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Clinical Trials/NCT05205434
NCT05205434CompletedNot Applicable

Efficacy of Synchronous and Asynchronous Telerehabilitation in COVID-19 Discharges

Bitlis Eren University2 sites in 1 country57 target enrollmentStarted: September 25, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
57
Locations
2
Primary Endpoint
Incremental Shuttle Walk Test (ISWT)

Study Overview

Brief Summary

Investigators aimed to evaluate the effectiveness of exercise programs given by synchronous and asynchronous telerehabilitation methods in patients after discharge from COVID-19.

Detailed Description

Fifty seven participants will be enrolled. Participants will be randomly divided into 3 groups.

For this purpose, patients will be recruited at the time of discharge from the hospital and two experimental groups with the same physical therapy and educational program will be carried out. participants in the control group will only educational program. Participants in experimental groups will be followed using videoconference interviews from synchronous telerehabilitation methods and mobile application from asynchronous telerehabilitation methods at home. These participants will be given an 8-week exercise program. The exercise program will consist of physical exercises (aerobic and strength exercises) along with breathing exercises and the patients will be evaluated before and after the treatment.

After treatment programs, the functional capacity, performance, and hemodynamic parameters of the participants will be evaluated. Quality of life, physical activity level, anxiety-depression, and fatigue severity will also be evaluated with questionnaires.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • COVID-19 patients in the subacute period discharged
  • Be 18 years or older
  • Having received oxygen therapy or mechanical ventilation support in the hospital
  • Access to online interviews and web-based exercises with a secure internet connection
  • Having sufficient speaking and hearing skills for telerehabilitation
  • Volunteer to participate in research

Exclusion Criteria

  • Unstable clinical condition
  • Having had cerebrovascular disease, intra-articular drug injection or surgery of the lower extremities in the last 6 months
  • Inability to walk independently, even with an assistive device
  • Having serious neuromuscular problems
  • Not being cooperative enough to answer and understand questionnaires and scales

Outcomes

Primary Outcomes

Incremental Shuttle Walk Test (ISWT)

Time Frame: Change from baseline walking distance (meters) of the patients at the end of the 8th week and, postintervation sixth months

The participant will be asked to walk around two 9-meter cones and complete them within the given time. Oxygen saturation and heart rate will be measured before and immediately after the test. They will be asked to self-report dyspnea and fatigue according to the modified Borg scale (0-10).

Secondary Outcomes

  • 30-Second Chair Stand Test (30 CST)(Change from baseline number of sitting and staying of the patients at the end of the 8th week and, postintervation sixth months)
  • Brief Physical Performance Battery (BPPB)(Change from baseline score of the patients at the end of the 8th week and, postintervation sixth months)

Investigators

Sponsor
Bitlis Eren University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Abdurrahman Tanhan

Research Assistant

Bitlis Eren University

Study Sites (2)

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