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NCT03525275
Effect of Battlefield Acupuncture and Physical Therapy Versus Physical Therapy Alone After Shoulder Surgery
NA trial testing Battlefield Acupuncture in Opioid Use in 40 participants. Completed in 15 April 2019.
15 April 2019
Quick facts
| Lead sponsor | Keller Army Community Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 40 |
| Start date | 15 August 2018 |
| Primary completion | 15 April 2019 |
| Estimated completion | 15 April 2019 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Battlefield Acupuncture
- Post-surgical shoulder protocol
Conditions studied
- Opioid Use — all drugs for Opioid Use →
- Pain, Postoperative — all drugs for Pain, Postoperative →
- SLAP Lesion — all drugs for SLAP Lesion →
- Bankart Lesion — all drugs for Bankart Lesion →
Sponsor
Keller Army Community Hospital
Who can join
Adults 17 to 55, any sex, with Opioid Use or Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this randomized clinical trial is to determine the effectiveness of Battlefield Acupuncture (BFA) in addition to usual post-surgical shoulder physical therapy compared to a standard shoulder rehabilitation program in reducing medication use and pain in patients who have undergone shoulder surgery. Measurements of medication (opioid, NSAID, acetaminophen, etc.) use (daily number of pills consumed), pain rating, patient specific functional scale and global rating of change will be taken at 24, 72 hours, 7 days, 14 days and at six weeks post-surgery. It is hypothesized that the inclusion of Battlefield Acupuncture will result in a decrease in medication use and post-surgical pain when compared to rehabilitation alone. The population for this study is male and female DoD beneficiaries, ages 17-55 (17 if cadet) that are not participating in other shoulder research studies. The subjects in the experimental group will receive Battlefield Acupuncture in addition to their respective post-surgical shoulder rehabilitation protocol.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Battlefield Acupuncture and Physical Therapy Versus Physical Therapy Alone After Shoulder Surgery.
Collinsworth KM, Goss DL. · · 2019 · cited 19× · PMID 31456869 · DOI 10.1089/acu.2019.1372
Verify or expand the search:
- PubMed search for NCT03525275
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Battlefield Acupuncture
Trials testing the same drug.
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- NCT07528300 — Effect of Battlefield Acupuncture on Pain Control During Inpatient Treatment of Exertional Rhabdomyolysis · NA · recruiting
- NCT05417724 — Utilizing Battlefield Acupuncture(BFA) to Treat Chronic Pain for Homeless and at Risk Veterans. · NA · completed
- NCT04236908 — Accessible Acupuncture for the Warrior With Acute Low Back Pain · NA · completed
- NCT04218422 — Battlefield Acupuncture for Pain in Hidradenitis Suppurativa · NA · recruiting
Other recruiting trials for Opioid Use
Currently open trials in the same condition.
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- NCT07004686 — Effect of MGRNOX-Guided General Anesthesia on Opioid Consumption in Patients · NA · recruiting
- NCT06981195 — Effects of Lemborexant on Insomnia and Its Relationship to Mood and Behavior on Opioid Use Disorder Subjects · Phase 2 · recruiting
- NCT06806163 — Machine-Learning Prediction and Reducing Overdoses With EHR Nudges · NA · recruiting
- NCT06909851 — Comparison of Pain Relief After Arthroscopic Knee Surgery: Adductor Canal Block and Genicular Nerve Block · NA · recruiting
Other Keller Army Community Hospital trials
Trials by the same sponsor.
- NCT06988709 — Examining the Most Effective Method to Reduce Running Ground Contact Time · NA · recruiting
- NCT05453110 — Does Self-efficacy Predict Outcomes Among U.S. Military Academy Cadets During Initial Entry Training? · NA · completed
- NCT05506072 — Blood Flow Restriction Training Versus Standard Physical Therapy After Shoulder Stabilization Surgery · NA · completed
- NCT04902274 — Effectiveness of Transcranial Direct Current Stimulation (tDCS). · NA · terminated
- NCT04269473 — Video Telehealth Gait Retraining for Running-Related Knee Pain · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03525275 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Keller Army Community Hospital
- Last refreshed: 20 May 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03525275.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing