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Study identifier: NCT07195838 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Mindful-Breath for People With COPD

Condition: Mindfulness · Pulmonary Rehabilitation · Chronic Obstructive Pulmonary Disease (COPD)  ·  Sponsor: The University of Hong Kong

PhaseNA
Planned participants60
Who can joinAll sexes, 50 Years to 80 Years
Healthy volunteersNo

About this study

Individuals living with chronic obstructive pulmonary disease (COPD) often suffer from stress and behavioral risks such as physical inactivity. In an attempt to promote healthy behaviors and overall wellbeing among this particular population, this study aims to develop and evaluate a personalized Mindful-Breath intervention combining telehealth technology and mindfulness for COPD patients. This is an assessor-blinded, two-arm exploratory randomized controlled trial with a sequential mixed-method design. A total of 60 participants will be recruited and randomly assigned to either intervention or control group using 1:1 ratio. Intervention group will go through 8 weekly 60-min hybrid group sessions, combining mindfulness-based pulmonary rehabilitation and lifestyle modification. Personalized mindfulness-based lifestyle counselling through instant messages with chat-based support throughout the 8-week intervention period will also be provided. Control group will receive a single in-person 60-min group session on general education on pulmonary rehabilitation and lifestyle modification and will only receive reminder messages for follow-ups. Variables such as time spent on physical activity, lung function, perceived stress, symptom burden and health-related quality of life will be collected at three time-points (T0: baseline, prior to randomization; T1: immediate post-intervention; T2: 3-month post-intervention).

This description comes directly from the study's public registry record.

Talk to the study team

Jojo Yan Yan Kwok  ·  85239176644  ·  jojoyyk@hku.hk

Always discuss trial participation with your own doctor first.

Locations (1)

School of Nursing, The University of Hong Kong, Hong KongHong Kong, Hong KongRecruiting

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Source record: clinicaltrials.gov/study/NCT07195838