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

• Sponsor: Hillel Yaffe Medical Center (Other)
• Overall Status: Unknown status
• CT.gov ID: NCT02654275
• Collaborator: Wingate College (Other)
• Enrollment: 100
• Location: 1
• Arms: 2
• Duration (Months): 12
• Patients Per Site Per Month: 8.3

Study Details

Study Description

Brief 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.

Condition or Disease	Intervention/Treatment	Phase
Injury Prevention	Other: Proprioceptive Intervention	N/A

Study Design

• Study Type: Interventional
• Anticipated Enrollment: 100 participants
• Allocation: Non-Randomized
• Intervention Model: Parallel Assignment
• Masking: None (Open Label)
• Primary Purpose: Prevention
• Study Start Date: Feb 1, 2016
• Anticipated Primary Completion Date: Feb 1, 2017
• Anticipated Study Completion Date: Feb 1, 2017

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: Proprioceptive Intervention Strength training on a non-stable surface	Other: Proprioceptive Intervention
No Intervention: No Proprioceptive Intervention Conventional strength training

Outcome Measures

Primary Outcome Measures

1. Change in proprioceptive ability [8 weeks]

   Biodex Device which measures joint proprioceptive ability, will measure the change before and after training

Secondary Outcome Measures

1. Change in muscle strength [8 weeks]

   Biodex Device will measure the change in muscle isokinetic strength before and after training

Eligibility Criteria

Criteria

• Ages Eligible for Study: 10 Years to 20 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Healthy

• Swim 3 times per week

Exclusion Criteria:

• Have not had orthopedic surgery

• No history of disease

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Wingate College	Netanya		Israel

Sponsors and Collaborators

• Hillel Yaffe Medical Center
• Wingate College

Investigators

• Principal Investigator: Eias Kassem, MD, Hillel Yaffe Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Hillel Yaffe Medical Center
• ClinicalTrials.gov Identifier: NCT02654275
• Other Study ID Numbers: 17-15-HYMC
• First Posted: Jan 13, 2016
• Last Update Posted: Jan 13, 2016
• Last Verified: Jan 1, 2016

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No

Study Results

No Results Posted as of Jan 13, 2016