Can a short online course tame binge eating? new study aims to find out
NCT ID NCT07435974
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a brief online program called COR for adults who struggle with binge eating. The program includes eight weekly sessions that teach skills to manage emotions and reconnect with eating in a healthy way. Researchers want to see if people find the program helpful and easy to stick with. About 30 adults will take part, and their feedback will guide future, larger studies.
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 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Jul 2026
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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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Adults aged 18 years or older. * Overweight or obesity, based on self-report. * At least three binge-eating episodes in the past 30 days, associated with psychological distress. * The presence of chronic medical conditions commonly associated with overweight or obesity (e.g., hypothyroidism, hyperthyroidism, dyslipidemia, hypertension, type 2 diabetes mellitus, or polycystic ovary syndrome) is permitted, provided that such conditions are medically stable. * If present, chronic medical conditions must be medically stable, defined as: * stable medical treatment for at least 12 weeks, * no recent changes in medication, * no acute clinical decompensation or recent major cardiovascular events, * at least one related medical follow-up visit in the past 12 months. * If present, psychopharmacological treatment must be stable, defined as no changes in medication type or dosage during the 12 weeks prior to enrollment. * Daily access to the internet and to a computer or smartphone that allows participation in online sessions and assessments. Exclusion Criteria: * Current compensatory behaviors associated with binge eating, such as self-induced vomiting and/or regular use of laxatives, within the past 60 days. * Pregnancy or breastfeeding at the time of the initial assessment. * History of bariatric surgery. * Active suicidal ideation * Current symptoms consistent with severe mental disorders, such as psychotic disorders, bipolar disorder, complex post-traumatic stress disorder, or severe personality disorders, when associated with marked functional impairment or the need for specialized or higher-intensity clinical care. * Current substance use pattern that, due to its severity or functional impact, requires specialized clinical treatment. * Ongoing psychological and/or nutritional treatment at the time of enrollment, defined as regular sessions or an active treatment plan, regardless of treatment focus or therapeutic approach. * Presence of active or medically unstable conditions, characterized by clinically significant symptoms, lack of medical follow-up, or recent changes in medication, that could interfere with participation in the intervention or substantially affect eating behavior or mood. * Significant functional impairment that, in the clinical judgment of the research team, would limit the participant's ability to engage safely and consistently in the intervention.
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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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Universidad Católica de Temuco
RECRUITINGTemuco, La Araucanía, 4780000, Chile
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Other studies related to the condition(s) this trial covers.
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