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Web-based Acceptance and Commitment Therapy (ACT) Intervention for University Students

3 de setembro de 2026 atualizado por: National University of Modern Languages

Preliminary Effectiveness Study of Web-based Acceptance and Commitment Therapy (ACT) Intervention for Promoting Wellbeing in University Students

University students frequently experience psychological distress, reduced wellbeing, and academic challenges associated with the transition to higher education. This randomized controlled trial evaluated the effectiveness of a culturally adapted web-based intervention based on the principles of Acceptance and Commitment Therapy (ACT). Participants were randomly assigned to either an intervention group receiving an eight-session online mindfulness program or a wait-list control group. The intervention was designed to improve mindfulness, psychological flexibility, wellbeing, quality of life, and academic functioning. Outcomes were assessed using standardized self-report measures administered before and after the intervention. The study examined whether participation in the intervention resulted in significant improvements compared with the wait-list control condition.

Visão geral do estudo

Status

Concluído

Condições

Descrição detalhada

University students commonly encounter academic, social, and personal stressors that increase their risk of psychological distress and negatively affect wellbeing and academic performance. Although mindfulness-based interventions have demonstrated effectiveness in improving mental health outcomes, evidence regarding culturally adapted web-based interventions for Pakistani university students remains limited.

This study developed and evaluated a culturally appropriate web-based intervention grounded in the six core processes of Acceptance and Commitment Therapy (ACT), including acceptance, cognitive defusion, present-moment awareness, self-as-context, values clarification, and committed action. The intervention was delivered online over eight weekly sessions and included psychoeducation, mindfulness exercises, breathing practices, experiential activities, and home assignments.

A randomized controlled trial was conducted among undergraduate psychology students enrolled at the National University of Modern Languages (NUML), Islamabad. Participants were randomly allocated to either the intervention group or a wait-list control group. Standardized measures of mindfulness, psychological flexibility, wellbeing, quality of life, academic psychological capital, work engagement, and general psychological health were administered before and after the intervention to evaluate its effectiveness.

Tipo de estudo

Intervencional

Inscrição (Real)

176

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

    • Islamabad
      • Islamabad, Islamabad, Paquistão, 44000
        • National University of Modern Languages (NUML), Islamabad.

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:

Undergraduate university students enrolled at the National University of Modern Languages (NUML), Islamabad.

Aged 18 years or older. Able to read and understand English and Urdu (or the language used for the intervention and questionnaires).

Willing to participate and provide written informed consent. Able to access the internet and complete the web-based intervention activities.

Exclusion Criteria:

Participants currently receiving any psychological treatment or psychotherapy. Participants with a diagnosed psychiatric disorder that would interfere with participation.

Participants unable to complete the web-based intervention or study assessments.

Participants who did not provide informed consent.

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: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Web-Based ACT Intervention
Participants received an eight-session web-based Acceptance and Commitment Therapy (ACT) intervention designed to improve mindfulness, psychological flexibility, wellbeing, and quality of life
Participants received an eight-session web-based intervention based on the principles of Acceptance and Commitment Therapy (ACT). The intervention was delivered online and included psychoeducation, mindfulness meditation practices, breathing exercises, experiential activities, values clarification, acceptance and cognitive defusion exercises, present-moment awareness, self-as-context activities, committed action tasks, and weekly home practice assignments. Each session was designed to enhance mindfulness, psychological flexibility, wellbeing, and quality of life among university students
Sem intervenção: Wait-list Control
Participants were assigned to a wait-list control group and did not receive the intervention during the study period. They were offered the intervention after completion of the post-intervention assessment.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in mindfulness scores measured by the Five facet mindfulness questionnaire (FFMQ)
Prazo: Baseline and immediately post-intervention (8 weeks)
Mindfulness was assessed at baseline and immediately after completion of the eight-session web-based intervention.
Baseline and immediately post-intervention (8 weeks)
Change in Psychological Flexibility score measured by the Acceptance and action questionnaire (AAQ-II)
Prazo: Baseline and immediately post-intervention (8 weeks)
It was administered at baseline and immediately after completion of the eight-session web-based intervention.
Baseline and immediately post-intervention (8 weeks)
Change in wellbeing scores measured by the WHO-Five-Well-being Index
Prazo: Baseline and immediately post-intervention (8 weeks)
Wellbeing was assessed at baseline and immediately after completion of the eight-session web-based intervention.
Baseline and immediately post-intervention (8 weeks)

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Change in Quality of Life score measured by the WHOQOL
Prazo: Baseline and immediately post-intervention (8 weeks)
it was assessed at baseline and immediately after the intervention.
Baseline and immediately post-intervention (8 weeks)
Change in Academic Psychological Capital score measured by Academic Psychological Capital Questionnaire
Prazo: Baseline and immediately post-intervention (8 weeks)
Academic Psychological Capital was measured before and after the intervention.
Baseline and immediately post-intervention (8 weeks)
Change in Academic Engagement score measured by Utrecht Work Engagement Scale for students (UWES)
Prazo: Baseline and immediately post-intervention (8 weeks)
Academic engagement was assessed before and after the intervention. before and after the intervention.
Baseline and immediately post-intervention (8 weeks)
Change in Mental Health score measured by the General Health Questionnaire (GHQ-12)
Prazo: Baseline and immediately post-intervention (8 weeks)
Mental health scores were assessed before and after the intervention.
Baseline and immediately post-intervention (8 weeks)

Colaboradores e Investigadores

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

Investigadores

  • Cadeira de estudo: Asia Mushtaq, National University of Modern Languages, Islamabad

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)

15 de março de 2024

Conclusão Primária (Real)

10 de abril de 2024

Conclusão do estudo (Real)

19 de agosto de 2024

Datas de inscrição no estudo

Enviado pela primeira vez

1 de agosto de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

1 de agosto de 2026

Primeira postagem (Real)

10 de agosto de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

4 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

3 de setembro de 2026

Última verificação

1 de setembro de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

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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