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ClinicCompanion. Compared to the Use of a Goniometer

Terminated
Conditions
Shoulder Impingement Syndrome
Registration Number
NCT02043639
Lead Sponsor
Wake Forest University Health Sciences
Brief Summary

In this study, the goal is to find out if the clinicCompanion™ is effective in measuring range of motion when compared to the goniometer. Currently, the goniometer is an approved device to measure range of motion by the FDA, but the clinicCompanion™ is not.

Detailed Description

The study procedure will test the range of motion of the subjects shoulders two different ways: using a goniometer and using the clinicCompanion™. Both tools are designed to measure the degree of movement subjects are able to do. Researchers will take 12 measurements on each arm for each device, for a total of 24 measurements per device. That is a total of 48 measurements for both devices.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • new or established clinic patients from PI's medical practice at Aurora St. Luke's Medical Center
  • 18 years of age and older
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Exclusion Criteria
  • no use of limbs
  • amputees
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Control cost and enhance accuracy of measurementThe goal is to recruit 75 subjects in 18 months

By freeing the doctor from data collection, he or she will be able to spend more time with patient discussing medical conditions and providing pertinent information

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Aurora St Lukes Medical Center

🇺🇸

Milwaukee, Wisconsin, United States

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