ClinicalTrials.gg
Not yet recruitingNCT07766239Updated Aug 14, 2026

Barriers and Facilitators in Radiographic Devices and Imaging

An observational study in Wrist Osteoarthritis, Wrist Fracture and Wrist Injury, sponsored by Western University. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-14.

Sponsored by Western University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
500
Ages
18 Years and older
Sex
All
01

Study summary

This study aims to understand factors that may influence the implementation of a wrist-specific radiographic positioning device in healthcare settings across the United States and Canada. The survey will ask questions about workplace communication, leadership, availability of resources and attitude towards implementing new devices in radiographic imaging. Participants will be MRTs/Radiologic Technologists and they will complete an online questionnaire about current workplace practices and opinions regarding implementation of a new wrist positioning aid. Responses will help identify any potential barriers and facilitators regarding implementation across different healthcare environments.

Read the detailed description

The study research questions are examining implementation determinants such as communication and attitude towards adopting new radiographic technologies. It will examine perceived barriers and facilitators to implementing a new device and consider technologists' willingness to use this type of device in their day-to-day practice. This study will involve the recruitment of medical radiation technologists (MRTs) employed at a healthcare centre in North America (Canada or the United States). MRT Participants will be asked to complete a survey that is designed to evaluate the perceived barriers and facilitators that may affect the implementation of a radiographic positioning device. General information including MRT experience and healthcare centre size and location will be collected along with questions derived from implementation constructs in the Consolidated Framework of Implementation Science. The questionnaire primarily collects quantitative responses with some opportunity for short answers to support responses with quantitative usability data. The results of this survey can provide insight into the ability to implement a radiographic positioning aid within different healthcare centres across North America. Understanding the different barriers and facilitators that may exist and their relationship with healthcare centre size or geographical location can inform the implementation plan of a novel positioning aid.

02

Conditions studied

  • Wrist Osteoarthritis
  • Wrist Fracture
  • Wrist Injury
03

In context

Wrist Fractures

330 studies on the registry are indexed under Wrist Fractures; 73 are open to participants now.

This study's planned enrollment of 500 is above the median of 100 across 53 observational studies indexed under Wrist Fractures.

Browse Wrist Fractures studies →

Lead sponsor

Western University is the lead sponsor of 14 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants consist of MRTs based in North America.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Be 18 years of age or older
  • Be currently employed in the United States or Canada
  • Currently perform or assist with obtaining diagnostic projection radiographs (plain X-rays) as part of their professional responsibilities
  • Provide

Exclusion criteria

Exclusion Criteria:

  • Responses will be excluded if answered in under two minutes, contained short repossess to open-ended questions or are flagged by Qualtrics bot detection
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
500 participants (estimated)
Patient registry
No

Groups and cohorts

  • Medical Radiation Technologists/X-ray Professionals

    Medical Radiation Technologists (MRTs) or other health professionals responsible for performing x-rays based in North America.

    Other: Survey using a questionnaire.

Interventions

  • OtherSurvey using a questionnaire.

    Questionnaire regarding barriers and facilitators of the implementation of a radiographic positioning device.

06

What researchers measure

Primary outcomes

  1. Implementation Outcomes

    Implementation determinants from the Consolidated Framework for Implementation Research (CFIR) will be graded on a questionnaire as being a barrier (0), neutral (1), or a facilitator (2).

    Time frame: Participants can complete the survey at any time. The survey will close after 500 participants complete the survey. It is estimated this will take 1 year. The determinants will be measured at the completion of the survey.

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — Participants will remain anonymous with their data visible to the study team only.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Aug 2026; primary completion for Sep 2027, 13 months later.

Of 20 observational studies under Wrist Fractures, half reached primary completion within 32 months of starting (the median), counting those still running; a quarter within 17 and three quarters within 63. This study's planned 13 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 2, 2026
First posted
Aug 14, 2026
StartEst.
Aug 2026
Primary completionEst.
Sep 2027
CompletionEst.
Apr 2028
Last update
Aug 14, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07766239
Lead sponsor
Western University
Responsible party
Emily Lalone (Associate Professor, Western University) — Principal investigator
First posted
Aug 14, 2026
Start date
Aug 2026 (estimated)
Primary completion
Sep 2027 (estimated)
Completion
Apr 2028 (estimated)
Last update
Aug 14, 2026

Study contacts

Emily Lalone, PhD
Contact
emily.lalone@uwo.ca
519-661-2111 ext. 88243

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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