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Lifestyle Enhancement for ADHD Program 2

Lifestyle Enhancement for ADHD Program (LEAP) Study 2

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04779333
Acronym
LEAP
Enrollment
88
Registered
2021-03-03
Start date
2020-09-09
Completion date
2023-04-28
Last updated
2023-05-06

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

Conditions

Attention Deficit Hyperactivity Disorder

Brief summary

The purpose of this study is to increase physical activity (PA) in children with ADHD using a novel, family-based intervention that promotes PA within the context of evidence-based behavioral management training (BMT) for caregivers, enhanced with mobile health (mHealth) behavior change strategies. Primary Objective: To evaluate the primary effects of a 9-week, family-based intervention (Lifestyle Enhancement for ADHD Program - LEAP) to promote PA in young children with ADHD Secondary: To evaluate secondary effects of the LEAP program on child ADHD symptoms and executive functioning

Detailed description

This is a randomized trial comparing the LEAP program to standard BMT for ADHD (without the enhanced focus on health behaviors, mHealth technology, or social media). Specifically, 80 families will be randomized to receive either LEAP or a standard BMT program based on Russell Barkley's Defiant Children intervention manual. Moderators (e.g., child sex, medication, BMI) and mediators (e.g., change in PA) will be analyzed as exploratory outcomes. Hypotheses being tested include: 1) LEAP will be successful in increasing PA in children with ADHD in the short-term and over a year, more so than standard BPT and 2) children randomized to LEAP will exhibit greater and more sustained improvement in clinical outcomes relative to standard BMT. If successful, the R33 phase will inform the development of a larger and longer, confirmatory trial.

Interventions

BEHAVIORALLEAP

LEAP will be delivered through the typical 9 weekly BMT group sessions lasting 90 minutes. Plus wrist worn activity tracker & facebook group.

BEHAVIORALStandard BMT

Weekly BMT groups sessions which follow the Barkley curriculum

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
Seattle Children's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Years to 10 Years
Healthy volunteers
Yes

Inclusion criteria

(child): * Age 6-10 years * ADHD diagnosis * CGI-S rating ranging from 4 to 7. * Child not wearing a wrist-worn activity tracker more than 50% of days in the past month Inclusion Criteria (caregiver): * One adult custodial caregiver (resides with the child at least 50% of the time) willing to participate in the study and complete baseline/follow-up measures * Caregiver able to complete forms in English * Caregiver owns a smart phone or similar Garmin compatible mobile device (e.g. iPod Touch) or willing to borrow iPod from study coordinators during the study period * Agree to install and share data from the Garmin smart phone app with investigators Inclusion Criteria (supplementary caregiver): * An additional caregiver designated by the participating caregiver who provides care for the participating child on at least one occasion every other week * Able to participate in one or more group sessions * Able to consent in English

Exclusion criteria

(children): * \- Younger than 6 years old or older than 10 years old * Do not meet criteria currently for ADHD diagnosis * Meet diagnostic criteria for psychiatric co-morbidities of Autism Spectrum Disorder, Depressive Disorder, Mood Disorder, Psychotic Disorder, or Intellectual Disability (by history) * Per caregiver report, engage in \>60 min/day of MVPA consistently for at least 5 days per week * Any physical or medical restrictions on PA * Child currently/previously used a wearable physical activity sensing device at least 50% of days in the past month

Design outcomes

Primary

MeasureTime frameDescription
Effects of intervention on Physical ActivityBaseline to 10 weeksComparing within-subject pre to post activity (MVPA) using accelerometer data

Secondary

MeasureTime frameDescription
Effects of LEAP participation on child executive functionBaseline to 10 weeksEvaluate effects of LEAP participation on the child's executive functioning using the parent reported BRIEF-2 measure
Effects of LEAP participation on child ADHD symptomsBaseline to 10 weeksEvaluate effects of LEAP participation on the child's ADHD symptoms using the Conners-3 Parent Rating Scale

Countries

United States

Outcome results

None listed

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