Telerehabilitation in COVID-19 Survivors

NCT ID: NCT05074979

Last Updated: 2024-09-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-10-27
• Study Completion Date: 2022-08-30

Brief Summary

This study was carried out in the post-acute period of the telerehabilitation program in individuals with dyspnea who had COVID-19; It will be done to examine the effects on dyspnea, exercise capacity, respiratory functions, activities of daily living, muscle strength, muscle oxygenation, fatigue and quality of life parameters.

Conditions

COVID-19; Telerehabilitation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: DOUBLE

Study Groups

control group

While other groups continue their exercise program for 6 weeks, this group will only be informed after COVID 19.

Group Type: OTHER

informed program

Intervention Type: OTHER

will informed after COVID 19

home exercise program group

this group will implement COVID 19 home exercise program.

Group Type: EXPERIMENTAL

home exercise program

Intervention Type: OTHER

While telerehabilitation sessions will be applied to the participants in the telerehabilitation group for 6 weeks, home exercise program will be given to the home exercise program group and will be applied for 6 weeks.

telerehabilitation group

this group will implement COVID 19 telerehabilitation program.

Group Type: EXPERIMENTAL

telerehabilitation

Intervention Type: OTHER

While telerehabilitation sessions will be applied to the participants in the telerehabilitation group for 6 weeks, home exercise program will be given to the home exercise program group and will be applied for 6 weeks.

Interventions

telerehabilitation

While telerehabilitation sessions will be applied to the participants in the telerehabilitation group for 6 weeks, home exercise program will be given to the home exercise program group and will be applied for 6 weeks.

Intervention Type: OTHER

home exercise program

While telerehabilitation sessions will be applied to the participants in the telerehabilitation group for 6 weeks, home exercise program will be given to the home exercise program group and will be applied for 6 weeks.

Intervention Type: OTHER

informed program

will informed after COVID 19

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Diagnosed with COVID-19 by Computed Tomography (CT) or PCR test between the ages of 18-75,
• Do not have any orthopedic or neurological disease that will affect exercise capacity,
• Individuals who can take and execute verbal orders,
• Have had COVID-19 and at least 2 weeks have passed since the completion of the treatment,
• Individuals who have a computer or smart phone with a camera and internet connection and have the ability to use it (the participant himself or one of his family members living in the same house),
• Individuals who are sedentary (those whose physical activity level is inactive according to the Turkish version of the International Physical Activity Questionnaire (UFAA)),
• Having dyspnea at level 2 or 3 on the Medical Research Council Dyspnea Scale.

Exclusion Criteria

• Those who have not had COVID-19 or acute period patients who are experiencing COVID-19,
• Individuals who cannot be contacted,
• Individuals with chronic heart disease,
• Those with concomitant uncontrolled disease; uncontrolled hypertension (resting blood pressure ≥160 /100mmHg), uncontrolled diabetes (random instantaneous blood glucose>16.7 mmol/l, HbA1C>7.0%),
• Those with concomitant severe organic disease (unstable hemodynamic heart disease, heart failure causing movement limitation, unstable angina, MI or other cardiac disease in the last 12 years),
• Individuals with cerebrovascular disease in the last 6 months,
• Those with digestive system ulcer, thyroid dysfunction or active stage of tuberculosis,
• Patients with Chronic Kidney Failure stage 3 and above according to Glomerular Filtration Rate (GFR),
• Individuals who have undergone intraraticular medication or surgery from their lower extremities in the last 6 months,
• Individuals who cannot walk independently,
• Individuals with any mental illness that may prevent them from living independently or receiving treatment,
• Uncooperative individuals for assessment and rehabilitation programs,
• Those with alcohol or substance addiction,
• Those who are pregnant, suspected of pregnancy or considering becoming pregnant,
• Participants in another study within the last 3 months or currently.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Bandırma Onyedi Eylül University

OTHER

Sponsor Role: lead

Responsible Party

Canan Demir

Research Assistant

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Bandırma Onyedi Eylül University, Faculty of Health Sciences, Physiotherapy and Rehabilitation Department

Balıkesir, Bandırma, Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

CDemir

Identifier Type: -

Identifier Source: org_study_id