- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07698860
Awareness Of Home Accident Preventıon Among Parents Of Disabled Children And Evaluation Of The Basic First Aid Training Provided
This study was conducted to assess the awareness of parents of children with disabilities regarding the prevention of home accidents and the effectiveness of the basic first aid training provided. A randomized controlled experimental study design with a pre-test-post-test format was employed to determine the effectiveness of home accident prevention awareness and basic first aid training provided to parents of children with disabilities attending special education schools. Research hypotheses:
Hypothesis 0: There is no significant difference between the pre-training and three-month post-training evaluations (pre-test-post-test) of the home accident prevention awareness and basic first aid training provided to parents of children with disabilities.
Hypothesis 1: There is a significant difference between the pre-training and three-month post-training assessments (pre-test-post-test) of home accident prevention awareness and basic first aid training provided to parents of children with disabilities.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
-
Kayseri, Turquía (Türkiye)
- Kayseri University
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
• Be at least 18 years of age
- Be providing care for a child with a disability
- The child must be enrolled in a special education school
Exclusion Criteria:
• Refusing to participate in the study
- Withdrawing from the study
- Failing to complete the data collection form
Plan de estudios
¿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 |
|---|---|
|
Sin intervención: No training
The group that did not receive training
|
|
|
Experimental: Education
The group receiving training
|
Prevention of Household Accidents and Basic First Aid Training for Accidents
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in Total Home Accident Awareness and Basic First Aid Knowledge Score
Periodo de tiempo: Baseline and three months after the training
|
The primary outcome is the change in the total home accident awareness and basic first aid knowledge score from pre-test to post-test.
The total score is calculated from 34 common items: 18 items from the Home Accident Awareness Assessment Form and 16 items from the Basic First Aid Training Assessment Form.
Items are rated on a 5-point Likert scale (1=strongly disagree, 5=strongly agree), with higher scores indicating greater awareness and knowledge.
Items 5 and 11 of the awareness form and items 3, 5, and 13 of the first aid form are reverse-coded.
After reverse coding, item scores are summed to obtain a total score ranging from 34 to 170.
The change score is calculated as post-test minus pre-test; positive values indicate improvement.
Sociodemographic items and the additional post-test item on recent home accidents are analyzed descriptively and excluded from the total score.
|
Baseline and three months after the training
|
|
Occurrence of Home Accidents During the Three Months After Training
Periodo de tiempo: Three months after the training
|
The secondary outcome is whether the child experienced a home accident during the three months after training.
This will be assessed using one additional post-test item and analyzed descriptively as frequency and percentage.
This item will not be included in the total score or change score calculations.
|
Three months after the training
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Adeviye Çopur, Kayseri University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 69952
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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. .