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Clinical Trials/NCT06717477
NCT06717477
Enrolling By Invitation
Not Applicable

Streamlining Care for Patients With Compression Neuropathies: The Carpal Tunnel Plus Pathway

University of British Columbia1 site in 1 country200 target enrollmentFebruary 18, 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Carpal Tunnel Syndrome (CTS)
Sponsor
University of British Columbia
Enrollment
200
Locations
1
Primary Endpoint
Wait times
Status
Enrolling By Invitation
Last Updated
4 months ago

Overview

Brief Summary

The goal of this clinical trial is to assess the impact of a new care pathway (the Carpal Tunnel Plus Pathway) in patients with carpal tunnel syndrome. The main questions it aims to answer are:

  1. What was the effect of the Carpal Tunnel Plus Pathway on wait times between each step of the care pathway (e.g. from referral to initial consult, from initial consult to surgical consult, etc.)?
  2. How satisfied are patients with the care they received through the Carpal Tunnel Plus Pathway?

Researchers will compare wait times pre- and post- Pathway implementation to see if there was any change.

Participants will be asked to complete a short patient satisfaction survey.

Registry
clinicaltrials.gov
Start Date
February 18, 2025
End Date
March 1, 2026
Last Updated
4 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kristine Chapman

Clinical Professor

University of British Columbia

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older
  • Referred to the Vancouver General Hospital Neuromuscular Disease Unit or St. Paul's Hospital with a confirmed diagnosis of carpal tunnel syndrome
  • Ability to understand English

Exclusion Criteria

  • Inability to provide informed consent

Outcomes

Primary Outcomes

Wait times

Time Frame: From initial referral to surgery/injection (variable, but approximately 9 months)

Time between each step of the care pathway (e.g. from referral to EMG/neurologic consultation, from referral to surgical consultation, from surgical consultation to surgery)

Patient satisfaction

Time Frame: Immediately after surgery/injection appointment

Patients will be asked to complete a short questionnaire to indicate their level of satisfaction with the care that they received. The custom survey will consist of 4 questions on various aspects of their care that participants will rate on a scale of 1-5 (1 = not at all satisfied, 5 = very satisfied).

Study Sites (1)

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