Parent coaching may help teens keep weight off
NCT ID NCT03851796
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed study tested two ways parents can help teens with obesity maintain weight loss. 418 teens (ages 12-16) and their parents took part. One group focused on teaching parents coaching skills, the other on helping parents lose weight themselves. Both groups included teen weight management classes. The goal was to see which approach worked better for keeping weight off over a year.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- behavioral intervention (parent coaching and parent weight loss programs)
- What this could lead to
- If successful, this could show that involving parents in specific ways helps teens keep weight off long-term.
- What could go wrong
- This is a completed behavioral study, not a drug trial. Results may not apply to all families, and weight loss maintenance is challenging.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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418 people
The number who actually took part.
- Started
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May 2019
- Finished
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Oct 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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12 to 16 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 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 Exclusion Criteria: Adolescent Exclusion Criteria: * Non-English speaking * Medical condition(s) that may be associated with unintentional weight change * Diabetes mellitus * Use of oral glucocorticoids, atypical antipsychotics, weight loss medications, or an investigational medication within 3 months of study participation * Use of a GLP-1 within 6 months of study participation * Use of Depo-Provera within 6 months of study participation * 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 * Reports of compensatory behaviors in the past 3 months * Current pregnancy or plan to become pregnant during study period * Previous participation in HM20010365, HM20003076, HM20005235 or HM20014304 * Current participation in another weight loss program * Personal history of weight loss surgery * Severe depression * Clinically significant eating disorder * Change in dose of metformin, tricyclic antidepressants, selective serotonin uptake inhibitors, or stimulant medications within 3 months of study participation * Admission to a psychiatric hospital within the past year Parent Exclusion Criteria: * Non-English speaking * Medical condition(s) that may be associated with unintentional weight change * Use of oral glucocorticoids, atypical antipsychotics, weight loss medications, or an investigational medication within 3 months of study participation * 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 * Psychiatric, cognitive, physical or developmental conditions that would impair the ability to complete assessments, participate in a group, or conduct physical activity * 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 * Previous participation in HM20010365, HM20003076, HM20005235 or HM20014304 * Current participation in another weight loss program * Personal history of weight loss surgery * Severe depression * 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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Children's Hospital of Richmond at VCU Healthy Lifestyles Center
Henrico, Virginia, 23239, United States
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Other studies related to the condition(s) this trial covers.
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