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Effectiveness of a Neoprene CMC Joint Orthosis

NCT03736252 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 75

Last updated 2019-07-31

No results posted yet for this study

Summary

Patients will be gathered via convenience sample from a hand therapy clinic. They will be provided with a neoprene commercially available orthosis free of charge. Baseline pain and function will be assessed using the VAS and Functional Index of Hand Arthropathies. Four weeks later, pain, function, and patient satisfaction with the device will be gathered using the Quebec User Evaluation of Assistive Technology questionnaire.

Conditions

  • CMC

Interventions

DEVICE

Orthosis provision

Hely and Weber CMC controller

Sponsors & Collaborators

  • Gannon University

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-01
Primary Completion
2019-05-01
Completion
2019-05-01

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 NCT03736252 on ClinicalTrials.gov