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A Controlled Breathing Intervention to Reduce Stress and Improve Symptoms in COPD Patients (REST) — REST  

COPD Clinical Trial

Official title:
A Controlled Breathing Intervention to Reduce Stress and Improve Symptoms in COPD Patients (REST): A Randomized Pilot Trial

Clinical Trial Summary

This is a parallel design, randomized, controlled pilot trial comparing a controlled breath intervention (REST) to usual care for reducing stress in individuals with COPD.

Clinical Trial Description

This is a parallel design, randomized, controlled pilot trial comparing a controlled breath intervention (REST) to usual care for reducing stress in individuals with chronic obstructive pulmonary disease (COPD). The intervention is based on the breathing techniques of Pranayama. It was developed with patient and stakeholder input and is targeted for individuals with COPD who have moderate levels of stress and symptom burden. The intervention is a 15-minute breathing protocol which will be taught to participants and subsequently evaluated in a clinic setting with surveys, lung function, and cardiac assessments. This intervention will be pre-tested in 6 individuals, revised, and piloted in 30 individuals (15 in intervention group, 15 in control group). This study will answer the question of 1) whether a controlled breath protocol is feasible, acceptable, and safe for patients with COPD and 2) whether any modifications to the intervention are needed for a future multicenter trial to be proposed and conducted after the completion of the pilot trial. We will also 3) obtain sufficient estimates of variability in stress measures to inform statistical planning of a future trial. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06404008
Study type Interventional
Source University of Texas at Austin
Contact Kristina Kashyap, DO
Phone (512) 270-0614
Email kristina.kashyap@austin.utexas.edu
Status Not yet recruiting
Phase N/A
Start date May 2024
Completion date May 2025
View Details
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