NCT07034989CompletedNot Applicable
Investigation of the Effectiveness of Telerehabilitation-Assisted Exercise Training in Individuals With Rheumatoid Arthritis-Associated Interstitial Lung Disease
Zülal TATAR1 site in 1 country10 target enrollmentStarted: March 5, 2025Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 10
- Locations
- 1
- Primary Endpoint
- Oxygen Saturation Measurement
Study Overview
Brief Summary
This study aimed to evaluate the effectiveness of asynchronously implemented telerehabilitation-supported respiratory physiotherapy and function-oriented trunk stabilization exercises, which have not been previously applied in individuals with RA-IAH.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Diagnosed with RA according to the 2010 EULAR/American College of Rheumatology diagnostic criteria
- •Individuals with RA-associated Interstitial Lung Disease
- •Individuals aged ≥18
- •Agreeing to attend regular training throughout the study
- •Having access to the internet and a computer
Exclusion Criteria
- •10 pack-year smoking history
- •Surgery or arthroscopic surgery within the last year
- •Having any neurological or psychological disease that may prevent participation
- •Patient's inability to comply with evaluation and education
- •Having a psychiatric disease that will affect cooperation
- •Individuals with serious functional limitations and cardiopulmonary and/or neurological disease unrelated to RA
Arms & Interventions
Control Group
No Intervention
Asynchronous exercise group
Active Comparator
Intervention: Exercise (Other)
Outcomes
Primary Outcomes
Oxygen Saturation Measurement
Time Frame: Evaluations started immediately after receiving ethics committee approval and will be completed within 3 months, which is the study period.
Secondary Outcomes
- Modified Medical Research Council Dyspnea Scale(Evaluations started immediately after receiving ethics committee approval and will be completed within 3 months, which is the study period.)
- Evaluation of respiratory muscle strength(Evaluations started immediately after receiving ethics committee approval and will be completed within 3 months, which is the study period.)
- Modified Borg Scale(Evaluations started immediately after receiving ethics committee approval and will be completed within 3 months, which is the study period.)
- Visual Analog Scale(Evaluations started immediately after receiving ethics committee approval and will be completed within 3 months, which is the study period.)
- Leicester Cough Survey(Evaluations started immediately after receiving ethics committee approval and will be completed within 3 months, which is the study period.)
- St. George's Respiratory Survey(Evaluations started immediately after receiving ethics committee approval and will be completed within 3 months, which is the study period.)
- Short Form-36 Quality of Life Survey(Evaluations started immediately after receiving ethics committee approval and will be completed within 3 months, which is the study period.)
- Health Assessment Questionnaire(Evaluations started immediately after receiving ethics committee approval and will be completed within 3 months, which is the study period.)
- Disease Activity(Evaluations started immediately after receiving ethics committee approval and will be completed within 3 months, which is the study period.)
Investigators
Zülal TATAR
Researcher
Pamukkale University
Study Sites (1)
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