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临床试验/NCT06579612
NCT06579612招募中不适用

The Benefits of Individualized Follow-up With a Sport-Health Professional in the Care of Patients With Chronic Respiratory Diseases, to Maintain Long-term Benefits After a Respiratory Rehabilitation Program

University Hospital, Brest4 个研究点 分布在 1 个国家目标入组 352 人开始时间: 2024年11月7日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
352
试验地点
4
主要终点
Difference in average number of daily steps

研究概览

简要总结

Pulmonary rehabilitation is an integral part of care for patients with chronic respiratory diseases. It improves patients' physical capacities, quality of life and symptoms, at least in the short term.

The hypothesis that patients receiving personalized support from a professional following pulmonary rehabilitation will maintain long-term benefits.

This study concerns patients with a diagnosis of one or more chronic respiratory diseases.

It is a multicenter, blinded, randomized controlled superiority trial in 2 parallel arms:

  • a group comparing follow-up and personalized support after a pulmonary rehabilitation program (experimental group)
  • a control group receiving only usual care

详细描述

Pulmonary rehabilitation is an integral part of care for patients with chronic respiratory diseases. It improves patients' physical capacities, quality of life and symptoms, at least in the short term.

The hypothesis that patients receiving personalized support from a professional following pulmonary rehabilitation will maintain long-term benefits.

This study concerns patients with a diagnosis of one or more chronic respiratory diseases.

It is a multicenter, blinded, randomized controlled superiority trial in 2 parallel arms:

  • a group comparing follow-up and personalized support after a pulmonary rehabilitation program (experimental group)
  • a control group receiving only usual care

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of one or more chronic respiratory diseases (asthma, chronic obstructive pulmonary disease, diffuse interstitial lung disease, bronchiectasis, obstructive sleep apnea syndrome, etc.).
  • Participation in a respiratory pulmonary program
  • Have given consent
  • Patient of legal age
  • Patient affiliated to Social Security

排除标准

  • Any medical contraindication to the practice of adapted physical activity in rehabilitation
  • Patients under guardianship or curatorship
  • Patients deprived of their liberty
  • Patients over 80 years of age at the time of inclusion.

研究组 & 干预措施

Control arm

No Intervention

Patient in the control arm will beneficiate from commun practice

Experimental arm

Experimental

Patient in the control arm will beneficiate from a personalized follow-up and support after a pulmonary rehabilitation program

干预措施: Personalized follow-up and support (Other)

结局指标

主要结局

Difference in average number of daily steps

时间窗: At inclusion (V1) and at 24 Months (V5)

The difference in average daily steps measured by accelerometry (over 7 days) at the end of the pulmonary rehabilitation course (V1) and after 24 months of personalized follow-up (V5).

次要结局

  • Cost-utility comparison between the two groups(At 24 Months (V5))
  • Comparison of changes in physical activity levels between the two groups(At 24 Months (V5))
  • Comparison of changes in physical capacities between the two groups(A 24 Months (V5))
  • Comparison of changes in symptoms between the two groups(At 24 Months (V5))
  • Comparison of changes in psychological dimensions between the two groups(At 24 Months (V5))
  • Comparison of changes in health indicator between the two groups(At 24 Months (V5))
  • Comparison of changes in quality of life indicator between the two groups(At 24 Months (V5))
  • Comparison of changes in parameters (barriers and levers to physical activity) between the two groups(At 24 Months (V5))
  • Comparison of changes in physical capacities between the two groups(At 24 Months (V5))
  • Cost-utility comparison between the two groups(At 24 Months (V5))
  • Comparison of changes in physical activity levels between the two groups(At 24 Months (V5))
  • Comparison of changes in symptoms between the two groups(At 24 Months (V5))
  • Comparison of changes in quality of life indicator between the two groups(At 24 Months (V5))
  • Comparison of changes in parameters (barriers and levers to physical activity) between the two groups(At 24 Months (V5))
  • Comparison of changes in psychological dimensions between the two groups(At 24 Months (V5))
  • Comparison of changes in health indicator between the two groups(At 24 Months (V5))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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