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临床试验/NCT04694729
NCT04694729Unknown不适用

Comparison of the Effectiveness of Different Telerehabilitation Approaches in Chronic Obstructive Pulmonary Patients

Saglik Bilimleri Universitesi1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2021年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
54
试验地点
1
主要终点
Pulmonary function testing

研究概览

简要总结

Pulmonary rehabilitation (PR) is a first-line management strategy in chronic obstructive pulmonary patients (COPD) as it reduces shortness of breath, increases exercise capacity, and improves health-related quality of life. However, 8-50% of patients referred to PR do not participate at all, while 10-32% of those who start do not complete the program. Barriers to participation and completion include difficulty in accessing the program, poor mobility, lack of transport, and travel costs. Telerehabilitation is defined as the provision of rehabilitation services through telecommunication technology, including telephone, internet and video conference communications between the patient and the healthcare provider. Different technologies (from phone to video conferencing) have been tested in patients with COPD to enhance daily activities, exercise training and walking prescription. All of them showed positive effects on exercise tolerance, dyspnea, physical activity and quality of life. However, there is no study about which telerehabilitation program is more effective on COPD patients. The aim of this study is to investigate which telerehabilitation approach is more effective in COPD.

研究设计

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

入排标准

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

入选标准

  • •Being diagnosed with COPD (FEV1 / FVC <70% in the stable phase of the disease)
  • •Age > 18 years old
  • •Have the ability to use a smartphone

排除标准

  • •Musculoskeletal disorders that limit exercise
  • •Dizziness, significant sensory or motor impairments, dementia or terminal illnesses that prevent education
  • •Serious comorbidities such as unstable heart disease, irregular diabetes, known malignant disease, any other disease that makes the patient unsuitable for participation in the study.
  • •Incompatible patient
  • •Severe vision or hearing impairment
  • •Unwillingness or inability to follow the protocol
  • •Have had a COPD exacerbation in the previous 6 weeks

研究组 & 干预措施

study group

Experimental

Videoconference-based

干预措施: videoconference-based (Other)

control group

Experimental

Video-based

干预措施: video-based (Other)

结局指标

主要结局

Pulmonary function testing

时间窗: 6 week

6 minute walk test(6MWT)

时间窗: 6 week

次要结局

  • Time Up and Go Test(6 week)
  • Copd Assessment Test(6 week)
  • Short Physical Performance Battery(6 week)
  • International Physical Activity Questionnaire-Short Form(6 week)
  • 30-Second Chair Stand Test(6 week)
  • Hospital Anxiety and Depression Scale(6 week)
  • St George's Respiratory Questionnaire(6 week)
  • Medical Research Council Scale(6 week)
  • Static Lung Volumes(6 week)

研究者

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

Nursima Bulut

Physiotherapist

Saglik Bilimleri Universitesi

研究点 (1)

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