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Utilizing Battlefield Acupuncture(BFA) to Treat Chronic Pain for Homeless and at Risk Veterans.

E

Edith Nourse Rogers Memorial Veterans Hospital

Status

Completed

Conditions

Homelessness
Veterans
Acupuncture
Pain

Treatments

Other: Battlefield Acupuncture

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT05417724
1645513

Details and patient eligibility

About

This research study will evaluate the effectiveness of utilizing Battlefield Acupuncture (BFA) on homeless and at risk for homelessness veterans with chronic pain for 12 weeks.

Full description

Methodology: This is a mixed methods prospective design study. A total of 35 subjects will be recruited for this study. The primary study outcome variables are: pain level- pre and post treatment, stress, mood and usual activity levels, sleep patterns and behavioral factors such as ; anxiety, depression, suicidal ideation, substance use and housing stability.

  1. Findings: Pending

  2. Clinical Relationships: This study is conducted to demonstrate whether or not BFA treatment will decrease pain and improve quality of life for homeless and at risk for homelessness veterans.

  3. Impact/Significance: Pending

Enrollment

34 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Eligibility criteria include:

  • they are 18 years or older
  • they are homeless or at risk for homelessness veterans who are enrolled in the VA Bedford Healthcare system and registered in one of the HUD-VASH or HCHV programs,
  • history of chronic pain.
  • Availability to participate in the study for 4 months.

If they meet these criteria, they will be asked to complete the Informed consent to enroll in the study.

Exclusion criteria

  • female veterans who are pregnant
  • history of bleeding disorders or currently on blood thinning medications
  • currently being treated for an active infection of the outer ear.
  • currently have a PICC line in their body or are receiving IV antibiotics.
  • fear of needles/tacks
  • undiagnosed pain complaint

Our recruitment plan invites all eligible veterans and is just, fair, and equitable.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

34 participants in 1 patient group

Battlefield Acupuncture
Other group
Description:
All subjects will receive BFA treatment weekly for 12 weeks.
Treatment:
Other: Battlefield Acupuncture

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Cathy M St Pierre, PhD; Alexandra Howard, BS

Data sourced from clinicaltrials.gov

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