Testing a new neck training device for injury prevention
Feasibility and Effectiveness of a Novel Neck Training Device: A Pilot Study
This study tests whether using a new neck training device can help active-duty military personnel prevent injuries better than a traditional neck strengthening program.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | All |
| Sponsor | Landstuhl Regional Medical Center Federal |
| Locations | 1 site (Landstuhl, Rheinland Pfalz) |
| Trial ID | NCT06410846 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of the TopSpin360 neck training device over a 12-week period among active-duty military personnel. Participants will be randomly assigned to either the intervention group using the TopSpin360 device or a control group performing a traditional neck strengthening program. The study aims to measure differences in neck strength and performance outcomes, as well as adherence to the training regimen. Data will be collected before and after the intervention to assess the impact of the training on injury prevention.
Who should consider this trial
Good fit: Ideal candidates are healthy active-duty service members aged 18-35 assigned to Landstuhl Regional Medical Center.
Not a fit: Patients with chronic neck issues or those unable to participate fully in physical training may not benefit from this study.
Why it matters
Potential benefit: If successful, this training regimen could significantly reduce the risk of neck injuries and mild traumatic brain injuries in active-duty military personnel.
How similar studies have performed: While similar approaches to injury prevention have been explored, this specific device and training regimen is novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Healthy active-duty service members of any military rank assigned to LRMC * 18-35 years old * assigned to Landstuhl Regional Medical Center * own a personal cellphone to download the TopSpin360 App (intervention group) * able to attend the two times per week training * have sufficient time on station to complete entire study including post-study measures. Exclusion Criteria: * any medical profile that prevents full participation in the ACFT * any chronic inner ear abnormalities (e.g., Meniere's disease or benign positional vertigo) * history of invasive neck procedures (cortisone injections or neck surgery) * any known cervical spine disorders (e.g., degenerative changes of the cervical spine) or gross cervical spine abnormalities when examined by the staff physical therapist * non-US military personnel, i.e., German or Netherlands military personnel etc.
Where this trial is running
Landstuhl, Rheinland Pfalz
- Landstuhl Regional Medical Center — Landstuhl, Rheinland Pfalz, Germany (Recruiting)
Study contacts
- Study coordinator: Christine Olanrewaju, DO
- Email: christine.m.olanrewaju.mil@health.mil
- Phone: 49-06371-9464-5758
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.