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ClinicCompanion. Compared to the Use of a Goniometer

NCT ID: NCT02043639

Last Updated: 2024-10-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-08-31

Study Completion Date

2016-02-29

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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Shoulder Impingement Syndrome

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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

Exclusion Criteria

* no use of limbs
* amputees
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Medical Companion LLC

UNKNOWN

Sponsor Role collaborator

Wake Forest University Health Sciences

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Maharaj m Singh, PHD

Role: PRINCIPAL_INVESTIGATOR

Wake Forest University Health Sciences

Navjot m Kohli, MD

Role: PRINCIPAL_INVESTIGATOR

Wake Forest University Health Sciences

Locations

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Aurora St Lukes Medical Center

Milwaukee, Wisconsin, United States

Site Status

Countries

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United States

References

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Mullaney MJ, McHugh MP, Johnson CP, Tyler TF. Reliability of shoulder range of motion comparing a goniometer to a digital level. Physiother Theory Pract. 2010 Jul;26(5):327-33. doi: 10.3109/09593980903094230.

Reference Type BACKGROUND
PMID: 20557263 (View on PubMed)

van de Pol RJ, van Trijffel E, Lucas C. Inter-rater reliability for measurement of passive physiological range of motion of upper extremity joints is better if instruments are used: a systematic review. J Physiother. 2010;56(1):7-17. doi: 10.1016/s1836-9553(10)70049-7.

Reference Type BACKGROUND
PMID: 20500132 (View on PubMed)

MacDermid JC, Chesworth BM, Patterson S, Roth JH. Intratester and intertester reliability of goniometric measurement of passive lateral shoulder rotation. J Hand Ther. 1999 Jul-Sep;12(3):187-92. doi: 10.1016/s0894-1130(99)80045-3.

Reference Type BACKGROUND
PMID: 10459526 (View on PubMed)

Riddle DL, Rothstein JM, Lamb RL. Goniometric reliability in a clinical setting. Shoulder measurements. Phys Ther. 1987 May;67(5):668-73. doi: 10.1093/ptj/67.5.668.

Reference Type BACKGROUND
PMID: 3575423 (View on PubMed)

Khoshelham K, Elberink SO. Accuracy and resolution of Kinect depth data for indoor mapping applications. Sensors (Basel). 2012;12(2):1437-54. doi: 10.3390/s120201437. Epub 2012 Feb 1.

Reference Type BACKGROUND
PMID: 22438718 (View on PubMed)

Dutta T. Evaluation of the Kinect sensor for 3-D kinematic measurement in the workplace. Appl Ergon. 2012 Jul;43(4):645-9. doi: 10.1016/j.apergo.2011.09.011. Epub 2011 Oct 20.

Reference Type BACKGROUND
PMID: 22018839 (View on PubMed)

Other Identifiers

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13-40 ClinicCompanion.

Identifier Type: -

Identifier Source: org_study_id

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