- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01917838
Mobile Health Solutions for Behavioral Skill Implementation Through Homework (MHealth)
The goal of this two-year R34 treatment development grant is to develop a mobile health (mHealth) application that will both advance theory in and clinical practice of homework (HW) implementation.
HW can be described as between-session exercises where the client practices specific skills learned within-session in order to promote skill acquisition, which ultimately leads to improved acute- as well as longer-term therapeutic benefits on targeted outcomes, generalization of treatment effects and maintenance of treatment gains. Despite data demonstrating that HW is critical to achieving maximal benefits from evidence-based treatments, very little theory-driven approaches have been conducted focusing on improving the HW process. Through utilizing self-determination theory as a guiding framework and integrating principles from the field of "gamification" and goal-setting, the aim is to develop a two-component mHealth HW application (My MFG).
The first component focuses on delivering HW via a highly engaging, multiplayer, interactive, cooperative, and skill-building game platform aimed at improving the "Design" and "Do" process of HW. The second component focuses on targeting factors putatively related to poor HW implementation within the "Do" process.
The process of the development of My MFG will be guided by the clinic and community development model and iterative software development process to maximize the feasibility and sustainability of My MFG within practice settings often characterized by limited resources. Findings from this study have broad implications for evidence-based treatments for youth and adult mental health disorders that emphasize HW as the link between treatment and improvements in targeted outcomes.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The aim of the proposed study is to develop a theory-informed mobile health (mHealth) application for urban caregivers attempting to improve their children's oppositional and conduct related difficulties (i.e., disruptive behavior disorders; DBDs). The majority of evidence-based treatments (EBTs) targeting youth DBDs emphasize change in specific parenting/family-level processes empirically linked to the maintenance of DBDs. Existing EBTs frequently include at-home-practice-exercises (i.e., homework; HW) to reinforce parent skill acquisition and maximize use of new skills with children at home. Poor quantity and quality of HW completed by parents significantly attenuates the effect of EBTs. This is a significant limiting-factor in many EBTs attaining full public health impact. Given the robust effect of HW on outcomes from EBTs across a range of behavioral health difficulties and populations, there is a call for moving beyond the question of whether HW is important to questions such as what processes are involved in HW implementation and how best to support these processes. Minimal investigation has been focused on these critical questions.
A model of HW has recently been proposed to better understand the process of HW implementation, as well as guide critically needed supports for at-home practice exercises.
This model proposes four HW processes:
- Designing;
- Assigning;
- Doing, and;
- Reviewing.
The DADR model proposes that specific social, cognitive and behavioral factors related to the HW task, as well as to the provider and the adult caregiver may affect the quality of each phase and ultimately to the quantity and quality of HW completed. Methods to better understand, support, and impact these processes are essential to advancing theory and offering solutions to HW completion.
Through features available on smartphones (e.g., camera/video/voice recording; simple message service; internet-access; global positioning system), there are novel methods to interface with and support clients outside of defined treatment sessions. Through the use of these features, mHealth applications can be used to engage, educate, connect, track, and remind clients. These applications can use push (send communications) or pull (client's access tools on their own) mechanisms to engage the client in behavioral change activity. mHealth applications that integrate push and pull methods offer a significant opportunity to enhance outcomes across a range of health and behavioral health challenges and populations.
The goal of this two-year R34 treatment development grant is in response to RFA-MH-13-061 (Harnessing advanced health technologies to drive mental health improvement) to develop a mHealth application that will both advance theory in and clinical practice guided by the DADR model of HW implementation. Specifically we aim to utilize mHealth to improve the "Design" and "Do" process of HW within the context of the Family Groups for Youth with Behavioral Difficulties (MFG) intervention, an EBT for DBDs in youth and their families who seek assistance at outpatient mental health clinics in urban communities. To date, efforts at utilizing mHealth within the context of HW have been minimal and have not taken a systematic, theory-driven approach, thereby limiting the advance of knowledge and clinical application. Through utilizing self-determination theory as a guiding framework and integrating principles from the field of "gamification" and goal-setting, the aim is to develop a two-component MFG mHealth HW application (My MFG). The first component focuses on delivering MFG HW via a highly engaging, multiplayer, interactive, cooperative, and skill-building game platform aimed at improving the "Design" and "Do" process. The second component focuses on targeting factors putatively related to poor HW implementation within the "Do" process.
The process of the development of My MFG will be guided by the clinic and community development model and iterative software development process to maximize the feasibility and sustainability of My MFG within practice settings often characterized by limited resources. The specific aims of this project are to:
- Develop My MFG through an iterative process informed by the perspectives of key stakeholders
Determine the impact of MFG plus My MFG relative to MFG-alone on the DADR process and HW quantity and quality. It is hypothesized that the MFG plus My MFG will result in:
- Greater quality of the "Design" and "Do" process rated by therapists, parents, and independent coders
- Greater quantity and quality of HW assignments rated by therapists and parents
- Greater quality of the "Review" process as rated by therapists, parents, and independent coders as a function of improved HW quantity and quality
- Greater satisfaction with treatment as rated by the parent, target child, and therapists NIMH has specifically called for acceleration of research to maximize the ability of current treatments to reduce symptoms, improve adherence and functioning while improving quality of and lowering the cost of care. The mHealth application and methods proposed herein serve as systematic, theory-driven approaches to significantly advance understanding of how best to support the HW process-a common element of many EBTs across various disorders and populations-ultimately resulting in greater effectiveness of EBTs, maintenance and generalization of behavioral skills learned during EBTs.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New York
-
New York, New York, United States, 10003
- McSilver Institute for Poverty Policy and Research - New York University Silver School of Social Work
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
1) youth between the ages of 7 to 13 years and an accompanying adult primary caregiver available to participate in the research and intervention activities 2) English speaking youth and adult caregiver and 3) youth meeting criteria for DBD via parent reports based on the Disruptive Behavior Disorder (DBD) rating scales of DSM symptoms and cross-situational impairment as assessed through parent ratings on the Impairment Rating Scale (IRS). Children will be diagnosed with DBD if they meet DSM symptom criteria for DBD by parent report (i.e., at least four symptoms of ODD or 3 symptoms of CD), and impairment ratings indicate at least one impairment domain.
-
Exclusion Criteria:
Children will also be excluded if there is:
- Evidence of psychosis
- If the youth or adult caregiver presents with emergency psychiatric needs that require services beyond that which can be managed within an outpatient setting (e.g. hospitalization, specialized placement outside the home), active intervention by clinic and research staff to secure what is needed will be made
- Children will not be excluded if they participate in other psychosocial or pharmacological interventions.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MFG plus MyMFG
MFG plus MyMFG will be tested and the aim is:
|
Specific aim is to utilize mHealth to improve the "Design" and "Do" process of HW within the context of the Family Groups for Youth with Behavioral Difficulties (MFG) intervention, an EBT for DBDs in youth and their families who seek assistance at outpatient mental health clinics in urban communities. The first component focuses on delivering HW via a highly engaging, multiplayer, interactive, cooperative, and skill-building game platform aimed at improving the "Design" and "Do" process of HW. The second component focuses on targeting factors putatively related to poor HW implementation within the "Do" process. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
DADR Process- HW quantity and quality, Homework Rating Scale-II
Time Frame: Weekly for 16 weeks; duration of group
|
This assessment helps to understand the DADR process and to assess if homework was completed and how much.
|
Weekly for 16 weeks; duration of group
|
|
DADR Proces- Homework Adherence and Competence Scales
Time Frame: Participants will be tracked up to 16 weeks and feedback will be collected every week.
|
An independent observer will assess level of homework adherence and competence in every session.
|
Participants will be tracked up to 16 weeks and feedback will be collected every week.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
DBD Symptoms -DBD Rating Scale
Time Frame: Day 1- 1st contact
|
To assess the severity of behavior problems.
|
Day 1- 1st contact
|
|
Children's Impairment Rating Scale
Time Frame: Day 1- 1st Contact
|
To assess level of behavioral impairment for child- caregiver reports.
|
Day 1- 1st Contact
|
|
Attendance
Time Frame: Weekly- duration of the 16 week group
|
Attendance will be measured for each participant at every session.
|
Weekly- duration of the 16 week group
|
|
IOWA Conners Oppositional/Defiant Scale
Time Frame: 1st contact and at the end of the 16 week group
|
Caregiver assesses child's oppostitional and defiant behaviors at pre and post treatment.
|
1st contact and at the end of the 16 week group
|
|
Consumer Satisfaction & Feedback- Treatment Attitude Inventory
Time Frame: 1st contact and at the end of the 16 week group
|
This is a feedback assesment that will happen at either group or individual consultancy meeting to assess feedback of the MHealth process by parent, target child, and therapist.
|
1st contact and at the end of the 16 week group
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Mary M McKay, PhD, New York University Silver School of Social Work
- Study Director: Tyrone M Parchment, LMSW, New York University Silver School of Social Work
- Study Director: Ozge Sensoy-Bahar, PhD, New York University Silver School of Social Work
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- R34MH100407-01 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Mental Health Wellness 1
-
Indiana UniversityCommunity Health Network; Boys & Girls Clubs of IndianapolisCompletedMental Health Wellness 1 | Child Behavior | Adolescent Behavior | Mental Health Wellness 2United States
-
Cedars-Sinai Medical CenterNot yet recruitingMental Health Wellness 1 | Wellness, PsychologicalUnited States
-
King's College LondonCompletedMental Health Wellness 1 | Mental Health IssueUnited Kingdom
-
Universiti Putra MalaysiaGreen International UniversityNot yet recruitingMental Health Wellness 1
-
Northern Arizona UniversityUniversity of Colorado, DenverRecruiting
-
The New SchoolColumbia University; Universidad del Norte; HIASRecruitingMental Health Wellness 1Colombia
-
University of Wisconsin, MadisonCompletedMental Health Wellness 1United States
-
University of BathKing's College London; University of Pennsylvania; Newcastle University; University... and other collaboratorsCompletedMental Health Wellness 1United Kingdom
-
The University of Hong KongThe Boys' and Girls' Clubs Association of Hong KongCompleted
-
University of South WalesMIND CymruTerminated
Clinical Trials on MFG plus MyMFG
-
Washington University School of MedicineNational Institute of Mental Health (NIMH)Active, not recruiting
-
Washington University School of MedicineNational Institute of Mental Health (NIMH)Active, not recruiting
-
University of ArizonaInstitute for Mental Health ResearchCompletedSchizophrenia | Schizoaffective Disorder | Major Depression With Psychotic Features | Bipolar Disorder With Psychotic Features | Psychotic Disorder Not Otherwise Specified (NOS) | Recent-Onset PsychosisUnited States
-
NYU Silver School of Social WorkCompleted
-
Icahn School of Medicine at Mount SinaiNational Institute of Mental Health (NIMH)CompletedConduct Disorder | Oppositional Defiant DisorderUnited States
-
Washington University School of MedicineNational Institute of Mental Health (NIMH)Completed
-
Washington University School of MedicineNational Institute of Mental Health (NIMH); New York University; University of... and other collaboratorsCompletedComparison Group | Multiple Family Groups by Parent Peers | Multiple Family Groups by Community Health WorkersGhana, Uganda, Kenya, United States
-
Washington University School of MedicineNational Institute of Mental Health (NIMH)Completed
-
VA Office of Research and DevelopmentCompletedDepression | Posttraumatic Stress Disorders | Mild Traumatic Brain InjuryUnited States
-
Yale UniversityCompletedSchizophrenia and Disorders With Psychotic FeaturesUnited States