Digital coaching may curb binge eating in black women with obesity
NCT ID NCT05693896
First seen Aug 10, 2026 · Last updated Aug 11, 2026 · Updated 1 time
Summary
This study tests a 6-month digital program that combines appetite awareness training with behavioral weight loss techniques, delivered remotely via Zoom. It aims to help Black women with obesity who binge eat at least once a week relearn hunger cues and prevent weight gain. The trial focuses on whether the approach is feasible and acceptable, measuring recruitment, retention, and attendance, along with changes in weight.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A digital behavioral program combining Appetite Awareness Training and behavioral weight loss, delivered via Zoom over 6 months.
- What this could lead to
- If successful, this could provide a scalable, culturally relevant digital treatment to reduce binge eating and prevent weight gain in Black women with obesity.
- What could go wrong
- This is a small feasibility study, so results may not generalize. It focuses on short-term outcomes and does not yet prove long-term effectiveness.
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
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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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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- 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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18 years and older
- Sex
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Female participants only
- 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: * Over 18 years of age with pre-diabetes, * Have an (A1c between 5.7%-6.4%), * BMI ≥ 30 kg/m\^2, * have and regularly use a Bluetooth-enabled smartphone, * report at least one binge eating episode weekly, * work or live within 30 miles of Kannapolis, NC, * Have not used prescription weight loss medications (like Wegovy, Zepbound, or Ozempic) in the past 3 months Exclusion Criteria: * currently pregnant, * Are currently taking or have taken within the prior 3 months (12 weeks) a GLP-1, * in substance abuse treatment, * involved in another weight reduction program, * have a history of anorexia, * are purging, * currently in treatment for eating difficulties, * are concurrent intravenous drug users * consume \>4 alcoholic beverages/day
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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UNC-Chapel Hill
Chapel Hill, North Carolina, 27599, United States
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