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Anorexia Prevention in Female College Students

24 juni 2026 bijgewerkt door: Xiaoma, Jinan University Guangzhou

Prevention of Anorexia Nervosa 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.

Studie Overzicht

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

135

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Gaungdong
      • Guangzhou, Gaungdong, China
        • Jinan University

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Preventie
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Dubbele

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Acceptance-Based Embodied Movement
Participants received an 8-week acceptance-based embodied movement program delivered in groups. The program used low-impact mindful movements derived from yoga and tai chi and incorporated acceptance and commitment therapy techniques, including present-moment awareness, acceptance of appearance-related thoughts and feelings, cognitive defusion, valued action, and appreciation of body functionality.
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.
Actieve vergelijker: Functional Fitness Control
Participants received an 8-week functional fitness control program delivered in groups. This program matched the embodied movement program in session duration, frequency, and contact time, but removed mindfulness and acceptance components. It included aerobic and core exercises with standard fitness instruction focused on exertion, completion of exercises, and cardiorespiratory fitness.
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.
Actieve vergelijker: Psychoeducation
Participants received an 8-week psychoeducation program delivered in groups 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.
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.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Eating Disorder Risk
Tijdsspanne: 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.
Baseline, week 4, week 8, and week 20 follow-up
Body Shape Concern
Tijdsspanne: 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.
Baseline, week 4, week 8, and week 20 follow-up

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Depressive Symptoms
Tijdsspanne: 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.
Baseline, week 4, week 8, and week 20 follow-up
Anxiety Symptoms
Tijdsspanne: 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.
Baseline, week 4, week 8, and week 20 follow-up
Body Image Flexibility
Tijdsspanne: 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.
Baseline, week 4, week 8, and week 20 follow-up
Functionality Appreciation
Tijdsspanne: 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.
Baseline, week 4, week 8, and week 20 follow-up

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

1 juni 2025

Primaire voltooiing (Werkelijk)

1 december 2025

Studie voltooiing (Werkelijk)

1 december 2025

Studieregistratiedata

Eerst ingediend

24 juni 2026

Eerst ingediend dat voldeed aan de QC-criteria

24 juni 2026

Eerst geplaatst (Werkelijk)

30 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

30 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

24 juni 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

Individual participant data will not be shared because participant consent and ethics approval did not include a plan for public sharing of individual-level data.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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