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Recruiting Not applicable

Telerehabilitation in Patients With Idiopathic Pulmonary Fibrosis

NCT05190211 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2021-11-26
Last updated
2025-11-21

Condition(s) studied

IPF

Investigational drug(s) / intervention(s)

Telerehabilitation exercise programVideobased exercise program

Telerehabilitation exercise program: TGr will be given online exercises, synchronized 2 days a week, and a home program for 1 day, accompanied by a physiotherapist, via videoconference on the group smartphone.

Videobased exercise program: After 1 session of online simultaneous exercise training in the company of a physiotherapist via videoconference on the smart phone, an exercise video including the exercises will be sent to them and the patients will be asked to do their exercises 3 days a week. The subjects will be asked to keep an exercise diary and the status of the diaries will be followed by calling them once a week.

Study summary

It is to determine the effectiveness of different telerehabilitation exercise programs received to 2 groups randomly formed in idiopathic pulmonary fibrosis (IPF) patients. The cases meeting the inclusion criteria will be randomized and divided into two groups, the groups will be named as Telerehabilitation Exercise Group (TGr) and Video Group (VGr).

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Being between the ages of 18-75 * Having a diagnosis of IPF disease diagnosed according to the following clinical diagnostic criteria according to the American Thoracic and European Respiratory Societies (ATS-ERS) * Presence of dyspnea on exertion * Stable clinical state at the time of admission without infection or exacerbation in the previous 4 weeks Exclusion Criteria: * Patients with severe comorbid diseases, unstable coronary artery disease, collagen vascular diseases and needing high flow oxygen therapy (˃ 3-4 L \\min). * A history of effort-related syncope or any comorbidity (such as severe orthopedic or neurological deficits or unstable heart disease) that precludes exercise training. * Participation in a pulmonary rehabilitation program within the past 12 months.

Primary outcome measure(s)

  • The exercise capacity — Change from baseline 6 minute walking distance at 8 weeks
    The exercise capacity will be assessed by the 6 minute walking test.The test was conducted in a 30-meter corridor in line with American Thoracic Society (ATS) guidelines.

Trial sites (1)

FacilityCityRegionStatus
Yedikule Chest Disease Hospital Istanbul Zeytinburnu Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05190211 on ClinicalTrials.gov ↗ ← All trials in Turkey