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NCT07176234Enrolling by invitation

The LEADS Trial (Linking Exericise for Advancing Daily Stress Management)

Linking Exericise for Advancing Daily Stress (LEADS) Management and Resilience in African American Families

Source: ClinicalTrials.gov · Last updated 9 Jun 2026

Brief summary (registry, in English)

Chronic stressors have wide-reaching harmful effects on the physical, social, and psychological well-being of many African American (AA) families. These stressors place some AA adolescents, who already experience low rates of physical activity (PA) and high rates of obesity, at even greater risk for developing chronic diseases. Previous family-based interventions have targeted PA, diet, and sedentary behaviors to prevent and manage overweight and obesity, but few have been successful for AA adolescents. The investigators propose that this may be because chronic stressors are a major challenge to engagement in health promotion efforts, which has been significantly overlooked in previous interventions for AA families. Resilience-based interventions that empower youth to cope with daily stressors have shown improvements across a broad range of outcomes including mental health, academic achievement, and risk-taking behaviors. However, no previous study has evaluated a family-based stress and coping plus positive parenting intervention on improving engagement in PA in AA families. The Linking Exercise for Advancing Daily Stress (LEADS) Management intervention integrates a family-based intervention to address chronic stressors to promote behavioral skills for increasing PA in overweight AA adolescents and their parents. Based on Lazarus and Folkman's Stress and Coping Model, Family Systems, and Social Cognitive Theories, the proposed intervention integrates components that build coping skills (mindfulness, deep breathing, active coping, cognitive reframing), self-esteem (self-affirmation), and positive parenting practices (parent support, nurturance, family routines). The investigators propose that these protective factors as integrated into the LEADS intervention will buffer the negative effects of chronic stressors, which will lead to greater improvements in PA. The investigators pilot research indicates that the LEADS family-based intervention was feasible and acceptable and led to increased moderate-to-vigorous PA (MVPA) for adolescents. Thus, the primary aim of this study is 1) to evaluate the efficacy of the LEADS intervention on increasing MVPA from baseline to post-intervention, and maintenance at a 6-month follow-up in overweight AA adolescents. Secondary aims will examine 2) the effect of the LEADS intervention on light PA, dietary intake, family mealtime, body mass index, waist circumference, and blood pressure outcomes, 3) the effects of the intervention on parent outcomes, as well as examining 4) mediators of the intervention effect on changes in PA.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
330 (estimated)
First submitted
8 Sept 2025
Start date
25 Jan 2025
Primary completion date
10 Aug 2029
Lead sponsor
University of South Carolina
Diseases
Obesity
NCT number
NCT07176234

What you commit to

  • Study type: Interventional
  • Planned participants: 330
  • From 25 Jan 2025 to the primary completion date, 10 Aug 2029
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • criteria will include having a cardiovascular or orthopedic condition that would limit physical activity

Other

  • having limitations that would prevent physical activity, and for caregivers,
  • uncontrolled blood pressure.

Who the study is looking for

  • adolescent BMI greater than or equal 70th percentile;
  • self-identified African American or Black adolescents 11-16 years;
  • at least one parent/caregiver participating;
  • not currently in a structured physical activity, weight loss program or stress management program
  • access to the internet in his/her home.

Age in the registry: 11 years to 16 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of South Carolina
Coordinator of this site? Confirm its status
ColumbiaUnited StatesUnknown status
M.H. Newton Family Life Enrichment Center
Coordinator of this site? Confirm its status
SumterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.