Parent coaching may help teens keep weight off

NCT ID NCT03851796

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

418 people

The number who actually took part.

Started

May 2019

Finished

Oct 2024

Lead sponsor

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

12 to 16 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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.

obesity disorder Pediatric Obesity

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Children's Hospital of Richmond at VCU Healthy Lifestyles Center

    Henrico, Virginia, 23239, United States

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