Shoulder InjuriesNCT04749472
Biomechanical Analysis of Scapula and Humerus With Different Shoulder Slings
A study testing Sling in people with Shoulder Injuries and Surgery, run by Hacettepe University at 1 site in Turkey (Türkiye).
Trial summary
Participants will be measured with motion monitor system while using 6 different slings. Measurement order will be randomized, and 5 minutes resting period will be given prior measurement. Scapula, humerus and thorax positions will be recorded in resting position and then with slings. Read more about this study
- Who is it for?
- Ages 18 to 30 yearsHealthy volunteers can take part
- Conditions the study is for
- Shoulder Injuries, Surgery
- What is being tested?
- Sling
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 15 Feb 2021to 20 Dec 2022
- Phase
- Interventional
- 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 30 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- -
Who cannot join
- Having a shoulder surgery
- Having scapular dyskinesis,
- Having shoulder pain,
- Having any disease that could affect posture and/or shoulder (such as scoliosis)
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Hacettepe University
Ankara, 06100
İrem Duzgun, Prof., +903123051576, iremduzgun@yahoo.com
About this study
Participants will be measured with motion monitor system while using 6 different slings. Measurement order will be randomized, and 5 minutes resting period will be given prior measurement. Scapula, humerus and thorax positions will be recorded in resting position and then with slings.
- Conditions
- Shoulder Injuries, Surgery
- Being tested
- Sling
- Keywords
- Rehabilitation, Shoulder Surgery, Postoperative
- Medical subject headings
- Shoulder Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SlingOther
Participants wore six different shoulder slings in a randomized order.
| Study group | Role | What they receive |
|---|---|---|
| Study Group | Experimental | Participants received intervention. Receives: Other: Sling |
What is being measured
The primary outcome is the main question the study is designed to answer.
Motion Monitor
Motion monitor device was used to analyze 3D positions of the arm, shoulder, scapula and thorax.
Measured: During rest position without and with different slings for 5 seconds.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Feb 2021
- Study start15 Feb 2021 (estimated)
- Primary completion12 Sep 2022 (estimated)
- Study completion20 Dec 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Shoulder InjuriesStudies of the same condition, open and under way.
- More trials run by Hacettepe UniversityThe 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Participants wore different sling in a randomized order.
- Masking
- None (open label)
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hacettepe University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Elif Turgut, Hacettepe University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04749472
- Sponsor's protocol ID
- HUSportsSling
- Status last verified
- Feb 2021
- First submitted
- 7 Feb 2021
- Last updated
- 11 Feb 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 11 Feb 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Biomechanical Analysis of Scapula and Humerus With Different Shoulder Slings
- ClinicalTrials.gov ID
- NCT04749472
- Acronym / sponsor ID
- HUSportsSling
- Conditions
- Shoulder Injuries, Surgery
- Keywords
- Rehabilitation, Shoulder Surgery, Postoperative
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- Hacettepe UniversityUniversity, hospital or other
- Study start
- 15 Feb 2021 (estimated)
- Primary completion
- 12 Sep 2022 (estimated)
- Study completion
- 20 Dec 2022 (estimated)
- First posted
- 11 Feb 2021 (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.
Participants will be measured with motion monitor system while using 6 different slings. Measurement order will be randomized, and 5 minutes resting period will be given prior measurement. Scapula, humerus and thorax positions will be recorded in resting position and then with slings.
Study design
- Primary purpose
- Basic science
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Participants wore different sling in a randomized order.
| Arm | Type | Receives |
|---|---|---|
| Study Group | Experimental | Other: SlingParticipants received intervention. |
Who may qualify
- Ages
- 18 to 30 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (1 listed)
- -
Key exclusion criteria (4 listed)
- Having a shoulder surgery
- Having scapular dyskinesis,
- Having shoulder pain,
- Having any disease that could affect posture and/or shoulder (such as scoliosis)
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 |
|---|---|---|
| SlingParticipants wore six different shoulder slings in a randomized order. | Other | Study Group |
Primary outcome
Motion Monitor
Time frame: During rest position without and with different slings for 5 seconds.
Motion monitor device was used to analyze 3D positions of the arm, shoulder, scapula and thorax.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Feb 2021.
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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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Sling in people with Shoulder Injuries and Surgery, run by Hacettepe University at 1 site in Turkey (Türkiye).
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 1 inclusion and 4 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: status not confirmed, as of the sponsor's last update on 11 Feb 2021. 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 Turkey (Türkiye). 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Elif Turgut, Assoc Prof. (+905442645600, elif.turgut.pt@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Motion Monitor (time frame: During rest position without and with different slings for 5 seconds.). 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 11 Feb 2021.