Effects of Acupuncture on Symptoms of Stable Angina
About
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.
Eligibility
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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.
Join this Trial
- Holli Devon
- UCLA Westwood