- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07766239
Barriers and Facilitators in Radiographic Devices and Imaging
10. august 2026 opdateret af: Emily Lalone, Western University
Perceived Barriers and Facilitators Among Radiation Technologists of Radiographic Device Implementation in North America
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.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Observationel
Tilmelding (Anslået)
500
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Emily Lalone, PhD
- Telefonnummer: 88243 519-661-2111
- E-mail: emily.lalone@uwo.ca
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ja
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Participants consist of MRTs based in North America.
Beskrivelse
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 informed consent
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
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
Medical Radiation Technologists/X-ray Professionals
Medical Radiation Technologists (MRTs) or other health professionals responsible for performing x-rays based in North America.
|
Questionnaire regarding barriers and facilitators of the implementation of a radiographic positioning device.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Implementation Outcomes
Tidsramme: 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.
|
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).
|
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.
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
1. august 2026
Primær færdiggørelse (Anslået)
1. september 2027
Studieafslutning (Anslået)
1. april 2028
Datoer for studieregistrering
Først indsendt
2. august 2026
Først indsendt, der opfyldte QC-kriterier
10. august 2026
Først opslået (Faktiske)
14. august 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
14. august 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
10. august 2026
Sidst verificeret
1. juli 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 129286
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
IPD-planbeskrivelse
Participants will remain anonymous with their data visible to the study team only.
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .