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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05417724
Enrollment
34
Registered
2022-06-14
Start date
2022-03-28
Completion date
2023-09-05
Last updated
2023-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acupuncture, Homelessness, Pain, Veterans

Brief summary

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.

Detailed 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. 4\. Findings: Pending 5\. 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. 6\. Impact/Significance: Pending

Interventions

Battlefield Acupuncture

Sponsors

Edith Nourse Rogers Memorial Veterans Hospital
Lead SponsorFED

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Recruitment of veterans with chronic pain who are interested in being treated with Battlefield Acupuncture (BFA).

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Reduction in pain4 monthsWhether the use of BFA on veterans with chronic pain will decrease pain. Questionnaire. The pain scale is based on 0-10 with a higher score indicating an increase in pain and the lower score indicating a decrease in pain level.

Secondary

MeasureTime frameDescription
Change in pain may impact behavioral health issues.4 monthsWhether effective treatment for chronic pain has an impact on behavioral health issues. Patient Health Questionnaire (PHQ-4) will measure changes in anxiety and depression based on a numerical score from 0-4. This questionnaire is broken down into 4 questions- 2 focused on anxiety and two questions focused on depressions. Each question has a likert scale to select a number from 0-3. The higher the number, the higher the level of anxiety/depression. The cumulative score is based on a score of 0-12, with the higher scores indicating higher psychological distress.
Change in pain may impact housing stability4 monthsWhether effective treatment for chronic pain has an impact on housing stability as measured by the housing stability questionnaire. this questionnaire asks questions about the number of nites in the past 30 days, a research subject has spent in a variety of settings. The scale is 0-30 with the higher the number, the more transient the person's current living situation. The purpose is to see if a change in pain levels will impact the number of nights in transitional housing. The higher the pain level an positively/negatively impact the numbers of nite in transitional housing
Change in pain may impact substance use.4 monthsWhether effective treatment for chronic pain has an impact on substance use as measured by the substance use questionnaire. This questionnaire asked each subject to identify the number of drinks/drugs that the subject has consumed in the past 30 days.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026