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Short Term Results of Tele-Rehabilitation

H

Harran University

Status

Completed

Conditions

COVID-19
Dyspnea

Treatments

Other: Tele-rehabillitation
Other: Prescribed Exercise Program

Study type

Interventional

Funder types

Other

Identifiers

NCT05381675
İntervention

Details and patient eligibility

About

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.

Enrollment

60 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

60 participants in 2 patient groups

Intervention
Experimental group
Description:
Participants will receive a supervised tele-rehabilitation program 2 days a week for 6 weeks.
Treatment:
Other: Tele-rehabillitation
Control
Other group
Description:
Participants will receive the same rehabilitation program as prescribed.
Treatment:
Other: Prescribed Exercise Program

Trial contacts and locations

1

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Central trial contact

Rüstem Mustafaoğlu

Data sourced from clinicaltrials.gov

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