Achilles tendon disorder
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Members of the Gunma University School of Medicine Track and Field Team 2. Individuals with no history of orthopedic conditions affecting the lower limbs within the past three months 3. Individuals who can undergo measurement using an ultrasound imaging device 4. Individuals who have received an explanation of this study and have provided informed consent
Exclusion criteria
Exclusion criteria: 1. Individuals with a history of surgery on the foot or around the ankle 2. Individuals with a history of Achilles tendon rupture 3. Individuals with less than six months of athletic activity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation/Measurement Timepoints: Before exercise intervention, Immediately after exercise intervention, 6 hours after exercise intervention, 24 hours after exercise intervention, 48 hours after exercise intervention, 72 hours after exercise intervention Primary Outcome: Cross-sectional Area (CSA) | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation/Measurement Timepoints: Pre-exercise intervention, Immediately post-exercise intervention, 6 hours post-exercise intervention, 24 hours post-exercise intervention, 48 hours post-exercise intervention, 72 hours post-exercise intervention Secondary Outcomes: Tendon thickness, fibrillar pattern, brightness distribution, dynamic creep response (change in free Achilles tendon length), gastrocnemius thickness, passive ankle dorsiflexion range of motion, isometric ankle plantar flexion strength, basic information (height, weight, gender, age), athletic history, training status, recovery time for each item | — |
Countries
Japan
Contacts
Gunma University Graduate School Graduate School of Health Sciences, Department of Health Sciences