Ignite Creation Date:
2024-07-17 @ 11:25 AM
Last Modification Date:
2024-10-26 @ 3:34 PM
Study NCT ID:
NCT06497582
Status:
RECRUITING
Last Update Posted:
2024-07-12
First Post:
2024-05-28
Brief Title:
Self-acupressure and Zhan Zhuang for Symptom Cluster Management
Sponsor:
The Hong Kong Polytechnic University
Organization:
The Hong Kong Polytechnic University
Study Overview
Official Title:
Self-acupressure and Zhan Zhuang for Pain Fatigue and Sleep Disturbance in Breast Cancer Survivors A Pilot Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
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 111 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
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None