Sport InjurySPASBNCT04641520
Shoulder Profile Among Swimmers and Badminton Players
An observational study of Sport Injury and Shoulder Injuries, run by University Hospital, Caen at 1 site in France.
Trial summary
Background: To compare the pre-season clinical measures with shoulder rotator strength and range of motion between bilateral (swimmers) and unilateral (badminton players) overhead athletes. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Sport Injury, Shoulder Injuries
- What is being tested?
- Shoulder clinical testing with isokinetic strength assessment
- How many people
- 42 participants
- Where
- 1 siteFrance
- Study dates
- 1 Sep 2017to 15 Nov 2019
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Elite swimmers and badminton players
Who may be able to join
- All the elite badminton players from a high-level club and the National Institute of Sport, Expertise, and Performance
- All the elite swimmers a high-level club
Who cannot join
- Players who had SSI in the 3 months prior to the isokinetic test or had shoulder surgery
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Comparative Study on Shoulder Rotational Strength and Range of Motion Between Unilateral and Bilateral Overhead Elite Athletes
Background: To compare the pre-season clinical measures with shoulder rotator strength and range of motion between bilateral (swimmers) and unilateral (badminton players) overhead athletes. Design: Prospective cohort study Participants: 42 athletes were enrolled including 24 elite badminton players and 18 elite swimmers Independent variables: A pre-season visit consisted in clinical and isokinetic shoulder strength testing. Clinical testing consisted in the shoulder range of motion (ROM) measurements aIsokinetic internal and external rotator shoulder muscles strength was tested at 60. Conventional and functional (eccentric-to-concentric) ratios (FR) were calculated.
- Conditions
- Sport Injury, Shoulder Injuries
- Being tested
- Shoulder clinical testing with isokinetic strength assessment
- Medical subject headings
- Shoulder Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Shoulder clinical testing with isokinetic strength assessmentOther
All the participants had a shoulder clinical testing including shoulder rotators range of motion and isokinetic rotator muscle strength testing
What is being measured
The primary outcome is the main question the study is designed to answer.
Baseline Isokinetic strength testing (peak torques)
Shoulder rotator muscles isokinetic strength test, Measures: Peak Torque on internal rotator muscles (IR) and external rotator muscles (ER), in NM (newton.meter)
Measured: one preseason evaluation (september 2017 or september 2018 or september 2019)
Baseline Isokinetic strength testing (ratios)
Shoulder rotator muscles isokinetic strength test, Measures: ratios between external rotator muscles (ER) and internal rotator muscles (IR) (ER:IR), in percent (%)
Measured: one preseason evaluation (september 2017 or september 2018 or september 2019)
Clinical measurements, ROM
Shoulder internal and external rotation range of motion (ROM)
Measured: one preseason evaluation (september 2017 or september 2018 or september 2019)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Nov 2020
- Study start1 Sep 2017
- Primary completion1 Nov 2017
- Study completion15 Nov 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Sport InjuryStudies of the same condition, open and under way.
- More trials run by University Hospital, CaenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 42 participants (actual)
Sponsor and investigators
- Lead sponsor
- University Hospital, Caen
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Joffrey DRIGNY, University Hospital, Caen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04641520
- Sponsor's protocol ID
- SPASB
- Acronym
- SPASB
- Status last verified
- Nov 2020
- First submitted
- 18 Nov 2020
- Last updated
- 23 Nov 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 23 Nov 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Comparative Study on Shoulder Rotational Strength and Range of Motion Between Unilateral and Bilateral Overhead Elite Athletes
- ClinicalTrials.gov ID
- NCT04641520
- Acronym / sponsor ID
- SPASB / SPASB
- Conditions
- Sport Injury, Shoulder Injuries
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 42 participants (actual)
- Lead sponsor
- University Hospital, CaenUniversity, hospital or other
- Study start
- 1 Sep 2017 (actual)
- Primary completion
- 1 Nov 2017 (actual)
- Study completion
- 15 Nov 2019 (actual)
- First posted
- 23 Nov 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Background: To compare the pre-season clinical measures with shoulder rotator strength and range of motion between bilateral (swimmers) and unilateral (badminton players) overhead athletes. Design: Prospective cohort study Participants: 42 athletes were enrolled including 24 elite badminton players and 18 elite swimmers Independent variables: A pre-season visit consisted in clinical and isokinetic shoulder strength testing. Clinical testing consisted in the shoulder range of motion (ROM) measurements aIsokinetic internal and external rotator shoulder muscles strength was tested at 60. Conventional and functional (eccentric-to-concentric) ratios (FR) were calculated.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Elite swimmers and badminton players
Key inclusion criteria (2 listed)
- All the elite badminton players from a high-level club and the National Institute of Sport, Expertise, and Performance
- All the elite swimmers a high-level club
Key exclusion criteria (1 listed)
- Players who had SSI in the 3 months prior to the isokinetic test or had shoulder surgery
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Shoulder clinical testing with isokinetic strength assessmentAll the participants had a shoulder clinical testing including shoulder rotators range of motion and isokinetic rotator muscle strength testing | Other | – |
Primary outcome
Baseline Isokinetic strength testing (peak torques)
Time frame: one preseason evaluation (september 2017 or september 2018 or september 2019)
Shoulder rotator muscles isokinetic strength test, Measures: Peak Torque on internal rotator muscles (IR) and external rotator muscles (ER), in NM (newton.meter)
Baseline Isokinetic strength testing (ratios)
Time frame: one preseason evaluation (september 2017 or september 2018 or september 2019)
Shoulder rotator muscles isokinetic strength test, Measures: ratios between external rotator muscles (ER) and internal rotator muscles (IR) (ER:IR), in percent (%)
Clinical measurements, ROM
Time frame: one preseason evaluation (september 2017 or september 2018 or september 2019)
Shoulder internal and external rotation range of motion (ROM)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Nov 2020.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Sport Injury and Shoulder Injuries, run by University Hospital, Caen at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 23 Nov 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Baseline Isokinetic strength testing (peak torques) (time frame: one preseason evaluation (september 2017 or september 2018 or september 2019)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Nov 2020.