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临床试验/NCT05770505
NCT05770505已完成不适用

Effect E-health Based Exercise Intervention After COVID-19

Norwegian University of Science and Technology1 个研究点 分布在 1 个国家目标入组 77 人开始时间: 2023年4月17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
77
试验地点
1
主要终点
Cardiorespiratory fitness

研究概览

简要总结

Reduced subjective and objective functional capacity performance are reported after COVID-19 in a large proportion of subjects. The aim of this study is to examine the feasibility and effect of using an e-health tool for guidance and tracking of exercise training in a general population of adults previously infected by COVID-19.

详细描述

Both hospitalized and non-hospitalized persons who have undergone extensive multi-disciplinary rehabilitation programs report significantly improved physical function after rehabilitation. Exercise training may be the key intervention to improve fitness and subjective complaints such as fatigue, low physical fitness and dyspnea after COVID-19 infection. However, traditional group-based exercise training or self-training programs at fitness centers have been shut down during the pandemic, and home-based interventions are warranted. To overcome the limitations and costs of a fitness center/personal trainer-based intervention study, more knowledge on the effectiveness and efficacy of using an e-Health system to recruit, train and monitor participants after illness are needed.

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 59 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Persons who have undergone COVID-19 disease
  • •People who struggle to be physically active enough as a result of corona disease
  • •People who experience reduced physical fitness as a result of corona disease

排除标准

  • •-- more than 100 AQ per week (calculated from self-reported activity level)
  • •uncontrolled hypertension (high blood pressure) (over 200/110).
  • •symptomatic valve failure, hypertrophic cardiomyopathy, unstable angina, pulmonary
  • •hypertension, heart failure and/or severe rhythm disturbances
  • •cancer that makes participation impossible or exercise contraindicated. Considered individually in consultation with the attending physician.
  • •chronic contagious infectious diseases.
  • •Participates in other studies that are not compatible with participation in this project
  • •Post-exertional symptom exacerbation (PESE)/post-exertional malaise (PEM)/post-exertional neuroimmune exhaustion (PENE).

研究组 & 干预措施

Supervised exercise

Experimental

干预措施: Exercise training using an e-health tool (Behavioral)

Control group

No Intervention

结局指标

主要结局

Cardiorespiratory fitness

时间窗: After 6 months intervention

Peak oxygen uptake

Feasibilty

时间窗: After 6 months intervention

Measured as acceptability and adherence

次要结局

  • Lung function(After 6 months intervention)
  • Quality of life(After 6 months intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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