- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01785498
Healthy Lifestyles for Children With Complex Heart Problems (ReACH)
Healthy Lifestyles for Children with Complex Heart Problems is a planning and resource development project. The goal of the project is to develop an implementation plan that would enable children with complex heart problems to lead healthy, active lives within their own community. The primary goal of the project is to promote physical activity, because the physical and mental health benefits of activity are very important for these children. Children with complex heart problems have a higher risk for obesity, diabetes, acquired heart disease and mental health problems than their healthy peers. The physical health benefits of physical activity are well known, but physical activity is also key for children's mental health. Physical activity enables children to socialize with peers and create bonds and friendships. Physical activity participation also directly elevates mood through the release of brain chemicals. Children with complex heart problems are also known to experience fear and anxiety related to physical activity. This project will also develop strategies to promote healthy eating and the prevention of physical activity-related injuries to these children and their families. Children with complex heart problems are at higher risk of overweight and obesity and face unique injury risks related to pacemakers or their medications.
Extensive consultations with families and caregivers have identified needed supports for physical activity lifestyles, mental health, healthy eating and injury prevention for these children. The goal of the interviews was to understand the positive and negative influences on physical activity and healthy lifestyles for these children. Analyses of the interview content was used to develop a detailed, step-by-step implementation plan to provide the supports necessary for children with complex heart problems to lead active, healthy lives in their own community, with their family and friends. The implementation plan specifies changes to family education and counselling resources, clinical care routines, and communication among professionals and families.
The clinical trial will evaluate the impact of implementing the family supports and changes to practice previously developed. Surveys will be completed by families attending the cardiac clinic before and after the changes to practice and additional resources are made available. Interviews will be utilized to gather additional feedback from professionals and families that receive counselling utilizing the supplementary materials.
Descripción general del estudio
Estado
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Ontario
-
Ottawa, Ontario, Canadá, K1H 8L1
- Children's Hospital of Eastern Ontario
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- child with a heart condition requiring on-going follow up between 4 and 17 years of age or parent or healthcare provider of such a child
- able to verbally answer questions and express opinions in English or French
- able to provide informed consent or assent to participate
Exclusion Criteria:
- disability other than heart condition which significantly impacts physical activity participation or healthy lifestyle habits
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Sin intervención: Control Group
Receive standard clinical care and supports.
|
|
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Experimental: Supplementary resources
Receive standard care and supports plus supplementary resources developed for the intervention.
|
Clinical and educational resources for patients, their families and the professionals who care for them.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Family perception of clinical service
Periodo de tiempo: Within 2 weeks of clinic visit
|
Likert scales to measure family satisfaction with healthy lifestyle information and resources provided during clinic visit.
|
Within 2 weeks of clinic visit
|
|
Pediatric Quality of Life Inventory (PedsQL)
Periodo de tiempo: Within 2 weeks of clinic visit
|
Within 2 weeks of clinic visit
|
Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Change from Baseline of Children's Self-Perceived Adequacy and Predilection for Physical Activity
Periodo de tiempo: 1 month after intervention completion
|
1 month after intervention completion
|
Otras medidas de resultado
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Change from Baseline in Multi-dimension anxiety scale for children
Periodo de tiempo: 1 month after intervention completion
|
1 month after intervention completion
|
|
Change from Baseline in Pediatric Symptom Checklist
Periodo de tiempo: 1 month after intervention completion
|
1 month after intervention completion
|
|
Change from Baseline in PedsQL Family Impact Module
Periodo de tiempo: 1 month after intervention completion
|
1 month after intervention completion
|
Colaboradores e Investigadores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
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 (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
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
- REB12/04X
- 2012-06-1-4460033 (Otro número de subvención/financiamiento: Ministry of Health Promotion and Sport Healthy Communities Fund)
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. .