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临床试验/NCT04186754
NCT04186754已完成不适用

Interdisciplinary Randomized Study of an Integral Respiratory Rehabilitation Program in Oncological Patient With Disney

University of Salamanca1 个研究点 分布在 1 个国家目标入组 109 人开始时间: 2015年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
109
试验地点
1
主要终点
Dyspnoea

研究概览

简要总结

Hypothesis: Oncological patients presenting with respiratory problems will benefit both at a functional level and at a level of quality of life from the inclusion of a program of integral respiratory rehabilitation from the perspective of nursing and occupational therapy at the time of admission hospital for an exacerbation of his respiratory symptoms.

Main objective: to verify the effectiveness of a comprehensive respiratory rehabilitation program carried out from the perspective of an interdisciplinary team made up of nurses, occupational therapists and doctors in the improvement of the respiratory problem referred to oncological disease.

Design: experimental, randomized, stratified, longitudinal prospective study through a parallel scheme of fixed assignment with experimental group and control group.

详细描述

Hypothesis: Oncological patients presenting with respiratory problems will benefit both at a functional level and at a level of quality of life from the inclusion of a program of integral respiratory rehabilitation from the perspective of nursing and occupational therapy at the time of admission hospital for an exacerbation of his respiratory symptoms.

Main objective: to verify the effectiveness of a comprehensive respiratory rehabilitation program carried out from the perspective of an interdisciplinary team made up of nurses, occupational therapists and doctors in the improvement of the respiratory problem referred to oncological disease.

Design: experimental, randomized, stratified, longitudinal prospective study through a parallel scheme of fixed assignment with experimental group and control group.

Location: Medical Oncology Service of the University Hospital of Salamanca.

PROCESS

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Have an anatomopathological diagnosis of cancer disease among the reasons for admission.
  • Present at least some level 2 or moderate dyspnea parameters on the MRC scale.
  • Be admitted to the University Hospital of Salamanca.
  • Sign an informed consent authorizing their voluntary participation in the study.

排除标准

  • Present a diagnosis of bone metastases.
  • Not having an adequate cognitive state to understand and carry out the orders provided.
  • Carry out a number of rehabilitation sessions of less than
  • Present hemoglobin levels below 10g / dl.
  • To be an active smoker today.
  • Present pleural effusion.
  • Present febrile neutropenia.

研究组 & 干预措施

Comprehensive functional care plan

Experimental

The intervention will be carried out thanks to the "reeducation to the effort" carried out in the individuals, which will have the following interventions:

The treatment should be carried out INDIVIDUALIZED, in the hospital room or in a conditioned room, in sessions of approximately 30 minutes and on a daily basis. Carried out by professionals in the disciplines of nursing and occupational therapy.

干预措施: Comprehensive functional care plan (Procedure)

Traditional intervention without rehabilitation

Active Comparator
  • Nursing care.
  • Medical care.
  • Spiritual attention.

干预措施: Traditional intervention without rehabilitation (Procedure)

结局指标

主要结局

Dyspnoea

时间窗: Up to 3 years

MRC scale

次要结局

  • Activities of Daily Living(Up to 3 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Dr. Eduardo J Fernández Rodríguez

Principal Investigator

University of Salamanca

研究点 (1)

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