Tru-Vu Wrist Positioning Aid Multi-Center Implementation Within NLHS

NCT07580976 · Status: NOT_YET_RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 1800

Last updated 2026-05-18

No results posted yet for this study

Summary

This study has two primary aims: 1) to determine whether a novel wrist x-ray positioning aid can be implemented within 3 different healthcare centers in Newfoundland and Labrador, and 2) to determine the ability of the tool to improve patient positioning in wrist x-rays. It will also learn about the number of repeat x-rays required with or without the use of the tool and radiographer confidence. The main questions it aims to answer are:

1. Will the implementation of the Tru-Vu differ between an urban health center, rural clinic, and remote regional hospital?
2. Can the Tru-Vu improve the positioning procedure for radiographers performing wrist x-rays, resulting with more useful x-rays.

Researchers will compare x-rays before and after the implementation of the tool as well as between centers.

Technologist participants will:

* Use the tool during the positioning procedure for wrist x-rays.
* Provide feedback regarding tool use and perceived implementation barriers and facilitators.

Conditions

Interventions

DEVICE

Tru Vu tool and training

A positioning aid and training videos for wrist x-rays

Sponsors & Collaborators

  • Newfoundland Health Services

    collaborator UNKNOWN
  • NLHS

    collaborator UNKNOWN
  • Western University

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-14
Primary Completion
2027-02-01
Completion
2027-09-01

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

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 NCT07580976 on ClinicalTrials.gov