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Using Kinect Motion Capture to Measure Shoulder Motion in Patients Undergoing Capsular Distension for Adhesive Capsulitis

NCT04413162 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2025-04-03

No results posted yet for this study

Summary

This study will compare shoulder range of motion assessment using the Kinect motion tracking system vs goniometer in patients with adhesive capsulitis (frozen shoulder) undergoing ultrasound-guided capsular distention procedures (standard of care).

The investigators hypothesize that, for shoulder adhesive capsulitis, the Kinect Motion Analysis 2.0 system will provide reliable results in a shorter and more efficient amount of time in comparison to traditional goniometer methods.

Conditions

  • Adhesive Capsulitis
  • Adhesive Capsulitis of Shoulder
  • Frozen Shoulder
  • Shoulder Frozen
  • Shoulder Pain
  • Mobility Limitation

Interventions

OTHER

Kinect motion tracking system

Kinect motion tracking system is used to measure shoulder range of motion compared to goniometric measurement.

Sponsors & Collaborators

  • University of California, Davis

    lead OTHER

Principal Investigators

  • Kevin Mullins, MD · UC Davis Health

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-06-10
Primary Completion
2025-02-07
Completion
2025-02-07

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04413162 on ClinicalTrials.gov