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Telerehabilitation After Coronavirus

Telerehabilitation After Covid-19: Effectiveness of Respiratory and Aerobic Training

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04473898
Enrollment
35
Registered
2020-07-16
Start date
2020-06-19
Completion date
2021-02-17
Last updated
2021-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID

Keywords

Covid-19, Telerehabilitation, Respiratory Exercises, Aerobic Exercises

Brief summary

The aim of the study is to investigate the effects of telerehabilitation program on COVID-19 symptoms, quality of life, level of depression, perception of dyspnea, sleep, fatigue, kinesiophobia and patient satisfaction in individuals diagnosed with COVID-19.

Detailed description

Because of the risk of infection, telerehabilitation applications are recommended for patients with COVID-19. There are no studies in the literature evaluating the effectiveness of telerehabilitation program after COVID-19. In particular, the importance of the first eight weeks after the disease was emphasized. It is thought that the telerehabilitation program will improve the functional capacities and quality of life of patients in order to adapt to the daily life after the infection more easily, to cope with the symptoms brought about by the disease more easily and to prevent the respiratory distress, intensive care stay and inactivity due to muscle weakness.

Interventions

OTHERAerobic Exercise Training

Aerobic exercises using all body muscles and that one can do on their own after being shown online

BEHAVIORALPatient Education

Patient education about covid-19 and hygiene education

OTHERRespiratory Exercise Training

Respiratory exercises that one can do on their own after being shown online

Sponsors

KTO Karatay University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Intervention model description

It is planned to include 3 groups in the study. The group 1 will be informed about covid-19 and hygiene. Aerobic exercise will be offered to Group 2, aerobic exercise + breathing exercises will be offered to Group 3. The persons to be included in the groups will be determined randomly.

Eligibility

Sex/Gender
ALL
Age
25 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* volunteering to participate in the study * at least once diagnosed with COVID-19, * has a cognitive level that can adapt to online exercises, * having a physical condition suitable for exercises * staying in hospital due to covid-19

Exclusion criteria

* refuse to participate in the study * having neurological, cardiac, respiratory disease that prevents exercise

Design outcomes

Primary

MeasureTime frameDescription
DyspnoeabaselineIt will be evaluated by the Modified Medical Research Council (mMRC). It consists of 5 items between 0 and 4. The increase in the score indicates the severity of dyspnea.
Anxiety and DepressionbaselineIt will be evaluated by the Hospital Anxiety and Depression Scale (HADS). The questionnaire comprises seven questions for anxiety and seven questions for depression, and takes 2-5min to complete. Although the anxiety and depression questions are interspersed within the questionnaire, it is vital that these are scored separately. Cut-off scores are available for quantification, for example a score of 8 or more for anxiety. The increase in the score indicates the severity of anxiety and depression.
Sleep QualitybaselineIt will be evaluated by pittsburgh sleep quality index
Health Related Quality of LifebaselineIt will be evaluated by SF-36

Secondary

MeasureTime frameDescription
Patient Satisfaction6 weeks laterIt will be evaluated by patient satisfaction scale. Likert scale questionnaire proposed seven dimensions of patient satisfaction directed toward their doctors. These are general satisfaction, technical quality, interpersonal manner, communication, financial aspects, time spent with doctor, and accessibility and convenience. Increased score indicates decreased satisfaction. The minimum score is 18, the maximum score is 90.
FatiguebaselineIt will be evaluated by Fatigue Severity Scale. A self-report scale of nine items about fatigue, its severity and how it affects certain activities. Answers are scored on a seven point scale where 1 = strongly disagree and 7 = strongly agree. This means the minimum score possible is nine and the highest is 63.
KinesiophobiabaselineIt will be evaluated by Kinesiophobia Causes Scale. The questionnaire consist of 20 closed questions, assessed in a range from 0 to 100 - a higher score indicating a higher fear of movement

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026