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Short Term Results of Tele-Rehabilitation

Short Term Outcomes of Tele-Rehabilitation in Patients With Post-Covid Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05381675
Enrollment
60
Registered
2022-05-19
Start date
2022-05-20
Completion date
2023-08-01
Last updated
2023-08-29

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

Conditions

COVID-19, Dyspnea

Keywords

Tele-rehabilitation, COVID-19

Brief summary

Most people who have coronavirus disease (COVID-19) recover completely without any sequelae. However, some patients continue to experience symptoms of COVID-19 even though their tests turn negative. This clinical spectrum that occurs after acute infection is called the post-COVID syndrome (PCS). Dyspnea, pain, decreased exercise capacity, limitations in activities of daily living, poor sleep quality, anxiety and depression are common symptoms in PCS. The aim of our study is to examine the effect of tele-rehabilitation-based exercise program on dyspnea, pain, functional capacity, sleep quality, anxiety and depression in individuals with PCS.

Interventions

OTHERTele-rehabillitation

Tele-rehabilitation program will be performed by physiotherapist two times a week for six consecutive weeks. Program including the following exercises: Breathing exercises Aerobic exercises Flexibility Strengthening exercises

The prescribed exercise program will be performed two times a week for six consecutive weeks. Program including the following exercises: Breathing exercises Aerobic exercises Flexibility Strengthening exercises

Sponsors

Harran University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Being between the ages of 18-75, * Being in stable medical condition, conscious and cooperative, * Having had COVID and continuing symptoms * Volunteering to participate in the study, * Own a device that can be connected online independently or with support from family members.

Exclusion criteria

SpO2 \< 92%, * Hypotension (Systolic Blood Pressure \< 90 mmHg or Diastolic Blood Pressure \< 60mmHg) * Having chronic respiratory disease (COPD, Asthma, etc.) * Having a stroke or neurodegenerative disease. * Not being willing to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Change from the baseline to the 6th week in mMRC (Modified Medical Research Council) Dyspnoea ScaleBaseline and 6th weekThe mMRC Dyspnoea Scale is used to assess the degree of baseline functional disability due to dyspnoea

Secondary

MeasureTime frameDescription
Change from the baseline to the 6th week in NPRSBaseline and 6th weekThe Numerical Rating Scale (NPRS-11) is an 11-point scale for self-report of pain. It is the most commonly used unidimensional pain scale. The respondent selects a whole number (integers 0-10) that best reflects the intensity (or other quality if requested of his/her pain.
Change from the baseline to the 6th week in the 5 times sit to stand test (5XSST)Baseline and 6th weekThe 5XSST scoring is based on the amount of time (to the nearest decimal in seconds) a patient is able to transfer from a seated to a standing position and back to sitting five times. The equipment need in performing 5XSST test includes: Stopwatch and standard height chair with straight back.
Change from the baseline to the 6th week in the Hospital Anxiety and Depression ScaleBaseline and 6th weekThe Hospital Anxiety and Depression Scale (HADS) was devised to measure anxiety and depression in a general medical population of patients. 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.
Change from the baseline to the 6th week in the The Pittsburgh Sleep Quality IndexBaseline and 6th weekThe Pittsburgh Sleep Quality Index (PSQI) is a measure of self-reported sleep quality and sleep disturbance. Scoring Using a four-point, Likert-type scale, respondents indicate how frequently they exhibit certain sleep behaviors (0 = few, 1 = some- times, 2 = often, and 3 = almost always). The PSQI takes about 10 minutes to complete and it doesn't involve any procedures or interventions.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026