研究目的
To determine the specific efficacy of 10.6 mm infrared laser moxibustion on cancer-related fatigue (CRF) in breast cancer survivors (BCS) and to evaluate its effect on co-existing symptoms.
研究成果
The trial aims to establish the efficacy of infrared laser moxibustion for CRF and co-morbid symptoms in breast cancer survivors, potentially improving symptom control and quality of life.
研究不足
Partial double-blind trial due to inclusion of a waitlist control group. Conducted in China, limiting generalizability to other populations.
1:Experimental Design and Method Selection:
A randomized, sham-controlled, three-arm trial comparing infrared laser moxibustion (ILM), sham ILM (SILM), and waitlist control (WLC).
2:Sample Selection and Data Sources:
Female breast cancer survivors (stage I–III), aged 18 years and older, at least 12 weeks post primary treatment, with moderate to severe fatigue.
3:List of Experimental Equipment and Materials:
SX10-C1 laser moxibustion devices for ILM and SILM groups.
4:Experimental Procedures and Operational Workflow:
Participants receive 20-minute treatments twice per week for six weeks on four acupoints.
5:Data Analysis Methods:
Mixed effects models to analyze changes in fatigue scores and other outcomes.
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