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Completed

NCT Number: NCT07677020

Anorexia Prevention in Female College Students

This study evaluated whether an acceptance-based embodied movement program can reduce eating disorder risk and body shape concerns in female college students at elevated risk. A total of 135 female undergraduate and graduate students were randomly assigned to one of three groups: acceptance-based embodied movement, functional fitness control, or psychoeducation. The intervention lasted 8 weeks, and outcomes were assessed at baseline, week 4, week 8, and 3-month follow-up. The main outcomes were eating disorder risk and body shape concern. Secondary outcomes included depression, anxiety, body image flexibility, functionality appreciation, and body surveillance.

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Key information

Age range

18 year–25 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Jinan University

Guangzhou, Gaungdong, China

About this study

This was a single-blind, three-arm, parallel-group randomized controlled trial conducted among female college students at elevated risk of eating disorders or body shape concerns. Participants were recruited from Jinan University and randomly assigned in a 1:1:1 ratio to acceptance-based embodied movement, functional fitness control, or psychoeducation.

The acceptance-based embodied movement program used low-impact mindful movements derived from yoga and tai chi and incorporated acceptance and commitment therapy techniques. The program emphasized present-moment body sensations, acceptance of appearance-related thoughts and feelings, cognitive defusion, valued action, and appreciation of body functionality. The functional fitness control program matched the movement intervention in session duration, frequency, and contact time, but removed mindfulness and acceptance components. It included aerobic and core exercises with standard fitness instruction. The psychoeducation program provided cognitive and dissonance-based body image education without physical activity.

All three programs lasted 8 weeks and were delivered in groups by trained facilitators using written manuals. Outcomes were assessed at baseline, mid-intervention, post-intervention, and 3-month follow-up. The primary outcomes were eating disorder risk measured by the Eating Disorder Examination Questionnaire Short Form and body shape concern measured by the Body Shape Questionnaire-8C. Secondary outcomes included depression, anxiety, body image flexibility, functionality appreciation, and body surveillance. Attendance, intervention fidelity, and adverse events were monitored throughout the study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female undergraduate or graduate students.
  • Aged 18 to 25 years.
  • Elevated eating disorder risk or body shape concern based on the prespecified screening threshold.
  • Physically able to participate in light-intensity physical activity.
  • Provided written informed consent.

Exclusion criteria

  • Current treatment for an eating disorder.
  • Any physical condition contraindicating participation in exercise.
  • Pregnancy.
  • Concurrent participation in another structured body image or exercise program.

Treatment and study plan

Acceptance-Based Embodied Movement

Behavioral

An 8-week group-based embodied movement program using low-impact mindful movements derived from yoga and tai chi. The program incorporated acceptance and commitment therapy techniques, including present-moment body awareness, acceptance of appearance-related thoughts and feelings, cognitive defusion, valued action, and appreciation of body functionality.

Functional Fitness Control

Behavioral

An 8-week group-based functional fitness program matched to the embodied movement program in session duration, frequency, and contact time. The program included aerobic and core exercises with standard fitness instruction and did not include mindfulness, acceptance, or body-image-focused guidance.

Psychoeducation

Behavioral

An 8-week group-based psychoeducation program without physical activity. The program provided cognitive and dissonance-based body image education, including critical discussion of idealized media images, appearance-focused talk, and body-related self-esteem.

Primary outcomes

  1. Eating Disorder Risk

    Time frame: Baseline, week 4, week 8, and week 20 follow-up

    Eating disorder risk was measured using the Eating Disorder Examination Questionnaire Short Form (EDE-QS). Higher scores indicate greater eating disorder risk.

  2. Body Shape Concern

    Time frame: Baseline, week 4, week 8, and week 20 follow-up

    Body shape concern was measured using the 8-item Body Shape Questionnaire (BSQ-8C). Higher scores indicate greater body shape concern.

Secondary outcomes

  1. Depressive Symptoms

    Time frame: Baseline, week 4, week 8, and week 20 follow-up

    Depressive symptoms were measured using the 9-item Patient Health Questionnaire (PHQ-9). Higher scores indicate more severe depressive symptoms.

  2. Anxiety Symptoms

    Time frame: Baseline, week 4, week 8, and week 20 follow-up

    Anxiety symptoms were measured using the 7-item Generalized Anxiety Disorder scale (GAD-7). Higher scores indicate more severe anxiety symptoms.

  3. Body Image Flexibility

    Time frame: Baseline, week 4, week 8, and week 20 follow-up

    Body image flexibility was measured using the Body Image Acceptance and Action Questionnaire (BI-AAQ). Higher scores indicate greater body image flexibility.

  4. Functionality Appreciation

    Time frame: Baseline, week 4, week 8, and week 20 follow-up

    Functionality appreciation was measured using the Functionality Appreciation Scale (FAS). Higher scores indicate greater appreciation of body functionality.

Sponsors and collaborators

Lead sponsor

Jinan University Guangzhou

Other

Registry information

Official study title

Prevention of Anorexia Nervosa in Female College Students

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jun 30, 2026
Registry last updated
Jun 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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