SURA'A Campaign for Stroke Awareness in Primary Health Care Centers (SURA'A)
1 de junio de 2026 actualizado por: aya ahmed, University of Baghdad
"Effectiveness of a One-Week Multifaceted SURA'A Consultation-Based Campaign on Stroke Awareness and Intention to Seek Help Among Adults in Primary Health Care Centers
This study aims to evaluate the effectiveness of a one-week multifaceted Stroke Urgency Recognition, and Action Awareness (SURA'A) consultation-based campaign in increasing stroke awareness and the intention to seek emergency medical help among adults.
The research will be conducted at primary health care centers to determine if this specific educational approach can improve the community's response to stroke symptoms.
Descripción general del estudio
Estado
Aún no reclutando
Condiciones
Intervención / Tratamiento
Descripción detallada
The study will employ a multifaceted campaign based on the SURA'A consultation framework over a period of one week.
Participants from primary health care centers will be involved to assess their baseline knowledge and intention regarding stroke.
Following the intervention, changes in their awareness levels and help-seeking intentions will be measured and analyzed.
This research is approved by the Research Ethical Approval Committee at the University of Baghdad, College of Nursing.
Tipo de estudio
Intervencionista
Inscripción (Estimado)
350
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Estudio Contacto
- Nombre: Aya A Ghayadh, Master
- Número de teléfono: +9647822204528
- Correo electrónico: ayah.ahmed2106m@conursing.uobaghdad.edu.iq
Copia de seguridad de contactos de estudio
- Nombre: Sadeq A AL-Fayyadh
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
- Adulto Mayor
Acepta Voluntarios Saludables
Sí
Descripción
Inclusion Criteria
Participants will be eligible if they:
Age
- Adults aged ≥18 years residing in Diwaniyah.
- Residence o Living in Diwaniyah communities for at least 6 academic months prior to the study.
Access to Primary Health Centers (PHCs)
- Attending in selected primary health centers where the SURA'A campaign will be implemented.
Cognitive ability
o Able to understand and answer the survey questions in Arabic.
- Consent o Willing to provide informed consent to participate in pre- and post- awareness intervention assessments.
Availability for follow-up
o Agree to participate in both baseline (pre-campaign) and follow-up (post-campaign) assessments.
Exclusion Criteria
Participants will be excluded if they:
- Have a previous confirmed diagnosis of stroke (to avoid bias in baseline awareness).
Severe cognitive impairment
- Have diagnosed dementia, severe mental illness, or cognitive impairment that prevents reliable responses.
Communication barriers
o Cannot communicate in Arabic or has severe hearing/speech impairment that prevents participation.
- Health professionals o Physicians, nurses, paramedics, or students of medical and health colleges (to avoid overestimation of awareness).
Temporary visitors
o Non-residents or individuals visiting Diwaniyah temporarily.
- Refusal or withdrawal o Decline to participate or withdraw at any stage of the study.
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: SURA'A Consultation-Based Campaign Group
This experimental group will participate in a one-week multifaceted SURA'A consultation-based campaign.
The intervention focuses on increasing stroke awareness and the intention to seek medical help among adults in primary health care centers through structured professional consultations and educational materials.
|
The intervention consists of a one-week multifaceted SURA'A consultation-based campaign. This campaign is designed to increase stroke awareness and the intention to seek help among adults attending Primary Health Care Centers. The multifaceted approach likely includes: Targeted Consultations: Providing direct information to participants regarding stroke symptoms and emergency protocols. Educational Outreach: Utilizing the SURA'A framework-which typically focuses on rapid response (Sura'a meaning "speed" in Arabic)-to emphasize the importance of time-sensitive medical intervention. Community Integration: Implementing the campaign within the primary care setting to reach a diverse adult population during their routine health visits. |
|
Sin intervención: Routine Health Education Group
Participants in this arm will receive the standard routine health education or conventional care regarding stroke awareness typically provided at the Primary Health Care Centers.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Stroke Action Test (STAT)
Periodo de tiempo: Baseline (before the campaign) and 1 week later (immediately after the campaign).
|
The Stroke Action Test (STAT) is a validated tool used to assess the participants' knowledge of stroke symptoms and their intended behavioral response (intention to seek help) when witnessing a stroke.
It consists of multiple scenarios or questions.
Scores are calculated based on correct identified actions, with higher scores indicating better knowledge and more appropriate intended response to stroke symptoms.
|
Baseline (before the campaign) and 1 week later (immediately after the campaign).
|
|
action/intention medical help-seeking sub-scale
Periodo de tiempo: Baseline (before the campaign) and 1 week later (immediately after the campaign
|
This sub-scale is a component of the Stroke Action Test (STAT).
It specifically measures the participants' behavioral intentions and their promptness in seeking medical emergency services (e.g., calling an ambulance) when recognizing stroke signs.
It presents various scenarios to evaluate whether the participant would take the correct life-saving action.
|
Baseline (before the campaign) and 1 week later (immediately after the campaign
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
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)
10 de junio de 2026
Finalización primaria (Estimado)
20 de enero de 2027
Finalización del estudio (Estimado)
10 de abril de 2027
Fechas de registro del estudio
Enviado por primera vez
4 de mayo de 2026
Primero enviado que cumplió con los criterios de control de calidad
4 de mayo de 2026
Publicado por primera vez (Actual)
11 de mayo de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
4 de junio de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
1 de junio de 2026
Última verificación
1 de junio de 2026
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 135 (Identificador de registro: Research Ethical Approval Committee, College of Nursing , University of Baghdad.)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
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. .