Mobile Application Utilization for Measurement of Scapular Position
Status: | Completed |
---|---|
Conditions: | Orthopedic |
Therapuetic Areas: | Orthopedics / Podiatry |
Healthy: | No |
Age Range: | 18 - 65 |
Updated: | 3/23/2019 |
Start Date: | June 2016 |
End Date: | January 2019 |
1) Mobile Application Utilization for Measurement of Scapular Position 2) 3D Shoulder Motion Measurement Device (The MnMotion System)
The purpose of this study is to determine the ability of a mobile clinical application to
reliably and accurately track scapular motion in people with asymptomatic and symptomatic
shoulders. The ability to accurately and reliably measure shoulder position clinically is an
important first step in choosing the best treatment techniques to treat shoulder movement
dysfunction. Therefore, the primary objectives of the study are:
1. To determine the inter- and intra-rater reliability of shoulder joint position
measurements in symptomatic and asymptomatic subjects, by using a mobile application,
with and without use of a handle for a smartphone
2. To determine the validity of the shoulder joint position measurements measurements as
described above.
reliably and accurately track scapular motion in people with asymptomatic and symptomatic
shoulders. The ability to accurately and reliably measure shoulder position clinically is an
important first step in choosing the best treatment techniques to treat shoulder movement
dysfunction. Therefore, the primary objectives of the study are:
1. To determine the inter- and intra-rater reliability of shoulder joint position
measurements in symptomatic and asymptomatic subjects, by using a mobile application,
with and without use of a handle for a smartphone
2. To determine the validity of the shoulder joint position measurements measurements as
described above.
Subjects will be asked to provide demographic and background information such as age, height,
history of pain or injury, and descriptions of their physical activity levels. Subjects will
receive a clinical screening exam by a licensed physical therapist to determine the type of
movement abnormalities present, the severity of their symptoms and to screen for inclusion
and exclusion criteria.
To collect scapular position measurement reliability data, subjects will stand through out
data collection. Measurements of the scapula will be taken with the mobile application for
the arm at rest and in two elevated position. Subjects will wear an off-the-shelf elbow brace
when asked to hold their arm in the two elevated positions. These elevated positions will be
maintained by having subjects maintain contact of their forearm against a guide. For
intra-rater reliability, position measurements will be repeated twice for each of three
planes of elevation. Additionally, for inter-rater reliability each measurement will be
repeated once by two other examiners. This process will repeated twice when using the
application with and without the handle.
For the validation portion of the study, a subgroup of subjects will have the same position
measurements performed by a single examiner with additional motion sensors taped to the skin
of their scapula and breast bone and a sensor attached to an arm brace strapped to their arm.
In total, the subject will be asked to raise and hold their arm for approximately 5 sec, 36
times during the testing within ranges of motion typically performed during daily activities.
history of pain or injury, and descriptions of their physical activity levels. Subjects will
receive a clinical screening exam by a licensed physical therapist to determine the type of
movement abnormalities present, the severity of their symptoms and to screen for inclusion
and exclusion criteria.
To collect scapular position measurement reliability data, subjects will stand through out
data collection. Measurements of the scapula will be taken with the mobile application for
the arm at rest and in two elevated position. Subjects will wear an off-the-shelf elbow brace
when asked to hold their arm in the two elevated positions. These elevated positions will be
maintained by having subjects maintain contact of their forearm against a guide. For
intra-rater reliability, position measurements will be repeated twice for each of three
planes of elevation. Additionally, for inter-rater reliability each measurement will be
repeated once by two other examiners. This process will repeated twice when using the
application with and without the handle.
For the validation portion of the study, a subgroup of subjects will have the same position
measurements performed by a single examiner with additional motion sensors taped to the skin
of their scapula and breast bone and a sensor attached to an arm brace strapped to their arm.
In total, the subject will be asked to raise and hold their arm for approximately 5 sec, 36
times during the testing within ranges of motion typically performed during daily activities.
Inclusion Criteria:
1. Asymptomatic subjects: subjects without complaints or history of shoulder pain or
obvious movement abnormalities.
2. Symptomatic subjects: subjects with shoulder pain who have active range of motion
beyond 120° of elevation.
Exclusion Criteria:
1. Symptomatic and asymptomatic subjects: history of trauma including fractures,
dislocations, previous shoulder surgeries within the past 6 weeks. Humeral elevation
less than 120 degrees, shoulder symptomology that is judged by the examiner to be of
cervical origin.
2. Asymptomatic subjects: Complaints of shoulder pain, positive results on joint tests
commonly associated with shoulder impingement, presence of shoulder joint movement
abnormalities as determined by a physical therapist, including thoracic scoliosis.
We found this trial at
1
site
Minneapolis, Minnesota 55455
(612) 625-5000

Principal Investigator: Paula Ludewig, PhD, PT
Phone: 612-625-4751
Univ of Minnesota With a flagship campus in the heart of the Twin Cities, and...
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