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Exploring the Familial Reach of Adolescent Obesity Treatment

Exploring the Familial Reach of Adolescent Obesity Treatment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05780970
Enrollment
55
Registered
2023-03-23
Start date
2022-01-18
Completion date
2024-06-29
Last updated
2024-10-02

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

Conditions

Pediatric Obesity

Keywords

Pediatric Obesity, Lifestyle Intervention, Family-Level Change, Family-based Intervention

Brief summary

An observational study ancillary to the randomized clinical trial (RCT) TEENS+ (R01HD095910), a family-based lifestyle intervention, for adolescents with obesity, to determine: 1) if family-wide changes to the shared home environment are implemented, 2) if ripple effects to untreated family members are observed, and 3) whether these changes are predictive of adolescents' weight management success. Funding support from NIH via R21HD105906.

Detailed description

Investigators will recruit non-targeted children (8-17yrs) and caregivers living in the same household as the target TEENS+ parent/adolescent dyad. At 0, 2, 4 and 8m, the target adolescent/parent dyad (n=60), and non-targeted children and caregivers will complete anthropometric assessments, and measures of the shared home feeding and weight-related environment will be conducted.

Interventions

OTHERNo intervention

Non-treated children and caregivers complete assessments only. The primary (treated) parent / adolescent dyad participate in family based weight management treatment through the main trial. In the main trial, families are randomized to either TEENS+Parents as Coaches (parent skills training) or TEENS+Parent Weight Loss (parent behavioral weight loss).

Sponsors

University of Connecticut
CollaboratorOTHER
University of North Carolina
CollaboratorOTHER
University of Tennessee
CollaboratorOTHER
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
Virginia Commonwealth University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
8 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Untreated children: must be between 8-17 years of age and primarily living in the same household as the TEENS+ participants. * Untreated caregiver: must be 18 years of age or older and primarily living in the same household as the TEENS+ participants. * Treated caregivers: must have another individual in the household that meets the eligbility for an untreated child or untreated caregiver.

Exclusion criteria

* temporarily (\<1yr) living in the home * children with a BMI\<5th%ile or caregivers with a BMI\<18.5 kg/m2 * non-English speaking * medical condition(s) that may be associated with unintentional weight change or significant disruption to eating behaviors (e.g., hypothalamic injury, Prader-Willi, G-tube placement, or malignancy * clinically significant eating disorder (e.g., anorexia nervosa or bulimia nervosa) * following a medically-supervised/prescribed diet * psychiatric, cognitive, physical or developmental conditions that would impair the individual's ability to complete assessments.

Design outcomes

Primary

MeasureTime frameDescription
Family-level changes to the shared home environment.4 months (baseline to 4 months)Changes in the home food available and the home exercise and electronic media environment.
Weight changes.4 months (baseline to 4 months)Weight changes observed among untreated individuals (child zBMI and caregiver % weight loss)
Household changes and target adolescent weight.8 months [weight loss (baseline to 4 months) and maintenance (4-8)]Associations between household changes and target adolescent weight loss and maintenance.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026