Biomechanical Analysis of Scapula and Humerus With Different Shoulder Slings
Primary Purpose
Shoulder Injuries, Surgery
Status
Unknown status
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Sling
Sponsored by
About this trial
This is an interventional basic science trial for Shoulder Injuries focused on measuring Rehabilitation, Shoulder Surgery, Postoperative
Eligibility Criteria
Inclusion Criteria:
-
Exclusion Criteria:
- Having a shoulder surgery
- Having scapular dyskinesis,
- Having shoulder pain,
- Having any disease that could affect posture and/or shoulder (such as scoliosis)
Sites / Locations
- Hacettepe University
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Study Group
Arm Description
Participants received intervention.
Outcomes
Primary Outcome Measures
Motion Monitor
Motion monitor device was used to analyze 3D positions of the arm, shoulder, scapula and thorax.
Secondary Outcome Measures
Full Information
NCT ID
NCT04749472
First Posted
February 7, 2021
Last Updated
February 7, 2021
Sponsor
Hacettepe University
1. Study Identification
Unique Protocol Identification Number
NCT04749472
Brief Title
Biomechanical Analysis of Scapula and Humerus With Different Shoulder Slings
Official Title
Biomechanical Analysis of Scapula and Humerus With Different Shoulder Slings
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
February 15, 2021 (Anticipated)
Primary Completion Date
September 12, 2022 (Anticipated)
Study Completion Date
December 20, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hacettepe University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Shoulder Injuries, Surgery
Keywords
Rehabilitation, Shoulder Surgery, Postoperative
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Participants wore different sling in a randomized order.
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Study Group
Arm Type
Experimental
Arm Description
Participants received intervention.
Intervention Type
Other
Intervention Name(s)
Sling
Intervention Description
Participants wore six different shoulder slings in a randomized order.
Primary Outcome Measure Information:
Title
Motion Monitor
Description
Motion monitor device was used to analyze 3D positions of the arm, shoulder, scapula and thorax.
Time Frame
During rest position without and with different slings for 5 seconds.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
-
Exclusion Criteria:
Having a shoulder surgery
Having scapular dyskinesis,
Having shoulder pain,
Having any disease that could affect posture and/or shoulder (such as scoliosis)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elif Turgut, Assoc Prof.
Phone
+905442645600
Email
elif.turgut.pt@gmail.com
Facility Information:
Facility Name
Hacettepe University
City
Ankara
ZIP/Postal Code
06100
Country
Turkey
Facility Contact:
First Name & Middle Initial & Last Name & Degree
İrem Duzgun, Prof.
Phone
+903123051576
Email
iremduzgun@yahoo.com
12. IPD Sharing Statement
Learn more about this trial
Biomechanical Analysis of Scapula and Humerus With Different Shoulder Slings
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