Barriers and Facilitators in Radiographic Devices and Imaging
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorWestern University
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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 informed consent
Disqualifiers
Responses will be excluded if answered in under two minutes, contained short repossess to open-ended questions or are flagged by Qualtrics bot detection
Trial population
Participants consist of MRTs based in North America.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Survey using a questionnaire.
Other interventionQuestionnaire regarding barriers and facilitators of the implementation of a radiographic positioning device.
Treatment groups
500 Participants
are divided into 1 treatment groupGroup A: Medical Radiation Technologists/X-ray Professionals1 intervention
Trial outcomes
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.Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: