N/A
N=70
Lifestyle Enhancement for ADHD Program
ADHD
Bottom Line
View on ClinicalTrials.gov: NCT03690674 ↗Enrolled (actual)
70
Serious AEs
0.0%
Results posted
Apr 2022
Primary outcome: Primary: Moderate to Vigorous Physical Activity (MVPA) — 53.1; 51.8 Moderate-Vigorous Minutes per day
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Lifestyle Enhancement for ADHD Program (Behavioral)
- Age
- Pediatric · 5+ yrs
- Sex
- All
- Sponsor
- Seattle Children's Hospital
- Primary completion
- Dec 2019
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Moderate to Vigorous Physical Activity (MVPA) |
53.1; 51.8 | — |
| PRIMARY Garmin Wear Time |
49.18 | — |
| PRIMARY Number of Facebook Posts |
7.91 | — |
| PRIMARY Number of Caregivers With Attendance at the Focus Group |
29 | — |
| SECONDARY Stop Signal Reaction Time (SSRT) Task Score |
240.4285714; 244.8214286 | — |
| SECONDARY Digit Span (DS) Task - Total Score |
9.9; 10.31 | — |
| SECONDARY Finger Windows (FW) Task |
— | — |
| SECONDARY Behavior Rating Inventory of Executive Function (BRIEF) |
71.7; 68.4 | — |
| SECONDARY Impairment Rating Scale (IRS) |
72.2414; 64.7586 | — |
| SECONDARY Alabama Parenting Questionnaire (APQ) |
23.3; 22.6 | — |
| SECONDARY Health Behaviors Survey |
13; 4; 7; 4 | — |
| SECONDARY Child's Sleep Habits Questionnaire (Pre-school and School-aged Children) |
47; 44 | — |
| SECONDARY Conners-3 Questionnaire |
78.71; 75.75; 74.89; 71.68; 69.21; 63.21 | — |
| SECONDARY Teacher Vanderbilt |
4.91; 3.61; 3.67; 2.64 | — |
Summary
The purpose of this study is to investigate if physical activity (PA) can increase in children with Attention Deficit/Hyperactivity Disorder (ADHD) using a modified behavioral management training (BMT) program.
Eligibility Criteria
Inclusion Criteria
- age 5-10 years
- ADHD diagnosis
- CGI-S rating >4 and 60 min/day of MVPA for at least 5 days per week
Data sourced from ClinicalTrials.gov (NCT03690674). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.