Fact CheckerSign in

NCT03851796Completed

Parent Involvement in Adolescent Obesity Treatment

The Role of Parents in Adolescent Obesity Treatment: Randomized Control Trial of TEENS+

Source: ClinicalTrials.gov · Last updated 12 Dec 2025

Brief summary (registry, in English)

A randomized control trial to compare the efficacy of two distinct parent treatments on weight loss maintenance for adolescents with obesity participating in a lifestyle intervention including nutrition education, exercise and behavioral support. Funding support from NIH via 1R01HD095910

Status (registry)
Completed
Study type
Interventional
Enrollment
418 (actual)
First submitted
12 Dec 2018
Start date
23 May 2019
Primary completion date
26 Oct 2024
Lead sponsor
Virginia Commonwealth University
Diseases
Obesity
NCT number
NCT03851796

What you commit to

  • Study type: Interventional
  • Participants enrolled: 418
  • From 23 May 2019 to the primary completion date, 26 Oct 2024
  • 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

  • Use of oral glucocorticoids, atypical antipsychotics, weight loss medications, or an investigational medication within 3 months of study participation
  • Previous participation in HM20010365, HM20003076, HM20005235 or HM20014304
  • Change in dose of metformin, tricyclic antidepressants, selective serotonin uptake inhibitors, or stimulant medications within 3 months of study participation
  • Use of oral glucocorticoids, atypical antipsychotics, weight loss medications, or an investigational medication within 3 months of study participation
  • Previous participation in HM20010365, HM20003076, HM20005235 or HM20014304

Other illness

  • Medical condition(s) that may be associated with unintentional weight change
  • Diabetes mellitus
  • Medical condition(s) that may be negatively impacted by exercise
  • Psychiatric, cognitive, physical or developmental conditions that would impair the ability to complete assessments, participate in a group, or conduct physical activity
  • Personal history of weight loss surgery
  • Clinically significant eating disorder
  • Admission to a psychiatric hospital within the past year
    • Parent Exclusion Criteria:
  • Medical condition(s) that may be associated with unintentional weight change
  • Psychiatric, cognitive, physical or developmental conditions that would impair the ability to complete assessments, participate in a group, or conduct physical activity
  • Personal history of weight loss surgery
  • Clinically significant eating disorder
  • Change in dose of diabetes medications, tricyclic antidepressants, selective serotonin uptake inhibitors, or stimulant medications within 3 months of study participation
  • Admission to a psychiatric hospital within the past year

Other

  • Adolescent Exclusion Criteria:
  • Non-English speaking
  • Use of a GLP-1 within 6 months of study participation
  • Use of Depo-Provera within 6 months of study participation
  • Reports of compensatory behaviors in the past 3 months
  • Current pregnancy or plan to become pregnant during study period
  • Current participation in another weight loss program
  • Severe depression
  • Non-English speaking
  • Use of a GLP-1 within 6 months of study participation with no T2D diagnosis; if T2D diagnosis, change in dose GLP-1 within 3 months of study participation
  • Use of Depo-Provera within 6 months of study participation
  • Reports of compensatory behaviors in the past 3 months
  • Current pregnancy, lactation, less than 6 months post-partum, or plan to become pregnant during study period
  • Current participation in another weight loss program
  • Severe depression

Who the study is looking for

  • Adolescent Inclusion Criteria:
  • BMI ≥ 85th percentile for age and gender according to the CDC Growth Charts
  • Age 12 to 16
  • Must reside with the primary participating parent
    • Parent Inclusion Criteria:
  • ≥18
  • BMI ≥ 25 kg/m2
  • Must reside with the adolescent

Age in the registry: 12 years to 16 years · Sex: All · Accepts 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
Children's Hospital of Richmond at VCU Healthy Lifestyles Center
Coordinator of this site? Confirm its status
HenricoUnited StatesUnknown status

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