Condition: Angina, Stable · Sponsor: University of California, Los Angeles
The goal of this clinical trial is to determine if a standardized 12-point acupuncture protocol will reduce pain in participants with stable angina. This study addresses the critical need to reduce persistent pain for angina. The investigators long-term goal is symptom management for diverse women and men with angina, targeting additional angina burden borne of social disadvantage Participants will be randomized to a 10-acupuncture session protocol, two treatments per week for five weeks, or an attention control group. Participants will view designated, non-pain related Technology, Entertainment, Design Talks equal to the time spent receiving acupuncture (\~7.5-10 hrs.). The investigators will test the efficacy of acupuncture for stable angina/chest pain syndrome to reduce pain and symptoms, improve health-related quality of life, reduce healthcare utilization and and improve patient related health outcomes.
This description comes directly from the study's public registry record.
Holli A. DeVon, PhD · 3109107283 · hdevon@sonnet.ucla.edu
Peter Cabezas · 310-922-5835 · pcabezas@sonnet.ucla.edu
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| UCLA School of Nursing | Los Angeles, California, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06311461