NCT06128772 Utilizing Battlefield Acupuncture to Treat Chronic Pain
| NCT ID | NCT06128772 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Edith Nourse Rogers Memorial Veterans Hospital |
| Condition | Chronic Pain |
| Study Type | INTERVENTIONAL |
| Enrollment | 125 participants |
| Start Date | 2023-12-30 |
| Primary Completion | 2025-12-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 125 participants in total. It began in 2023-12-30 with a primary completion date of 2025-12-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This research study will evaluate the effectiveness of utilizing Battlefield Acupuncture (BFA) on veterans with with a history of substance use disorder and chronic pain for 8 weeks. Primary Aim: The primary aim of this study is to evaluate the effectiveness of using BFA to treat chronic pain in veterans with a history of substance use disorder. Secondary Aim: This study will also evaluate the impact that BFA treatment for pain may have on subjects' stress, mood and sleep patterns over 8 weeks. In addition, each subject will be complete behavioral research tools to measure: depression, anxiety, and substance use at 3 different points in this study. Hypothesis: The use of BFA on veterans with chronic pain will decrease their pain and substance use and improve their quality of life.
Eligibility Criteria
Inclusion Criteria: Eligibility criteria include: * they are 18 years or older * they have a history of substance use disorder, * history of chronic pain * availability to participate in the study for 16 weeks. Exclusion Criteria: * female veterans who are pregnant. * history of bleeding disorders or currently on older blood thinning medications that cause excessive bleeding. * currently being treated for an active infection of the outer ear (relative contraindication). -- currently have a PICC line in their body or are receiving IV antibiotics. * fear of needles/tacks, and/or * undiagnosed pain complaint
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06128772 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Chronic Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06128772 currently recruiting?
Yes, NCT06128772 is actively recruiting participants. Contact the research team at Cathy.StPierre@va.gov for enrollment information.
Where is the NCT06128772 trial being conducted?
This trial is being conducted at Bedford, United States.
Who is sponsoring the NCT06128772 clinical trial?
NCT06128772 is sponsored by Edith Nourse Rogers Memorial Veterans Hospital. The trial plans to enroll 125 participants.
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