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

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

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07580976
Enrollment
1800
Registered
2026-05-12
Start date
2026-06-14
Completion date
2027-09-01
Last updated
2026-05-18

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

Conditions

Arthritis, Trauma (Including Fractures)

Brief 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.

Interventions

DEVICETru Vu tool and training

A positioning aid and training videos for wrist x-rays

Sponsors

Western University
Lead SponsorOTHER
Newfoundland Health Services
CollaboratorUNKNOWN
NLHS
CollaboratorUNKNOWN

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Must be 18 years of age or older * Must be proficient in English (reading/writing) * Must have been referred for wrist imaging at one of the following healthcare centers: Health Sciences Center (St. John's, NL), Bonne Bay Health Center (Norris Point, NL), or Labrador Health Center (Happy Valley-Goose Bay, NL).

Exclusion criteria

* Incapable of providing informed consent

Design outcomes

Primary

MeasureTime frameDescription
Radiograph grading scoreRadiographs will be collected retrospectively 4 months prior to implementation and 6 months prospectively after the implementation of the tool.Radiographs collected retrospectively and prospectively will be graded by a radiologist and radiographer
Tool adoption (and associated implementation outcomes)The survey will be administered 6 months after the implementation of the tool and training.A survey will collect perceived tool use and other perceived implementation outcomes (including fidelity, appropriateness, acceptability, and adoption).

Secondary

MeasureTime frameDescription
Sustainability6 months after the conclusion of the implementation periodPost-follow up survey will be conducted 6 months after the end of the implementation period and will collect perceived tool use.
Repeated radiographsRepeat radiographs will be collected and compared 4 months retrospectively prior to implementation and 6 months after the start of implementation.Document the number of repeat radiographs captured.

Countries

Canada

Contacts

CONTACTEmily Lalone, PhD
emily.lalone@uwo.ca519-661-2111

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 19, 2026