NCT06684132Not yet recruiting
Respiratory Muscle Training in Scleroderma
Effects of Respiratory Muscle Training in Patients With Scleroderma With Pulmonary Involvement
Source: ClinicalTrials.gov · Last updated 12 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The aim of this study is to investigate the effects of IMT on respiratory muscle strength, pulmonary function tests, quality of life aerobic capacity, dyspnea, fatigue and physical activity level in scleroderma patients with ILD. The study will include 30 Scleroderma + ILD patients who are under follow-up in Fırat University Rheumatology Department. Patients will be randomly divided into two groups. High intensity intermittent inspiratory muscle training (H-IMT) will be applied to the respiratory muscle training group in addition to the exercise program. Respiratory muscle strength will be assessed by maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP); aerobic capacity will be assessed by exercise test and VO2max. Dyspnea will be assessed with the Modified Medical Research Council Scale; fatigue with the Fatigue Severity Scale; quality of life with the Scleroderma Health Assessment Questionnaire; physical activity level with the International Physical Activity Scale - Short Form
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- First submitted
- 8 Nov 2024
- Start date
- 10 Nov 2024
- Primary completion date
- 10 Jan 2025
- Lead sponsor
- Firat University
- Diseases
- Systemic sclerosis (scleroderma)
- NCT number
- NCT06684132
What you commit to
- Study type: Interventional
- Planned participants: 30
- From 10 Nov 2024 to the primary completion date, 10 Jan 2025
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study design.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients with other concomitant systemic inflammatory rheumatic diseases
Other illness
- Patients with a diagnosis of malignancy
Other
- Patients who are pregnant
- Patients with neurological, orthopedic or congenital problems that prevent physical activity
Who the study is looking for
- 18-65 years old
- Patients whose medical treatment has not changed in the last three months
- Patients who volunteered to participate in the study and were cooperative
- Literate patients
- Patients followed with a diagnosis of SSc
Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.