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Effects of Acupuncture on Symptoms of Stable Angina

Effects of Acupuncture on Symptoms of Stable Angina: A Randomized Controlled Trial

Who can join

Ages 21 and older · All sexes

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.

About the study

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.

What is being tested

• Acupuncture (procedure)
• Attention control (other)

Sponsor: University of California, Los Angeles · Participants: 112 · Started: Apr 1, 2024

Contact the study team

• Holli A. DeVon, PhD · Phone: 3109107283
• Peter Cabezas · Phone: 310-922-5835

Official record on ClinicalTrials.gov — NCT06311461

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Oct 1, 2026. Each study sets its own eligibility; the study team decides who can join.