Exploring the Familial Reach of Adolescent Obesity Treatment

Sponsor
Virginia Commonwealth University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05780970
Collaborator
University of Connecticut (Other), University of North Carolina (Other), University of Tennessee (Other), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) (NIH)
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Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
60 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Exploring the Familial Reach of Adolescent Obesity Treatment
Actual Study Start Date :
Jan 1, 2022
Anticipated Primary Completion Date :
Mar 31, 2024
Anticipated Study Completion Date :
Jul 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Non-targeted individuals

Non-targeted children and caregivers living in the same household as the target parent/adolescent dyad. Non-targeted meaning they did not receive the TEENS+ intervention.

Other: No 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).

Outcome Measures

Primary Outcome Measures

  1. 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.

  2. Weight changes. [4 months (baseline to 4 months)]

    Weight changes observed among untreated individuals (child zBMI and caregiver % weight loss)

  3. 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
8 Years and Older
Sexes Eligible for Study:
All
Accepts 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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Children's Hospital of Richmond at VCU Healthy Lifestyles Center Henrico Virginia United States 23239

Sponsors and Collaborators

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

Investigators

  • Principal Investigator: Melanie K Bean, PhD, Virginia Commonwealth University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Virginia Commonwealth University
ClinicalTrials.gov Identifier:
NCT05780970
Other Study ID Numbers:
  • HM20014304 Phase 3
  • R21HD105906
First Posted:
Mar 23, 2023
Last Update Posted:
Mar 23, 2023
Last Verified:
Mar 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Virginia Commonwealth University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 23, 2023