Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT05417724 · ClinicalTrials.gov registry record · NA
Utilizing Battlefield Acupuncture(BFA) to Treat Chronic Pain for Homeless and at Risk Veterans.
A NA study, sponsored by Edith Nourse Rogers Memorial Veterans Hospital.
- Completed
- Registry status
- NA
- Development phase
- 34
- Enrollment target
NCT05417724: Completed NA study, sponsored by Edith Nourse Rogers Memorial Veterans Hospital.
NCT05417724 is a NA study that has completed, run by Edith Nourse Rogers Memorial Veterans Hospital. The registered enrollment target is 34 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05417724, a NA study, has completed, sponsored by Edith Nourse Rogers Memorial Veterans Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 34 participants
- Enrollment target
Study 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.
Primary Outcome
Whether 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.
Interventions
- OTHER Battlefield Acupuncture
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 34 participants |
| Start Date | 2022-03-28 |
| Est. Completion | 2023-09-05 |
| Phase | NA |
What the finished NCT05417724 record still lists
NCT05417724 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).
The record links to 0 conditions, and to 1 intervention - of which Battlefield Acupuncture is the first listed.
NCT05417724 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05417724 about?
NCT05417724 is a clinical study titled "Utilizing Battlefield Acupuncture(BFA) to Treat Chronic Pain for Homeless and at Risk Veterans.". 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.
What is the current status of trial NCT05417724?
This trial is currently completed. It is a NA study. The enrollment target is 34 participants. The study started on 2022-03-28. Estimated completion is 2023-09-05.
What interventions are being tested in trial NCT05417724?
The interventions under investigation include: Battlefield Acupuncture (OTHER).
Who is sponsoring clinical trial NCT05417724?
This trial is sponsored by Edith Nourse Rogers Memorial Veterans Hospital, which has 3 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05417724's enrollment target sits among peer trials
34 1570th of 2000 higher than 427 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT02897063 · 34 participants · Phase 1
Effects of Midodrine and Droxidopa on Splanchnic Capacitance in Autonomic Failure
- NCT03906617 · 34 participants · Phase 4
Bupivacaine/Epinephrine +Dexamethasone vs. Liposomal Bupivacaine
- NCT03992378 · 34 participants · NA
Neuromodulation to Regulate Inflammation and Autonomic Imbalance in Sepsis
- NCT04047849 · 34 participants · Phase 4
Latency Antibiotics in Previable PPROM, 18 0/7- 22 6/7 WGA
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI