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An Gratitude Programme Based on Islamic Teaching for the Well-Being of Emerging Adults (SHUKR)

26 août 2026 mis à jour par: Bela Akhtar Hasan Khan, Lincoln University College

Development and Validation of an Islamic Integrated Gratitude Intervention for Enhancing Well-Being Among Pakistani Muslim Adults

Gratitude practices have been shown to improve well-being but nearly all the programs tested so far were designed without reference to Islamic understanding.

This study tests a month-long gratitude program built around the Islamic concept of shukr. Participants complete a short daily journal entry, watch a short video before each day, and attend 5 online group sessions across 4 weeks.

The content covers what Shukr (Islamic gratitude) means, how it is expressed towards Allah and towards other people, and how it works during difficult times.

Participants are Muslim emerging adults aged 18 to 29 from Pakistan. They are randomly assigned either to the experimental or control group. Well-being and gratitude are measured before the program, at the end of the program, and at a follow-up after three months.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Description détaillée

The intervention was developed following the Medical Research Council framework for developing and evaluating complex interventions (Skywington et al, 2021). Development drew on a systematic literature review and 2 qualitative studies and interviews. First, with Islamic scholars, which produced a model of shukr covering its theocentric foundation, its expression through heart, tongue, and limbs, its unconditional character, the virtue surrounding it, the humility it produces, and its social outworking. Second, the interviews with practitioners experienced in delivering psychological interventions, which produced design and safeguarding requirements.

Existing gratitude interventions show modest effects, and three limitations recur: gratitude directed at other people can produce a sense of indebtedness rather than appreciation; gratitude exercises perform poorly for people who are currently distressed because the exercise depends on identifying benefits; and interventions transported without cultural adaptation lose effect, particularly when adaptation stays at the surface rather than the emerging population's own framework for making sense of events.

The intervention addresses each of these: gratitude is directed towards Allah, who requires no repayment in kind; shukr is paired with Sabr (patience), which makes gratitude practicable during hardship rather than only after benefit. The daily practice is attached to an existing routine to support habit formation, and content is drawn from Quranic text and prophetic narration rather than from a single scholarly tradition.

The intervention structure: 26 journal entries across 4 weeks, which are accompanied by prerecorded videos (presenting the same teaching and prompt as the workbook) and five facilitated group live sessions delivered online.The first session proceeds before day 1 of journal entries; the remaining sessions fall roughly at the end of each week. Week 3 addresses gratitude during hardship and includes content on adversity, unanswered prayers, and difficult relationships. Participants are informed which days are there before a week begins and may skip any day without explanation.

Safeguards include explicit exclusion of abusive relationships from the content on difficult people, wording that does not require disclosure of private matters, an anonymous well-being check administered roughly mid-intervention, and a defined support and escalation procedures.

Type d'étude

Interventionnel

Inscription (Estimé)

160

Phase

  • N'est pas applicable

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:

  • Muslim adults aged 18-29 years (emerging adulthood)
  • Sufficient English literacy to read the workbook independently
  • Reliable internet access for online group sessions
  • Able to provide informed consent

Exclusion Criteria:

  • Currently receiving treatment for a severe mental health condition
  • Currently in acute crisis or experiencing active suicidal ideation
  • Currently on psychiatric medication
  • Bereavement within the past 6 months

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: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Shukr Intervention
Participants receive the Islamic integrated gratitude programme delivered over four weeks. This includes a daily journal entry guided by a workbook, alongside pre-recorded videos (before each journal day, presenting the same teaching and prompt as the journal entry), and five facilitated live online group sessions.
An Islamically integrated gratitude intervention delivered over four weeks, comprising daily journal prompts, pre-recorded videos, and five facilitated live online group sessions.
Autres noms:
  • Shukr
Aucune intervention: Waitlist Control
Participants complete the same outcome measures at the same time points but receive no intervention during the study period. They are offered the full SHUKR programme after the final follow-up assessment is complete.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Psychological Well-Being Assessed Using Ryff's Psychological Well-Being Scale (18-Item Version)
Délai: Baseline (before intervention) and immediately after the 30-day intervention and at a 3-month follow-up
Psychological well-being is assessed using the 18-item version of Ryff's Psychological Well-Being Scale. Items are rated on a 7-point scale from 1 (strongly agree) to 7 (strongly disagree). Items 1, 2, 3, 8, 9, 11, 12, 13, 17, and 18 are reverse-scored. The total score ranges from 18 to 126, with higher scores indicating greater psychological well-being. The scale assesses autonomy, environmental mastery, personal growth, positive relations, purpose in life, and self-acceptance.
Baseline (before intervention) and immediately after the 30-day intervention and at a 3-month follow-up

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Gratitude Questionnaire (Six Item Form)
Délai: Baseline (before intervention) and immediately after the 30-day intervention and at a 3-month follow-up
Gratitude is assessed using the six-item Gratitude Questionnaire-Six Item Form (GQ-6). Items are rated on a 7-point scale from 1 (strongly disagree) to 7 (strongly agree). Items 3 and 6 are reverse-scored. The total score ranges from 6 to 42, with higher scores indicating greater gratitude.
Baseline (before intervention) and immediately after the 30-day intervention and at a 3-month follow-up

Collaborateurs et enquêteurs

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

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 (Estimé)

1 septembre 2026

Achèvement primaire (Estimé)

1 octobre 2026

Achèvement de l'étude (Estimé)

1 février 2027

Dates d'inscription aux études

Première soumission

20 août 2026

Première soumission répondant aux critères de contrôle qualité

20 août 2026

Première publication (Réel)

24 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

27 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

26 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • LUC-IIGI-2026

Plan pour les données individuelles des participants (IPD)

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

NON

Description du régime IPD

Individual participant data will not be shared because participant consent did not include sharing data with other researchers.

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

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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