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NCT02654275 Clinical Trial

Effect of Proprioceptive Intervention Training on Power Capacity, Proprioceptive Ability and Technique of Young Swimmers

Injury Prevention Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT02654275
Other study ID # 17-15-HYMC
Secondary ID
Status Not yet recruiting
Phase N/A
First received January 11, 2016
Last updated January 11, 2016
Start date February 2016
Est. completion date February 2017

Study information
Verified date January 2016
Source Hillel Yaffe Medical Center
Contact Nili Steinberg, PhD
Phone 972-9-8639245
Email knopp@wincol.ac.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

Many children and adolescents who engage in swimming complain of shoulder pain during or after exercise. This pain may worsen and may lead to a decline in performance as well avoidance of swimming and lastly avoidance of any physical activity whatsoever. The aim of this study is to determine whether proprioceptive intervention training will effect the power capacity, proprioceptive ability and technique of young swimmers.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 100
Est. completion date February 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender Both
Age group 10 Years to 20 Years
Eligibility Inclusion Criteria:

- Healthy

- Swim 3 times per week

Exclusion Criteria:

- Have not had orthopedic surgery

- No history of disease

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Other:
• Proprioceptive Intervention

Locations
Country Name City State
Israel Wingate College Netanya

Sponsors (2)
Lead Sponsor Collaborator
Hillel Yaffe Medical Center Wingate College

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in proprioceptive ability Biodex Device which measures joint proprioceptive ability, will measure the change before and after training 8 weeks No
Secondary Change in muscle strength Biodex Device will measure the change in muscle isokinetic strength before and after training 8 weeks No
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