- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07663981
The Effect of Peer-Guided Education on Organ Donation on Organ Donation Attitude
18 de junio de 2026 actualizado por: Gülsüm ÖZCAN ÇETİNER, Suleyman Demirel University
This research will be conducted to determine the effect of peer-guided organ donation education given to anesthesia students on their attitudes towards organ donation.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Descripción detallada
There are many people waiting for organ donation in our country.
Therefore, it is important to develop a positive attitude towards organ donation in our society.
This study was planned to determine the effect of peer-guided organ donation education to be given to anesthesia students on the attitude towards organ donation.
In the study, anesthesia students will be informed about organ donation.
It was thought that the education given towards organ donation will develop a positive attitude in students.
Tipo de estudio
Intervencionista
Inscripción (Actual)
46
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.
Ubicaciones de estudio
-
-
Isparta
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Isparta, Isparta, Turquía (Türkiye), 32200
- Suleyman Demirel University
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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
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Sí
Descripción
Inclusion Criteria:
- Being 17 years of age or older, studying in the program in which the research is conducted, and agreeing to participate in the research voluntarily.
Exclusion Criteria:
- Having received prior training on organ donation
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: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Educational intervention
The educational intervention consists of a two-hour program prepared by the peer student in line with the literature.
The training session was planned to be completed in four sessions, with 30 minutes of session time.
These four sessions cover the traditional education model with the help of slide presentation.
The content of the training model was planned to use techniques such as participant activity, group work and discussion, and a brochure prepared by the researcher.
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The training on organ donation will be conducted under peer guidance.
The training will be implemented using face-to-face lectures, slide presentations, brochures and group discussions.
It will be conducted at Süleyman Demirel University in the 2025-2026 academic year for first-year anesthesia students.
The content of the training includes the concept of organ donation, the conditions for becoming a donor (physical, legal, religious), the social dimension of organ donation and attitude development sessions through group discussions.
The training, planned in four sessions, will last two hours in total.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in "Organ Donation Attitude Scale" Positive Attitude Sub-dimension Score
Periodo de tiempo: Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
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The Organ Donation Attitude Scale was originally developed by Parisi and Kanz (1986) and later adapted to 46 items by Kent and Owens (1995).
The Turkish validity and reliability study was conducted by Yazıcı Sayın (2016).
After removing items 6, 7, 12, 19, 27, and 45, the final version consists of 40 items rated on a 6-point Likert scale (from "strongly agree" to "strongly disagree") and includes two subscales.
TThe Positive Attitude Subscale of the Organ Donation Attitude Scale consists of 20 items assessing altruism and moral values and beliefs related to organ donation.
Each item is rated on a 6-point Likert scale.
The total subscale score ranges from 20 to 120.
Higher scores indicate a more positive attitude toward organ donation and therefore represent a better outcome.
Change in scores will be evaluated across the three assessment time points.
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Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
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Change in "Organ Donation Attitude Scale" Negative Attitude Sub-dimension Score
Periodo de tiempo: Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
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The Organ Donation Attitude Scale was originally developed by Parisi and Kanz (1986) and later adapted to 46 items by Kent and Owens (1995).
The Turkish validity and reliability study was conducted by Yazıcı Sayın (2016).
After removing items 6, 7, 12, 19, 27, and 45, the final version consists of 40 items rated on a 6-point Likert scale (from "strongly agree" to "strongly disagree") and includes two subscales.
The Negative Attitude Subscale of the Organ Donation Attitude Scale consists of 20 items assessing fear of medical neglect and fear of bodily injury related to organ donation.
Each item is rated on a 6-point Likert scale.
The total score ranges from 20 to 120.
Higher scores indicate a more negative attitude toward organ donation and represent a worse outcome.
Changes in the Negative Attitude Subscale score will be evaluated at baseline, immediately after the training program, and at the 1-month follow-up.
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Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in organ/tissue donation knowledge, awareness, and donation intention item scores
Periodo de tiempo: Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
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Participants' knowledge, awareness, and intention regarding organ/tissue donation were assessed using items included in the researcher-developed organ/tissue donation knowledge and attitude form.
These items evaluated participants' perceived level of knowledge about organ/tissue donation, knowledge of the required steps to become an organ/tissue donor, intention to donate organs/tissues, and perceived access to reliable sources of information about organ donation.
Each item was scored using Likert-type response options.
Higher scores indicated a more positive level of knowledge, awareness, or donation intention for the relevant item.
Changes in item scores were evaluated across the pre-test, post-test, and follow-up measurements.
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Baseline, immediately after completion of the 4-week training program (Week 4), and 1 month after completion of the training program (Week 8).
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Director de estudio: Gulsum OZCAN CETINER, Lecturer, Suleyman Demirel University
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 (Actual)
20 de noviembre de 2025
Finalización primaria (Actual)
11 de diciembre de 2025
Finalización del estudio (Actual)
25 de enero de 2026
Fechas de registro del estudio
Enviado por primera vez
3 de julio de 2025
Primero enviado que cumplió con los criterios de control de calidad
18 de junio de 2026
Publicado por primera vez (Actual)
23 de junio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
23 de junio de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
18 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
- 2025/95 (MTÜ Health Sciences Ethics Committee)
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. .