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

26 de agosto de 2026 actualizado por: 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.

Descripción general del estudio

Estado

Aún no reclutando

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

160

Fase

  • No aplica

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

Sí

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.
Otros nombres:
  • Shukr
Sin intervención: 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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Psychological Well-Being Assessed Using Ryff's Psychological Well-Being Scale (18-Item Version)
Periodo de tiempo: 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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Gratitude Questionnaire (Six Item Form)
Periodo de tiempo: 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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de octubre de 2026

Finalización del estudio (Estimado)

1 de febrero de 2027

Fechas de registro del estudio

Enviado por primera vez

20 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

20 de agosto de 2026

Publicado por primera vez (Actual)

24 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

27 de agosto de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

26 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • LUC-IIGI-2026

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

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

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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