Self-acupressure and Zhan Zhuang for Symptom Cluster Management

The Hong Kong Polytechnic University

Status: Enrolling

Conditions: Breast Cancer Female; Survivorship

Treatments: Other: self-acupressure; Other: zhan-zhuang

Study type: Interventional

Funder types: Other

Identifiers

NCT06497582

04

Details and patient eligibility

About

The proposed study will be a 3-arm, parallel-group randomized controlled trial on the effects of self-acupressure and Zhan-Zhuang for alleviating pain, fatigue, and sleep disturbance in breast cancer survivors. Subjects will include 54 breast cancer survivors who have experienced a moderate level of pain, fatigue and sleep disturbance. All eligible subjects will be randomized into one of the three groups in a 1:1:1 ratio: Zhan Zhuang group, or self-acupressure group, or wait list control group. Subjects in the Zhan-Zhuang group will receive up to 8 weeks of the intervention consisting of a training course over two weeks followed by self-practice for 6 weeks. Those in the self-acupressure group will attend an acupressure training course for two weeks and then, will be asked to practice self-acupressure for 6 weeks. The wait list control group will be provided with delayed self-acupressure or Zhan Zhuang at the end of the study. Outcome assessment will be conducted at baseline, week 8 (post-intervention) and week 12 (4 week follow-up). Primary outcomes include pain, fatigue and sleep disturbance. Secondary outcomes include psychological distress and health-related quality of life. Qualitative data will be collected from selected participants who have received the intervention.

Enrollment: 54 estimated patients

Sex: Female

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• a female adult aged 18 and older;
• a diagnosis of early-stage (Stage I, II, or III) breast cancer;
• completion of surgery, and/or chemotherapy and/or radiotherapy;
• have at least a moderate level of pain, fatigue and sleep disturbance as measured on 0-10 numerical rating scales, with a score of ≥ 3 for each symptom during the past one month;
• willing to use WhatsApp messenger for follow-ups;
• being able to communicate in Chinese

Exclusion criteria

• prior use of acupuncture, acupressure, Zhan Zhuang, or other types of Zhan Zhuang within the past three months;
• currently receiving progressive muscle relaxation, mindfulness-based stress reduction, and other body mind exercise (e.g. yoga) for the treatment of pain, fatigue, and sleep disturbance;
• mentally incapable of participating in the study as indicated by the Hong Kong version of Montreal Cognitive Assessment score;
• inability to perform self-care as indicated by the Karnofsky Performance Scale score<70

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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54 participants in 3 patient groups

Zhan-zhuang group

Experimental group

Description:

The intervention will last 8 weeks and comprise the following 1) Two sessions of Zhan Zhuang training(2 hours per session/week, totally 4 hours) for 2 weeks. (2) self-practice of zhan-zhuang for 6 weeks (daily, at least 20 mins) at home after passing the evaluation by a Zhan-Zhuang master

Treatment:

Other: zhan-zhuang

Self-acupressure group

Experimental group

Description:

The intervention will last 8 weeks and comprise the following 1) Two sessions of self-acupressure training (2 hours per session/week, totally 4 hours) for 2 weeks. (2) self-practice of acupressure for 6 weeks (daily, around 20 mins) at home after passing the evaluation by a licensed traditional Chinese medicine doctor.

Treatment:

Other: self-acupressure

Waitlist control group

No Intervention group

Description:

Usual care only