NCT02654275

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2016

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 11, 2016

Completed
2 days until next milestone

First Posted

Study publicly available on registry

January 13, 2016

Completed
19 days until next milestone

Study Start

First participant enrolled

February 1, 2016

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2017

Completed
Last Updated

January 13, 2016

Status Verified

January 1, 2016

Enrollment Period

1 year

First QC Date

January 11, 2016

Last Update Submit

January 11, 2016

Conditions

Injury Prevention

Outcome Measures

Primary Outcomes (1)

  • Change in proprioceptive ability

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

    8 weeks

Secondary Outcomes (1)

  • Change in muscle strength

    8 weeks

Study Arms (2)

Proprioceptive Intervention

ACTIVE COMPARATOR

Strength training on a non-stable surface

Other: Proprioceptive Intervention

No Proprioceptive Intervention

NO INTERVENTION

Conventional strength training

Interventions

Proprioceptive InterventionOTHER
Proprioceptive Intervention

Eligibility Criteria

Age10 Years - 20 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Healthy
  • Swim 3 times per week

You may not qualify if:

  • Have not had orthopedic surgery
  • No history of disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Wingate College

Netanya, Israel

Location

Study Officials

  • Eias Kassem, MD

    Hillel Yaffe Medical Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Nili Steinberg, PhD

CONTACT

972-9-8639245knopp@wincol.ac.il

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 11, 2016

First Posted

January 13, 2016

Study Start

February 1, 2016

Primary Completion

February 1, 2017

Study Completion

February 1, 2017

Last Updated

January 13, 2016

Record last verified: 2016-01

Data Sharing

IPD Sharing
Will not share

Locations

IL(1)