Acupuncture for reducing pain in stable angina
Effects of Acupuncture on Symptoms of Stable Angina: A Randomized Controlled Trial
This study is testing if a specific acupuncture treatment can help people with stable angina feel less pain compared to those who just watch talks for five weeks.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 112 (estimated) |
| Ages | 21 Years and up |
| Sex | All |
| Sponsor | University of California, Los Angeles Academic / other |
| Locations | 1 site (Los Angeles, California) |
| Trial ID | NCT06311461 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of a standardized 12-point acupuncture protocol in alleviating pain for individuals suffering from stable angina. Participants will be randomly assigned to receive either acupuncture treatments or engage in attention control activities, such as watching non-pain related talks, over a period of five weeks. The study will assess various pain metrics and health-related quality of life measures to determine the impact of acupuncture on angina symptoms and overall patient outcomes. The long-term goal is to improve symptom management for diverse populations affected by angina, particularly those facing social disadvantages.
Who should consider this trial
Good fit: Ideal candidates include adults aged 21 and older with a diagnosis of stable angina or chest pain syndrome who have been on medical therapy for at least one month and experience symptoms weekly.
Not a fit: Patients who are pregnant, have cognitive or physical limitations, or are using certain medications like steroids or analgesics may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a non-pharmacological option for managing pain in patients with stable angina.
How similar studies have performed: Other studies have shown promising results for acupuncture in managing chronic pain conditions, suggesting potential for success in this approach for stable angina.
Eligibility criteria
Show full inclusion / exclusion criteria
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.
Where this trial is running
Los Angeles, California
- UCLA School of Nursing — Los Angeles, California, United States (Recruiting)
Study contacts
- Principal investigator: Holli A. DeVon, PhD — University of California, Los Angeles
- Study coordinator: Holli A. DeVon, PhD
- Email: hdevon@sonnet.ucla.edu
- Phone: 3109107283
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.