CI

At a glance

ClinicalIndex Comparison Record
N/AUnknown· 30 target
Drug / intervention
Pulmonary Rehabilitation +1 moreother
Likely dose
Not stated in record
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Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04561479
NCT04561479N/AUnknown

Evaluation of the Effects of Pulmonary Rehabilitation in Patients With Chronic Fibrotic Hypersensitivity Pneumonitis

Gazi University·interventional·Posted Sep 23, 2020·Updated Sep 23, 2020

In Brief

A clinical study evaluating Pulmonary Rehabilitation and Alternative Exercises for Hypersensitivity Pneumonitis and Extrinsic Allergic Alveolitis. Targeting 30 participants.

Detailed Summary

The aim is to evaluate exercise capacity, respiratory functions, respiratory and peripheral muscle strength, inspiratory muscle endurance, physical activity level, quality of life, fatigue, dyspnea, anxiety, depression and investigate the impact of 24-session pulmonary rehabilitation training on these parameters in patients with chronic fibrotic hypersensitivity pneumonitis.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

N/AUnknownOverdue
202120222023202420252026
First PostedSep 23, 2020
Enrollment StartJun 1, 2021
Primary CompletionFeb 1, 2022
Study CompletionJun 1, 2023
TodayJul 1, 2026
Enrollment to primary: 8 monthsPosted 5.8 years ago

Interventions

Pulmonary Rehabilitationother

All exercise program will be applied during supervised session by a physiotherapist. Range of maximal heart rate will be screened by heart rate monitor during supervised session. Training group will receive upper extremity aerobic exercise training using arm ergometer at 60-80% of maximal heart rate (dyspnea perception at 3-4 level as well as fatigue perception at 5-6 level according to Modified Borg Scale). Inspiratory muscle training (Powerbreathe® Wellness-Inspiratory Muscle Trainer) at 50-60% of maximal inspiratory pressure (MIP) and progressive resistance training at 30-60% of 1 RM (using proprioceptive neuromuscular facilitation techniques (flexion, abduction, external rotation/extension, adduction, internal rotation) for upper extremity resistance training; using sandback for knee extensors) will be performed during 24 sessions (3 day/week; 8 weeks)

Alternative Exercisesother

Control group will receive alternative upper extremity exercises combined with breathing exercises. Control group will perform alternative upper extremity exercises combined with breathing exercises during 3 days/week, for 8 weeks