跳至主要内容
临床试验/NCT05298878
NCT05298878已完成不适用

Virtual Physical Rehabilitation for Patients Living with Long COVID

McGill University Health Centre/Research Institute of the McGill University Health Centre4 个研究点 分布在 1 个国家目标入组 132 人开始时间: 2022年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
132
试验地点
4
主要终点
Change in the basic mobility domain of the Activity Measure for Post-Acute Care (AM-PAC)

研究概览

简要总结

The purpose of this study is to investigate whether a timely, virtual home-based physical rehabilitation program for patients living with long COVID can improve functional mobility compared to 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
Treatment
盲法
Single (Outcomes Assessor)

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

  • (i) adult patients (18+ years old) who have had a confirmed or probable COVID-19 infection and who have self-reported persisting symptoms of either reduced mobility, muscle weakness, dyspnea, or fatigue;
  • (ii) participants must be technologically capable of connecting (either independently or through household members) with an online videoconferencing platform through an e-mail invitation; and
  • (iii) be able to collaborate with the research assistant to complete the virtual assessment sessions or have a family member available to help.

排除标准

  • (i) pre-existing or newly identified severe cognitive impairment;
  • (ii) inability to speak or comprehend English or French;
  • (iii) known or self-reported acute and/or uncontrolled cardiac, musculoskeletal, or neurological condition that might render rehabilitation participation unsafe.

结局指标

主要结局

Change in the basic mobility domain of the Activity Measure for Post-Acute Care (AM-PAC)

时间窗: Baseline, Week 8 (up to 1 week), and at 6 months.

The AM-PAC is a validated, self-reported instrument assessing activity limitations based on the International Classification of Functioning, Disability, and Health (ICF). Each item is scored from 1 (unable to perform) to 4 (none or no difficulty) with lower scores indicating lower levels of function.

次要结局

  • Change in lower-body strength(Baseline, Week 8 (up to 1 week), and at 6 months.)
  • Change in anxiety and depression(Baseline, Week 8 (up to 1 week), and at 6 months.)
  • Change in health state utilities(Baseline, Week 8 (up to 1 week), and at 6 months.)
  • Self-reported health service use(30 days after the 8-week period.)
  • Change in cognitive function(Baseline, Week 8 (up to 1 week), and at 6 months.)
  • Change in the degree of distress in response to trauma(Baseline, Week 8 (up to 1 week), and at 6 months.)
  • Change in fatigue(Baseline, Week 8 (up to 1 week), and at 6 months.)
  • Change in health-related quality of life(Baseline, Week 8 (up to 1 week), and at 6 months.)
  • Change in functional mobility(Baseline, Week 8 (up to 1 week), and at 6 months.)
  • Change in dyspnea(Baseline, Week 8 (up to 1 week), and at 6 months.)

研究者

发起方
McGill University Health Centre/Research Institute of the McGill University Health Centre
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tania Janaudis-Ferreira

Scientist, Translational Research in Respiratory Diseases Program

McGill University Health Centre/Research Institute of the McGill University Health Centre

研究点 (4)

Loading locations...

相似试验