- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04432441
Effects of Neuromuscular Electrostimulation on Scapular Stability
November 8, 2021 updated by: Javier Gutiérrez Coronado, University of Extremadura
Effects of Neuromuscular Electrical Stimulation (NMES) Plus Therapeutic Exercise Combination on Scapular Stability in Female Professional Handball Players With Scapular Dyskinesia
Injuries and shoulder pain are common problems in handball, more often among female athletes.
The impact on performance and participation shows the need to work on the risk factors to minimize the damage.
It has been found an association between scapular dysfunction and pain in the shoulder.
Currently there are many exercise programs, but few with electrotherapy implemented.
The aim of the study is to assess the effect of a therapeutic physical exercise program for scapulo-humeral stabilitation with and without electrotherapy on scapular stability, glenohumeral internal rotation and external rotation strength.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
32
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Badajoz, Spain, 06071
- Universidad de Extremadura
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- To have more than 18 YO
- To be female
- To do at least 5 hour of sport training per week in last two years
- To be part of federated club that allows them in their weekly practice to participate in recreational matches or small local championship during weekends.
- To have scapular diskinesis by McClure scale
Exclusion Criteria:
- To have an actual injury
- To have an history of injury in last 12 months
- To take drugs that can affect to control motor.
- To be part or participate in a control motor program or specific prevention program
- To have a recent surgery in last year in upper or back.
- A score below 45 points on the Personal Psychological Apprehension Scale.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Therapeutic physical exercise program for scapulo-humeral stabilitation
|
This group realize a therapeutic physical exercise program for scapulo-humeral stabilitation during a month
|
Active Comparator: Therapeutic physical exercise program for scapulo-humeral stabilitation + Electrostimulation
|
This group realize a therapeutic physical exercise program for scapulo-humeral stabilitation added electrostimulation during a month
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Scapular Static Positioning Assessment: Upper distance
Time Frame: Changes from baseline after a month
|
cm
|
Changes from baseline after a month
|
Scapular Static Positioning Assessment: Lower distance
Time Frame: Changes from baseline after a month
|
cm
|
Changes from baseline after a month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
RI Range of movement
Time Frame: Changes from baseline after a month
|
Degrees
|
Changes from baseline after a month
|
External rotation strenght
Time Frame: Changes from baseline after a month
|
kg
|
Changes from baseline after a month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 15, 2021
Primary Completion (Actual)
February 16, 2021
Study Completion (Actual)
June 11, 2021
Study Registration Dates
First Submitted
June 8, 2020
First Submitted That Met QC Criteria
June 12, 2020
First Posted (Actual)
June 16, 2020
Study Record Updates
Last Update Posted (Actual)
November 16, 2021
Last Update Submitted That Met QC Criteria
November 8, 2021
Last Verified
November 1, 2021
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 19741974
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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