Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05031611 · ClinicalTrials.gov registry record · NA

Intuitive Eating for Disordered Eating

A NA study, sponsored by Yeshiva University.

Completed
Registry status
NA
Development phase
123
Enrollment target

NCT05031611: Completed NA study, sponsored by Yeshiva University.

NCT05031611 is a NA study that has completed, run by Yeshiva University. The registered enrollment target is 123 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05031611, a NA study, has completed, sponsored by Yeshiva University.

COMPLETED
Registry status
NA
Development phase
123 participants
Enrollment target

Study Summary

Purpose: Research on intuitive eating is growing, but there are few interventions demonstrating the effect of learning to eat intuitively for people with disordered eating. Young women in particular are at high-risk for developing disordered eating. This study aimed to test the outcomes of a novel intuitive eating intervention for young women with disordered eating. Methods: This study is the first randomized controlled trial introducing intuitive eating to a sample of participants with disordered eating. Participants with current eating disorders were excluded from this study. Women (n=123) ages 18-30 with high levels of disordered eating participated in this study and were randomized to either a treatment (10-week web-based intervention) or control group (10-week waitlist).

Primary Outcome

Intuitive eating was measured by the Intuitive Eating Scale, 2nd edition (IES-2). Scores on this scale range from 1 to 5, with higher scores indicating greater levels of Intuitive Eating.

Interventions

  • BEHAVIORAL Intuitive Eating Treatment

Trial Details

FieldValue
Enrollment Target 123 participants
Start Date 2020-04-08
Est. Completion 2021-03-17
Phase NA
Yeshiva University

7 total trials

What the finished NCT05031611 record still lists

NCT05031611 is an interventional study that assigns participants to a tested intervention. The registered 123 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).

The record links to 0 conditions, and to 1 intervention - of which Intuitive Eating Treatment is the first listed.

NCT05031611 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05031611 about?

NCT05031611 is a clinical study titled "Intuitive Eating for Disordered Eating". Purpose: Research on intuitive eating is growing, but there are few interventions demonstrating the effect of learning to eat intuitively for people with disordered eating. Young women in particular are at high-risk for developing disordered eating. This study aimed to test the outcomes of a novel i...

What is the current status of trial NCT05031611?

This trial is currently completed. It is a NA study. The enrollment target is 123 participants. The study started on 2020-04-08. Estimated completion is 2021-03-17.

What interventions are being tested in trial NCT05031611?

The interventions under investigation include: Intuitive Eating Treatment (BEHAVIORAL).

Who is sponsoring clinical trial NCT05031611?

This trial is sponsored by Yeshiva University, which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05031611's enrollment target sits among peer trials

123 762nd of 2000 higher than 1,239 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05285891 · 123 participants · Phase 4

    Ocrelizumab Discontinuation in Relapsing Multiple Sclerosis

  • NCT05334368 · 123 participants · Phase 3

    Depemokimab in Participants With Hypereosinophilic Syndrome, Efficacy, and Safety Trial

  • NCT06088355 · 123 participants · NA

    Moderate Versus High Volume Light-Moderate Intensity Exercise for People With Moderate Parkinson's Disease

  • NCT06111131 · 123 participants · NA

    Ancora-SB Overtube Complete Positioning and Optical Visualization During Endoscopic Procedures

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05031611, the US trial registry maintained by the National Library of Medicine. NCT05031611 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.