- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT02938676
Satisfaction Degree in a Nurse Educational Program to Heart Transplant Patient
Satisfaction Degree With the Education Received in an Educational Program to Heart Transplant Patient During Hospitalization
Any member of the research team conducted screening for the selection of eligible patients. Nurses will be responsible for delivering the "Guide tips for the person with a transplanted heart", thus initiating an individualized education program. Education will be held at the time of admission in which the patient has passed the most critical post-operative.
Educational tips guide contains all the information necessary for the patient to have a first contact on the habits that must change. Education lasts 10-30 minutes and is taught in daytime, in a calm environment and at the right time, favoring the presence of the caregiver. Later, education is reinforced on the doubts that arise both the patient and the primary caregiver.
During the first days of admission to the unit of cardiology, socio-demographic data of the patient and primary caregiver by the research team will be collected.
A few days before discharge, having left time between 7-8 days after delivery of educational advice guide, any member of the research team, who does not work in the cardiology unit, will provide the patient and the primary caregiver the satisfaction questionnaire where the perception of information and education received during the postoperative period in the inpatient cardiology unit and the appropriateness of the topics covered in the guide educational advice.
Visão geral do estudo
Status
Condições
Descrição detalhada
- Conceptual Definition: Result of the difference between what the patient / caregiver expected to happen (patient expectations) and what claims to have obtained (their perception of the experience, the service provided) 14, 15.
Operational Definition: To assess the degree of satisfaction has designed a self-administered questionnaire specific for this study in which the following items were evaluated:
- Knowledge of the name and profession of the person performing the educational activity.
- Time used to provide educational session.
- Adequacy of time spent by nurses.
- At which has been given the educational session.
- Educational information received.
- Documentation provided.
- Understanding the information provided.
- Specific content by topics (general information, diet, hygiene measures, mood, exercise and cardiac rehabilitation, sexual activity, complications, skin, eye, gastrointestinal tract, bones, toxic habits, vaccination, contact other people, animals and plants, travel, employment high, associations heart transplant recipients).
- Satisfaction with education received
The overall satisfaction score is obtained from the sum of the scores of all items and a cut will be established from data obtained from median scores in a previous pilot survey conducted using 5 patients. The overall satisfaction score can range from 0 to 120 points.
Tipo de estudo
Inscrição (Antecipado)
Contactos e Locais
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Método de amostragem
População do estudo
Patients Unit hospitalization of Cardiology (B3) of the Hospital de la Santa Creu i Sant Pau (HSCSP) that during admission require surgery Heart Transplantation.
Convenience sampling in which eligible patients will be selected to participate in the study consecutively according to the time of admission to the inpatient
Descrição
Inclusion Criteria:
- Patients of both sexes, over 18 years.
- With medical diagnosis of heart transplant surgery during the same hospitalization.
- They must have a "primary caregiver" or a report favorable social support.
Exclusion Criteria:
- Medical diagnosis of cognitive impairment (Alzheimer's disease, senile dementia, neurological problem).
- Illiteracy and / or language barrier.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
---|---|---|
Patient satisfaction by a a self-administered questionnaire specific to this study
Prazo: 1 year
|
It will be evaluated:
|
1 year
|
Colaboradores e Investigadores
Investigadores
- Investigador principal: Alba Villalobos Abelló, Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
Conclusão Primária (Antecipado)
Conclusão do estudo (Antecipado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Estimativa)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Outros números de identificação do estudo
- IIBSP-SAT-2016-44
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .
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