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

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

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06717477
Acronym
CTS+ Pathway
Enrollment
200
Registered
2024-12-05
Start date
2025-02-18
Completion date
2026-03-31
Last updated
2025-12-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carpal Tunnel Syndrome (CTS)

Keywords

Carpal Tunnel Syndrome, Patient Satisfaction, Care Pathway

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.

Interventions

PROCEDUREChanges to the care pathway for carpal tunnel syndrome (The Carpal Tunnel Plus Pathway)

Changes to the care pathway for carpal tunnel syndrome. Features of the CTS+ pathway include new referral form, care map for mild, moderate and severe CTS established, point or care ultrasound with steroid injection introduced, and expedited referral to surgeons.

Sponsors

University of British Columbia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Wait timesFrom 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 satisfactionImmediately after surgery/injection appointmentPatients 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).

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026