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Behavioural Intervention
Mobile Behavioral Parent Training for ADHD
N/A
Waitlist Available
Research Sponsored by Florida International University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, average of 10 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial develops a smartphone app to teach positive parenting techniques to caregivers of children with ADHD. It provides feedback in-the-moment to help parents use the strategies.
Who is the study for?
This trial is for parents or primary caregivers of children aged 7-12 who have been diagnosed with ADHD. The child must show impairment in homework performance, and the caregiver must be willing to participate and able to use a smartphone app at home.
What is being tested?
The study tests a mobile Behavioral Parent Training (mBPT) app that teaches positive parenting through videos and quizzes. Caregivers are randomly assigned to either use the mBPT app alone or with added personalized phone prompts targeting their parenting behavior.
What are the potential side effects?
Since this trial involves educational content delivered via an application without medical interventions, there are no direct physical side effects expected from participating in this study.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, average of 10 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, average of 10 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Intervention Engagement
Receipt of Prompts
Secondary study objectives
Passive Audio Data- Positive Parenting
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: mBPT and just-in-time adaptive interventionExperimental Treatment2 Interventions
Group II: mBPT onlyActive Control1 Intervention
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Who is running the clinical trial?
Florida International UniversityLead Sponsor
106 Previous Clinical Trials
18,890 Total Patients Enrolled
17 Trials studying Attention Deficit Hyperactivity Disorder (ADHD)
2,391 Patients Enrolled for Attention Deficit Hyperactivity Disorder (ADHD)
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Eligibility Criteria:
This trial includes the following eligibility criteria:- Not applicable.I am between the ages of 7 and 12.My caregiver can join and access the treatment from home using a smartphone.
Research Study Groups:
This trial has the following groups:- Group 1: mBPT only
- Group 2: mBPT and just-in-time adaptive intervention
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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