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NCT06311461Recruiting

Effects of Acupuncture on Symptoms of Stable Angina

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

Source: ClinicalTrials.gov · Last updated 3 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
112 (estimated)
First submitted
21 Feb 2024
Start date
1 Apr 2024
Primary completion date
31 Dec 2026
Lead sponsor
University of California, Los Angeles
NCT number
NCT06311461

What you commit to

  • Study type: Interventional
  • Planned participants: 112
  • From 1 Apr 2024 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of steroid or prescription analgesic medications
  • Concomitant biofeedback, professional massage and acupuncture.

Other

  • 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

Who the study is looking for

  • 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

Age in the registry: 21 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UCLA School of Nursing
Coordinator of this site? Confirm its status
Los AngelesUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.