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Anorexia Prevention in Female College Students

24 de junho de 2026 atualizado por: 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.

Visão geral do estudo

Descrição detalhada

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.

Tipo de estudo

Intervencional

Inscrição (Real)

135

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Gaungdong
      • Guangzhou, Gaungdong, China
        • Jinan University

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Sim

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Prevenção
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Dobro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: 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.
Comparador Ativo: 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.
Comparador Ativo: 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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Eating Disorder Risk
Prazo: 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
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Depressive Symptoms
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de junho de 2025

Conclusão Primária (Real)

1 de dezembro de 2025

Conclusão do estudo (Real)

1 de dezembro de 2025

Datas de inscrição no estudo

Enviado pela primeira vez

24 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

24 de junho de 2026

Primeira postagem (Real)

30 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

30 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

24 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

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.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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