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

3 settembre 2026 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Effettivo)

176

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

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

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

Sì

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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
Nessun intervento: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in mindfulness scores measured by the Five facet mindfulness questionnaire (FFMQ)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Quality of Life score measured by the WHOQOL
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: Baseline and immediately post-intervention (8 weeks)
Mental health scores were assessed before and after the intervention.
Baseline and immediately post-intervention (8 weeks)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Cattedra di studio: Asia Mushtaq, National University of Modern Languages, Islamabad

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

15 marzo 2024

Completamento primario (Effettivo)

10 aprile 2024

Completamento dello studio (Effettivo)

19 agosto 2024

Date di iscrizione allo studio

Primo inviato

1 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

1 agosto 2026

Primo Inserito (Effettivo)

10 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

4 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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