Effects of Acupuncture on Symptoms of Stable Angina
Recruiting now · Not applicable
Conditions studied: Angina, Stable
In brief
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.
Key facts
- Study ID
- NCT06311461
- Run by
- University of California, Los Angeles
- People needed
- 112
- Starts
- 2024-04-01
- Expected to finish
- 2027-06-30
- Last updated by the study team
- 2025-04-03
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of stable angina or chest pain syndrome for at least 1 month (pain, pressure, or discomfort in the chest or other areas of the upper body)
- Treated with medical therapy for at least 1 month
- Experiencing symptoms at least once per week
- Speak and read English
- 21 years of age minimum
You may not qualify if…
- Pregnancy as some acupuncture points included in the protocol are contraindicated in pregnancy
- Physical or cognitive limitations that will prevent informed consent or completion of study tasks
- Use of steroid or prescription analgesic medications
- Concomitant biofeedback, professional massage and acupuncture.
Where it is running
- UCLA School of Nursing — Los Angeles, California, United States (enrolling)
Full record on ClinicalTrials.gov
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