Telerehabilitation in Patients With Idiopathic Pulmonary Fibrosis
The Effectiveness of Synchronized Online and Video-based Exercise Programs in Patients With Idiopathic Pulmonary Fibrosis
1 other identifier
interventional
44
1 country
1
Brief 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).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2021
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 26, 2021
CompletedStudy Start
First participant enrolled
November 26, 2021
CompletedFirst Posted
Study publicly available on registry
January 13, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
November 21, 2025
April 1, 2025
4.7 years
November 26, 2021
November 20, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The exercise capacity
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.
Change from baseline 6 minute walking distance at 8 weeks
Secondary Outcomes (9)
Forced vital capacity (FVC)
Change from baseline FVC at 8 weeks
Perception of dyspnea
Change from baseline dyspnea perception at 8 weeks
Respiratory muscle strength
Change from baseline respiratory muscle strength at 8 weeks
Peripheral muscle strength
Change from baseline peripheral muscle strength at 8 weeks
Perception of general fatigue
Change from baseline perception of general fatigue at 8 weeks
- +4 more secondary outcomes
Study Arms (2)
Telerehabilitation Group (TG)
EXPERIMENTALVideo Group (VGr)
EXPERIMENTALInterventions
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.
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Yedikule Chest Disease Hospital
Istanbul, Zeytinburnu, 34200, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
November 26, 2021
First Posted
January 13, 2022
Study Start
November 26, 2021
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Last Updated
November 21, 2025
Record last verified: 2025-04