The Effectiveness of Qigong in Managing a Cluster of Symptoms (Breathlessness-Fatigue-Anxiety) in Patients with Lung Cancer: A Randomized Controlled Trial.
Alex Molassiotis, Dau Van Vu, Shirley Siu Yin Ching
https://pubmed.ncbi.nlm.nih.gov/33847150/Actively Recruiting
Led by The University of Hong Kong · Updated on 2026-08-11
80
Participants Needed
2
Research Sites
8 weeks
Total Duration
Researchers are evaluating the effects of a self-administered acupressure intervention on cough and related symptoms in lung cancer survivors. The study aims to see if acupressure can reduce cough, lessen a symptom group involving dyspnea, cough, and fatigue, and improve overall symptom burden, functional capacity, and quality of life for these patients. This is a randomized controlled trial focusing on supportive care for lung cancer survivors. Participants are randomly assigned to either an 8-week acupressure program or an education group. Those in the acupressure group attend two training sessions at the hospital during the first week to learn proper techniques. They then perform acupressure daily on 15 specific points at least twice a day and during coughing episodes. The education group receives a booklet about lung cancer, cough causes, and management strategies. Trainers follow up with acupressure participants twice weekly to support and assess their practice. Participants will keep diaries recording their acupressure practice and symptoms. They are assessed at four times before treatment, after 1 week, after 8 weeks, and 8 weeks post-intervention. Researchers evaluate cough severity, cough-related quality of life, the dyspnea-cough-fatigue symptom cluster, fatigue, symptom burden, functional capacity, and health-related quality of life. The study runs from baseline through an 8-week intervention and an 8-week follow-up period, with ongoing monitoring via diaries and trainer contacts.
CONDITIONS
Acupressure for Cough in Lung Cancer Survivors
M
Mengyao Cao
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The University of Hong Kong
Lead Sponsor
The University of Hong Kong-Shenzhen Hospital
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 8 weeks
Participants either receive training and perform acupressure daily for 8 weeks or receive an educational booklet with information on lung cancer and cough management.
Two hospital training sessions for acupressure group; regular follow-up twice weekly
Duration - 8 weeks
Participants are assessed 8 weeks after the intervention to monitor cough, symptoms, and quality of life.
Assessments at 8 weeks post-intervention
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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https://pubmed.ncbi.nlm.nih.gov/37948789/The University of Hong Kong
Lead Sponsor
The University of Hong Kong-Shenzhen Hospital
Collaborating Sponsor