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

3 septembre 2026 mis à jour par: 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.

Aperçu de l'étude

Statut

Complété

Les conditions

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Réel)

176

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

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

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Oui

La description

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.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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
Aucune intervention: 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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in mindfulness scores measured by the Five facet mindfulness questionnaire (FFMQ)
Délai: 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)
Délai: 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
Délai: 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)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change in Quality of Life score measured by the WHOQOL
Délai: 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
Délai: 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)
Délai: 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)
Délai: Baseline and immediately post-intervention (8 weeks)
Mental health scores were assessed before and after the intervention.
Baseline and immediately post-intervention (8 weeks)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chaise d'étude: Asia Mushtaq, National University of Modern Languages, Islamabad

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

15 mars 2024

Achèvement primaire (Réel)

10 avril 2024

Achèvement de l'étude (Réel)

19 août 2024

Dates d'inscription aux études

Première soumission

1 août 2026

Première soumission répondant aux critères de contrôle qualité

1 août 2026

Première publication (Réel)

10 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

4 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

3 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

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