Eating Disorders Trial, Recruiting (NCT05693896)

Eating Disorders Trial, Recruiting NCT05693896 Sponsor: University of North Carolina, Chapel Hill Condition: Eating Disorders

Printed from Voxsanity (voxsanity.com.au) — NCT05693896 — Data sourced from ClinicalTrials.gov. Verify directly with the trial site before attending. Not medical advice.

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Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

You are 18 years of age or older
Your body mass index (BMI) is 30 or higher, which is generally considered obese (confirm with trial site if unsure of your BMI)
You own and regularly use a smartphone that has Bluetooth capability
You experience at least one episode of binge eating (eating a large amount of food in a short time, feeling out of control) per week
You live or work within 30 miles of Kannapolis, NC
You complete the trial's screening questionnaire

Who may not be able to join:

You are currently pregnant
You are currently receiving treatment for substance abuse
You are currently taking part in another weight loss program
You have a history of anorexia (an eating disorder involving severely restricted eating)
You are currently purging (for example, making yourself vomit after eating)
You are currently receiving any kind of treatment for eating difficulties
You currently use intravenous (injected) drugs
You drink more than 4 alcoholic beverages per day

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.

Last synced 28 July 2026

This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Rachel Goode, PhD,MPH, University of North Carolina, Chapel Hill

Phone: 704-250-5085

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Voxsanity

Clinical trials and treatments, explained plainly · voxsanity.com.au

Date:

To: My Doctor

Re: Clinical trial enquiry

I am writing to enquire about the following clinical trial which may be relevant to my care:

Trial: NCT05693896

Sponsor: University of North Carolina, Chapel Hill

Phase: Not Applicable

Status: Recruiting

Condition: Eating Disorders

Trial contact: 704-250-5085

More information: https://clinicaltrials.gov/study/NCT05693896

Eligibility summary (AI generated)

Written by an AI model from the ClinicalTrials.gov eligibility criteria and checked on a sample basis. Please confirm against the original criteria.

Who might be able to join this trial:

You are 18 years of age or older
Your body mass index (BMI) is 30 or higher, which is generally considered obese (confirm with trial site if unsure of your BMI)
You own and regularly use a smartphone that has Bluetooth capability
You experience at least one episode of binge eating (eating a large amount of food in a short time, feeling out of control) per week
You live or work within 30 miles of Kannapolis, NC
You complete the trial's screening questionnaire

Who may not be able to join:

You are currently pregnant
You are currently receiving treatment for substance abuse
You are currently taking part in another weight loss program
You have a history of anorexia (an eating disorder involving severely restricted eating)
You are currently purging (for example, making yourself vomit after eating)
You are currently receiving any kind of treatment for eating difficulties
You currently use intravenous (injected) drugs
You drink more than 4 alcoholic beverages per day

Important: Always verify eligibility with the trial site directly before applying.

Access in Australia: A treatment being studied in a clinical trial is generally not yet listed on the PBS. Where a medicine is not approved or not available through a trial, the TGA Special Access Scheme may allow a doctor to access unapproved therapeutic goods for individual patients. See voxsanity.com.au/sas-navigator/ for a plain English explainer.

This information was sourced from ClinicalTrials.gov via Voxsanity (data last synced 28 July 2026). It is not medical advice. Please verify the trial's current status directly with the trial site before acting.

Trial details

Status

Recruiting

Phase

Not Applicable

Sponsor

University of North Carolina, Chapel Hill

Registry

ClinicalTrials.gov

Start date

15 January 2025

Est. completion

1 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Feasibility (Recruitment): Total Number of Eligible Adults Enrolled in the Study; Retention: Percentage of Participants Retained in the Study; Attendance: Percentage of Intervention Sessions Attended

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov