- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06226974
Acute Effects of Static Stretching on the Shoulder Joint Position Sense of Overhead Athletes
February 16, 2024 updated by: University Fernando Pessoa
Acute Effects of Static Stretching on the Shoulder Joint Position Sense of Overhead Athletes: a Randomized Crossover Trial
The purpose of the study is to investigate the acute effects of static stretching on the shoulder joint position sense of overhead athletes.
Study Overview
Detailed Description
A crossover randomized controlled trial will be conducted with 17 overhead athletes (9 males and 8 females).
All of them will perform the 3 study conditions in random order: a control (5-minute rest), and static stretching of 30 or 90 seconds of muscles around the shoulder.
The shoulder joint position sense will be assessed before and immediately after these conditions, and tested by active repositioning for the range of 110º of flexion, with a video camera.
Absolute, relative and variable angular errors will be calculated.
Study Type
Interventional
Enrollment (Actual)
17
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
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Porto, Portugal, 4200-253
- Escola Superior Saúde Fernando Pessoa
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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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Subjects aged between 18 and 30 years
- Competitive overhead athletes (basketball, handball, volleyball, swimming)
- Normal range of motion of flexion of the shoulder
Exclusion Criteria:
- History of injury of the shoulder joint in the previous 6 months
- Positive shoulder joint integrity tests (anterior drawer; fulcrum test; Jerk test; and sulcus sign)
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Condition
5-minute rest.
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Active Comparator: Static Stretching of 30 seconds Condition
Static stretching of 30 seconds of muscles around the shoulder of the dominant upper limb:
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Active Comparator: Static Stretching of 90 seconds Condition
Static stretching of 90 seconds of muscles around the shoulder of the dominant upper limb:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Absolute angular error
Time Frame: Change from Baseline (Before) to Immediately after interventions or control (After)
|
The absolute value of the difference between the target range and the achieved range
|
Change from Baseline (Before) to Immediately after interventions or control (After)
|
|
Relative angular error
Time Frame: Change from Baseline (Before) to Immediately after interventions or control (After)
|
The arithmetic difference between the target range and the range achieved
|
Change from Baseline (Before) to Immediately after interventions or control (After)
|
|
Variable angular error
Time Frame: Change from Baseline (Before) to Immediately after interventions or control (After)
|
The standard deviation of the 3 repositionings
|
Change from Baseline (Before) to Immediately after interventions or control (After)
|
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)
December 1, 2023
Primary Completion (Actual)
January 31, 2024
Study Completion (Actual)
February 15, 2024
Study Registration Dates
First Submitted
January 17, 2024
First Submitted That Met QC Criteria
January 17, 2024
First Posted (Actual)
January 26, 2024
Study Record Updates
Last Update Posted (Estimated)
February 21, 2024
Last Update Submitted That Met QC Criteria
February 16, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- ESS/FSA-374/23-3
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.