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Ankle Injuries, Imaging and Prevention Program Effectiveness in New Army Recruits

Ankle Injuries, Imaging and Prevention Program Effectiveness in New Army Recruits

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06469099
Enrollment
786
Registered
2024-06-21
Start date
2024-03-15
Completion date
2025-09-15
Last updated
2026-01-26

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

Conditions

Ankle Sprains

Keywords

soldiers, injury, ankle, exercise

Brief summary

Infantry recruits will undergo a musculoskeletal examination to assess tendon, muscle, proprioception, agility, and joint status. Afterward, an exercise intervention program will be implemented, followed by a concluding evaluation.

Detailed description

Purpose: To evaluate ankle injuries in new infantry recruits, including their characteristics, association with imaging and functional measures, and the effectiveness of a preventive exercise program. Methods: 650 new male infantry soldiers aged 18-23 will be recruited to participate in the study at the beginning of their military training. At the beginning and the end of the training (after approximately six months), the soldiers will be assessed for the following: 1. Demographics (height, weight, leg length, BMI calculation), 2. Proprioception ability (Active Movement Extent Discrimination Apparatus AMEDA), 3. Dynamic balance (Y-Balance Test YBT), 4. Leg muscle strength (bilateral heel rise test), 5. Hip strength (hand-held dynamometer), 6. Ankle agility (hexagon agility hop test), 7. Ankle stability (Anterior Drawer Test, musculoskeletal ultrasound for the Anterior Talofibular Ligament), 8. Achilles tendon structure (Ultrasound tissue Characterization UTC), 9. Aerobic ability (3000 meters run, will be recorded by the fitness instructors at the training base). In addition, the soldiers will fill out a previous ankle sprains questionnaire, pre-induction physical activity questionnaire, the Cumberland Ankle Instability Tool (CAIT) for ankle perceived instability, and the Ankle Fear Avoidance Beliefs Questionnaire (ankle-FABQ). The soldiers will perform a constructed ankle sprain prevention program for five minutes every day during the six-month length of the study. Every 1-2 weeks, the researcher will arrive at the training base to monitor ankle injuries. Those who are diagnosed with a sprain will undergo ultrasound evaluations, which will be performed every few weeks.

Interventions

OTHERexcercises

exercises for strength and balance

Sponsors

University of Haifa
Lead SponsorOTHER
Zinman College of Physical Education and Sports Sciences
CollaboratorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

active soldiers will perform baseline examinations for the musculoskeletal system. following, an exercise intervention program will be conducted with follow-up examination at the termination of program.

Eligibility

Sex/Gender
MALE
Age
18 Years to 22 Years
Healthy volunteers
Yes

Inclusion criteria

* soldiers ages 18-22

Exclusion criteria

* knows disease of the bones * before orthopedic surgery

Design outcomes

Primary

MeasureTime frameDescription
Proprioception abilitybaseline, end of interventionActive Movement Extent Discrimination Apparatus AMEDA
balancebaseline, end of interventionY balance test
Leg muscle strengthbaseline, end of interventionbilateral heel rise test
Hip muscle strengthbaseline, end of interventionhand held dynamometer
Ankle agilitybaseline, end of interventionhexagon agility hop test
Ankle stabilitybaseline, end of interventionAnterior Drawer Test, musculoskeletal ultrasound for the Anterior Talofibular Ligament
Achilles tendon structurebaseline, end of interventionUltrasound tissue Characterization for the percentage of fibers types

Countries

Israel

Contacts

PRINCIPAL_INVESTIGATORGali Dar, Prof.

University of Haifa

Outcome results

None listed

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