Strength and EnduranceNCT05536778
Shoulder Endurance Assessment in Upper Limb Athletes
An observational study of Strength and Endurance, run by University of Liege at 1 site in Belgium.
Trial summary
The objective of this study is to explore the relationship between two different "fatigue tests" (Xco Endurance Test and Shoulder Endurance Test) and strength/endurance of shoulder rotators muscles, measured with an isokinetic device. The tests will be organized during two different sessions, in a randomized order. Read more about this study
- Who is it for?
- Ages 18 to 28 years, men only
- Conditions the study is for
- Strength and Endurance
- What is being tested?
- Realization of the 3 tests
- How many people
- 30 participants
- Where
- 1 siteBelgium
- Study dates
- 15 Oct 2022to 15 Apr 2023
- 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 18 to 28 years
- Men only
- Adult
Study population: About 60 people, practicing an overhead sports at least 5 hours a week will be recruited for the study among the sportsclub of the Province of Liège (Belgium)
Who may be able to join
- Age between 18 and 28 years
- To practice an overhead sports, at least 5 hours a week
Who cannot join
- Any shoulder surgery history
- Any shoulder pain
- Any shoulder injury during the last 6 months
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Relation Between Different Tests Aimed to Assess Shoulder Endurance in Upper Limb Athletes
The objective of this study is to explore the relationship between two different "fatigue tests" (Xco Endurance Test and Shoulder Endurance Test) and strength/endurance of shoulder rotators muscles, measured with an isokinetic device.
The tests will be organized during two different sessions, in a randomized order. One session will be dedicated to isokinetic evaluation. The other one will include the performance of the two functional tests.
- Conditions
- Strength and Endurance
- Being tested
- Realization of the 3 tests
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Realization of the 3 testsOther
The participants will have to perform the isokinetic evaluation during one session and the two functional tests during another session. Those sessions will be separated by 14 days.
What is being measured
The primary outcome is the main question the study is designed to answer.
Shoulder rotators strength
Shoulder rotators strength (IR, ER) will be measured with isokinetic dynamometer
Measured: through study completion, 6 months
Shoulder rotators work
Shoulder rotators work (IR, ER) will be measured with isokinetic dynamometer
Measured: through study completion, 6 months
Shoulder Endurance Test
Time until exhaustion (in seconds) will be measured
Measured: through study completion, 6 months
Xco Endurance Test
Time until exhaustion (in seconds) will be measured
Measured: through study completion, 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Sep 2022
- Study start15 Oct 2022
- Primary completion30 Mar 2023
- Study completion15 Apr 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Strength and EnduranceStudies of the same condition, open and under way.
- 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
- Other
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Liege
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Camille Tooth, University of Liege
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05536778
- Sponsor's protocol ID
- Shoulder endurance assessment
- Status last verified
- May 2023
- First submitted
- 29 Aug 2022
- Last updated
- 22 May 2023
- 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 22 May 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Relation Between Different Tests Aimed to Assess Shoulder Endurance in Upper Limb Athletes
- ClinicalTrials.gov ID
- NCT05536778
- Acronym / sponsor ID
- Shoulder endurance assessment
- Conditions
- Strength and Endurance
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- University of LiegeUniversity, hospital or other
- Study start
- 15 Oct 2022 (actual)
- Primary completion
- 30 Mar 2023 (actual)
- Study completion
- 15 Apr 2023 (actual)
- First posted
- 13 Sep 2022 (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.
The objective of this study is to explore the relationship between two different "fatigue tests" (Xco Endurance Test and Shoulder Endurance Test) and strength/endurance of shoulder rotators muscles, measured with an isokinetic device.
The tests will be organized during two different sessions, in a randomized order. One session will be dedicated to isokinetic evaluation. The other one will include the performance of the two functional tests.
Study design
- Observational model
- Cohort
- Time perspective
- Other
Who may qualify
- Ages
- 18 to 28 years
- Sex
- Male only
- Age groups
- Adult
- Study population
- About 60 people, practicing an overhead sports at least 5 hours a week will be recruited for the study among the sportsclub of the Province of Liège (Belgium)
Key inclusion criteria (2 listed)
- Age between 18 and 28 years
- To practice an overhead sports, at least 5 hours a week
Key exclusion criteria (3 listed)
- Any shoulder surgery history
- Any shoulder pain
- Any shoulder injury during the last 6 months
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 |
|---|---|---|
| Realization of the 3 testsThe participants will have to perform the isokinetic evaluation during one session and the two functional tests during another session. Those sessions will be separated by 14 days. | Other | – |
Primary outcome
Shoulder rotators strength
Time frame: through study completion, 6 months
Shoulder rotators strength (IR, ER) will be measured with isokinetic dynamometer
Shoulder rotators work
Time frame: through study completion, 6 months
Shoulder rotators work (IR, ER) will be measured with isokinetic dynamometer
Shoulder Endurance Test
Time frame: through study completion, 6 months
Time until exhaustion (in seconds) will be measured
Xco Endurance Test
Time frame: through study completion, 6 months
Time until exhaustion (in seconds) will be measured
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 22 May 2023.
- 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 Strength and Endurance, run by University of Liege at 1 site in Belgium.
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 3 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 22 May 2023. 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 Belgium. 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?
Shoulder rotators strength (time frame: through study completion, 6 months). The study lists 4 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 22 May 2023.