Exploring Central and Bridge Symptoms in Patients with Lung Cancer: A Network Analysis.
Yuanyuan Luo, Jiahui Luo, Qing Su...
https://pubmed.ncbi.nlm.nih.gov/38704342Actively Recruiting
Led by The University of Hong Kong · Updated on 2026-05-22
80
Participants Needed
2
Research Sites
8 weeks
Total Duration
T
The University of Hong Kong
Lead Sponsor
T
The University of Hong Kong-Shenzhen Hospital
Collaborating Sponsor
Researchers are evaluating the effects of acupressure on cough and related symptoms such as shortness of breath and fatigue in lung cancer survivors. This randomized controlled trial aims to see if acupressure can reduce these symptoms, improve symptom burden, and enhance health-related quality of life and functional ability in patients with lung cancer. The study addresses the significant impact that cough and its related symptoms have on lung cancer survivors' quality of life and overall survival. Participants are randomly assigned to one of two groups: one group receives an 8-week acupressure intervention, while the other receives an educational booklet about lung cancer, cough causes, and management. The acupressure group attends two hospital training sessions in the first week to learn the technique, then performs acupressure daily on 15 specific points twice a day and during coughing episodes as needed. The education group receives the booklet after baseline assessment and will be offered acupressure later after the study ends. Participants keep diaries of their acupressure practice and symptoms and are assessed four times: before starting (baseline), after one week, after eight weeks, and eight weeks after the intervention ends. Researchers measure cough, quality of life related to cough, symptom clusters, fatigue, shortness of breath, symptom burden, functional capacity, and overall health-related quality of life. Follow-up continues for 16 weeks to monitor lasting effects and safety throughout the study period.
CONDITIONS
Acupressure for Cough in Lung Cancer Survivors
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 8 weeks
Participants in the acupressure group will attend two hospital training sessions in the first week to learn correct acupressure techniques. They will then perform acupressure daily for 8 weeks, pressing specific acupoints twice a day and as needed during cough episodes. Trainers will follow up twice weekly by phone or face-to-face to support and assess their practice. Participants in the education group will receive an educational booklet and complete evaluations alongside the acupressure group.
2 training sessions and twice-weekly follow-up contacts during 8 weeks
Duration - 8 weeks
After completing the 8-week intervention, participants are followed for an additional 8 weeks to assess the lasting effects of the intervention on cough and related symptoms.
Visits at 16 weeks after baseline
Total: 2 locations
1
University of Hong Kong-Shenzhen Hospital
Shenzhen, Guangdong, China, 0755
Actively Recruiting
2
Queen Mary Hospital
Hong Kong, Hong Kong, 0000
Not Yet Recruiting
M
Mengyao Cao
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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