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Study identifier: NCT07315672 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Acupressure for Cough in Lung Cancer Survivors

Condition: Lung Cancer (Diagnosis) · Acupressure · Coughing  ·  Sponsor: The University of Hong Kong

PhaseNA
Planned participants80
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this randomized controlled trial is to examine the effect of an acupressure intervention in alleviating cough and reducing co-occurring symptoms (dyspnea, cough, and fatigue) in patients with lung cancer. The hypotheses are: 1. Acupressure can alleviate cough in lung cancer survivors; 2. Acupressure can reduce a cough-related symptom cluster (dyspnea-cough-fatigue) experienced by lung cancer survivors; 3. Acupressure can reduce the symptom burden and improve the health-related quality of life and functional capacity of lung cancer survivors experiencing cough. Participants will: Receive acupressure for 8 weeks or receive an education booklet; Keep a diary of their acupressure practice and symptoms; Be assessed at baseline (T0), early intervention (T1), post-intervention (T2), and 8 weeks after the intervention period (T3).

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

Talk to the study team

Mengyao Cao  ·  +852-96733602  ·  u3590805@connect.hku.hk

Always discuss trial participation with your own doctor first.

Locations (2)

University of Hong Kong-Shenzhen HospitalShenzhen, Guangdong, ChinaRecruiting
Queen Mary HospitalHong Kong, Hong KongNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07315672