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Sponsor: The University of Hong Kong
Conditions: Lung Cancer (Diagnosis), Acupressure, Coughing, Symptom Cluster
Interventions: acupressure, Education
Countries: China, Hong Kong
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).
Sex: ALL
Age: 18 Years to —
Healthy volunteers: No
Study type: INTERVENTIONAL
Inclusion Criteria: * be at least 18 years of age; * have a diagnosis of LC at any stage and of any pathological type; * have a cough symptom rating ≥3 on a 0 to 10 numeric rating scale within 7 days preceding enrollment; * can perform acupressure independently in daily activities; * be able to read Chinese and communicate in Cantonese or Mandarin; * be able to provide informed consent. Exclusion Criteria: * have unstable chronic diseases other than LC; * have received acupressure or acupuncture within the three months preceding study enrollment; * have serious illnesses or other conditions that prevent the participants from following the intervention protocols; * have a life expectancy of less than 3 months; * Be currently participating in other research programs that may affect the outcomes under investigation.
- Shenzhen, Guangdong, China
- Hong Kong, Hong Kong