Effectiveness of an ankle injury prevention program for new army recruits
Ankle Injuries, Imaging and Prevention Program Effectiveness in New Army Recruits
This study tests if a special exercise program can help prevent ankle injuries in new army recruits aged 18-23 during their training.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 700 (estimated) |
| Ages | 18 Years to 22 Years |
| Sex | Male |
| Sponsor | University of Haifa Academic / other |
| Locations | 1 site (Netanya) |
| Trial ID | NCT06469099 on ClinicalTrials.gov |
What this trial studies
This study evaluates ankle injuries among new infantry recruits by assessing their musculoskeletal health and the effectiveness of a preventive exercise program. A total of 650 male soldiers aged 18-23 will undergo various assessments at the start and end of their military training, including evaluations of proprioception, balance, muscle strength, and ankle stability. Following these assessments, the recruits will participate in a daily ankle sprain prevention exercise program for six months, with a concluding evaluation to measure outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are male infantry recruits aged 18-23 who are beginning their military training.
Not a fit: Patients with known bone diseases or those who have undergone orthopedic surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly reduce the incidence of ankle injuries among new recruits, enhancing their overall physical performance and readiness.
How similar studies have performed: Previous studies have shown success with similar preventive exercise programs in reducing injury rates in athletic populations.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * soldiers ages 18-22 Exclusion Criteria: * knows disease of the bones * before orthopedic surgery
Where this trial is running
Netanya
- The Academic college Levinsky-Wingate at the Wingate Institute — Netanya, Israel (Recruiting)
Study contacts
- Principal investigator: Gali Dar, Prof. — University of Haifa
- Study coordinator: Gali Dar, Prof
- Email: galidar@yahoo.com
- Phone: 0505662054
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.