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NCT06969235Recruiting

Examining the Role of Executive Functioning in Family-Based Intensive Health Behavior and Lifestyle Treatment

Examining the Role of Executive Functioning in Family-Based Intensive Health Behavior and Lifestyle Treatment to Address Pediatric Obesity (Healthy LIFT Groups)

Source: ClinicalTrials.gov · Last updated 12 Feb 2026

Brief summary (registry, in English)

The objectives of this open trial feasibility study are to examine the impacts of intensive health behavior and lifestyle treatment (IHBLT) on youth and caregiver executive functioning (EF), weight status, health behaviors (dietary intake, disordered eating, physical activity), and psychological functioning. Investigators propose to enroll 10 youth 13 to 17 years of age who have overweight or obesity (OV/OB) and a primary caregiver. Families will receive six months of evidence-based family focused group IHBLT based on social, cognitive, and family systems theories. Families will complete assessments of EF skills (objective and self-report), weight status, dietary intake, physical activity, and psychological functioning at pre- and post-treatment.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
30 Apr 2025
Start date
5 May 2025
Primary completion date
Dec 2026
Lead sponsor
University of Missouri-Columbia
Diseases
Obesity
NCT number
NCT06969235

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 5 May 2025 to the primary completion date, Dec 2026
  • 1 site 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.

Prior treatment

  • Youth or caregiver in commercial weight loss program or taking prescribed medications for the prior three months that impact appetite or weight

Other illness

  • Youth pervasive developmental disorder (e.g., intellectual disability)
  • Youth or caregiver with documented history of eating disorder or untreated severe depression

Other

  • Both youth and caregiver scores are two standard deviations or above the mean on the CPT-3 Commissions and Stroop Interference, representing significantly higher than average EF skills.

Who the study is looking for

  • Youth 13-17 years old
  • Youth with OV/OB (BMI≥85th percentile for age/gender norms)
  • Participating caregiver must be the participating youth's legal guardian
  • Participating youth and caregiver speak and read English
  • Participating youth and caregiver agree to attend IHBLT group meetings in-between the pre- and post-treatment assessments.

Age in the registry: 13 years to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
College of Health Sciences, University of Missouri
Coordinator of this site? Confirm its status
ColumbiaUnited StatesRecruiting

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