to 7 (very much worse)
Clinical Global Impression - Improvement, Oppositional/Defiant Behavior (CGI-I Oppositional/Defiant Behavior)3 monthsThe CGI-I scale requires the clinician to rate total improvement whether or not, in the raters judgment, it is due to treatment. The clinician compares the patient's condition at baseline to the time of rating on a scale ranging from 1 (very much improved) to 7 (very much worse)
Clinical Global Impression - Improvement, Disruptive Behavior (CGI-I Disruptive Behavior)3 monthsThe CGI-I scale requires the clinician to rate total improvement whether or not, in the raters judgment, it is due to treatment. The clinician compares the patient's condition at baseline to the time of rating on a scale ranging from 1 (very much improved) to 7 (very much worse)
Change in Parent Confidence and Resources from baseline to 3 MonthsBaseline, 3 monthsTwo 5 item questions regarding parent confidence in their ability to manage their child's behaviors and adequacy of resources to manage their child's behaviors
Change in NIH-Emotion Toolbox from baseline to 3 MonthsBaseline, 3 monthsThe NIH toolbox for emotion was developed to create a standardized, comprehensive, and concise battery of tests that can recognize the full spectrum of emotional experiences and their impacts on health and wellbeing. The NIH Toolbox for emotion includes 4 subdomains: negative affect, psychological well-being, stress and self-efficacy, and social relationships. For the age range of 8-12, self-report and proxy measures are available. Given that we expect a wide range of cognitive, developmental, and metacognitive abilities, proxy report measures will be used.
Change in Disruptive Behavior Disorder Rating Scale (DBDRS) - Oppositional/Defiant Factor Score from baseline to 3 MonthsBaseline, 3 monthsThe DBDRS is a 45-item scale that evaluates symptoms of Oppositional Defiant Disorder (ODD), Conduct Disorder (CD), and Attention Deficit Hyperactivity Disorder (ADHD) from the parent's perspective. Scores range from 0-135 with lower scores representing fewer behaviors associated with the above disorders (better outcome). This secondary outcome will include the Oppositional/Defiant Factor Score consisting of items 3, 13, 15, 17, 24, 26, 28, and 39.
Change in Affective Reactivity Index - Parent (ARI-P) from baseline to 3 MonthsBaseline, 3 monthsThe ARI is a 7-item scale that consists of 6 symptom items and 1 impairment item. The scale was designed to determine irritable mood rather than behavioral consequences such as hostility and acts of aggression. Scores range from 0 - 12 with lower scores representing less irritability.
Change in Parent Stress Index - Short Form (PSI-SF) from baseline to 3 MonthsBaseline, 3 monthsThe PSI-SF is a 36 item parent report scale that evaluates the extent and source of parent stress in the form of three subscales: Parental Distress, Parent-Child Dysfunctional Interaction, and Difficult Child. Total scores range from 36-180 with lower scores representing less parent stress.

Other

MeasureTime frameDescription
Change in Disruptive Behavior Disorder Rating Scale (DBDRS) - Total ScoreBaseline, 3 MonthsThe DBDRS is a 45-item scale that evaluates symptoms of Oppositional Defiant Disorder (ODD), Conduct Disorder (CD), and Attention Deficit Hyperactivity Disorder (ADHD) from the parent's perspective. Scores range from 0-135 with lower scores representing fewer behaviors associated with the above disorders (better outcome).
Behavioral healthcare utilization cost -- billed as medical12 MonthsDollars spent on healthcare billed as medical cost, but related to behavioral or mental health indications, over the study period
Customer Satisfaction3 monthsEvaluated in the Mightier group only. Customer satisfaction will be rated using a single, parent/guardian response item. Response options will be extremely dissatisfied, somewhat dissatisfied, neither satisfied not dissatisfied, somewhat satisfied, or extremely satisfied.
Net Promoter Score3 monthsEvaluated in the Mightier group only. Net Promotor Score represents the industry standard for evaluating customer willingness to recommend a product. The rating consists of a single parent/guardian report item with responses options ranging from 0 (not at all likely) to 10 (extremely likely). When scores are aggregated, Net Promoter Score is expressed as the percentage of customers who rated their likelihood to recommend the product as 9 or 10 minus the percentage of customers rating this at 6 or below.
Heart Rate1hz intervals when playing game for 6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026