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Clinical Trials/NCT02338791
NCT02338791
Completed
Not Applicable

Rehabilitative Ultrasound Imaging: Measurements of Articular Movement of the Shoulder

University of Cincinnati1 site in 1 country105 target enrollmentApril 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Disorder of Shoulder
Sponsor
University of Cincinnati
Enrollment
105
Locations
1
Primary Endpoint
Movement of the humeral head
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to measure the amount of movement between the bones of the shoulder joint when mobilization techniques are applied by a physical therapist.

Detailed Description

The purpose of this study is to image the articular joint movement of the glenohumeral joint utilizing ultrasound imaging (USI). Specific aims include: 1) measurement of the distance between the articular surfaces at rest; 2) measurement of the distance between the articular surfaces during manually applied glides of those surfaces; and 3) analysis of any association between the amount of glide and reported joint mobility, force application, or joint position. Subjects will be recruited from a population of convenience. After consenting to participate, eligible subjects will complete a demographic questionnaire and pretesting of scapular and shoulder mobility. Two days of testing will be scheduled. On the first day, three grades of glenohumeral mobilization will be applied in the following directions: distraction, posterior and inferior. A handheld dynamometer will measure force; ultrasound imaging will record glenohumeral joint position. Each grade and direction will be repeated three times on the right and the left shoulder. On the second day, the mobilizations will be repeated. Measurements of humeral movement will be calculated from the ultrasound images.

Registry
clinicaltrials.gov
Start Date
April 2012
End Date
March 26, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dexter Witt

Associate Professor

University of Cincinnati

Eligibility Criteria

Inclusion Criteria

  • asymptomatic subjects with no history of neck, shoulder, or arm pain; full active pain free range of motion at the cervical spine and shoulders

Exclusion Criteria

  • neuromuscular or musculoskeletal disorders; connective tissue disorders such as rheumatoid arthritis; inflammatory conditions such as Crohns disease; Down's syndrome; Marfan's syndrome; medically diagnosed hypermobility; history of neck, shoulder or arm trauma, pain, or surgery including dislocation and rotator cuff tears; pregnancy; and metal implants

Outcomes

Primary Outcomes

Movement of the humeral head

Time Frame: Immediate measurement of humeral head movement concurrent with application of manual mobilization

The movement of the humeral head in reference to the glenoid fossa is recorded using ultrasound imaging. The amount of movement (as measured in millimeters) between the image taken on rest and the image taken during the manual mobilization is calculated for each direction of manual mobilization. This primary outcome measure is obtained during the performance of the manual mobilization. Subjects are tested and this primary outcome measured during the intervention (manual mobilization) on Day one and, within one week, on Day two. Each subject participates in the study for approximately one week.

Secondary Outcomes

  • Force of Mobilization(Immediate measurement of force used during the application of manual mobilization)

Study Sites (1)

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