Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
15 participants
INTERVENTIONAL
2024-04-01
2024-04-24
Brief Summary
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Detailed Description
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Participants will be invited to participate in an online 1 on 1 interview 1 on 1. A total of 10-15 participants will be recruited to interview. Interview guides have been developed from the existing literature on the subject. A member of the research team will be present to conduct all interviews. It is estimated that interviews will last between 45-60mins. All interview audio and video will be recorded, as appropriate.
The aim is to recruit 15 participants of which 2-3 will be patient participants and the remaining will be professional participants.
Concerning recruitment of surgical team members: surgeons; trainees; anaesthetists; nursing staff; and operating department practitioners will be invited to participate. Members of the trust's information governance team will also be recruited as key stakeholders within this field as well as representatives from industry who are known personally to the study team.
Non-patient participants will be identified according to their role and be approached directly in person by a member of the study team at their place of work eg outpatient clinic or operating theatres or invited via email for the purposes of recruitment.
Concerning recruitment of patients, appropriate surgical patients satisfying the study inclusion and exclusion criteria will be identified by the direct care team in an outpatient setting through review of patient records. These patients will be under the direct clinical care of members of the study team and will be patients who are awaiting or have recently undergone surgery. The direct care team will explain the rationale of the study and if the potential participant is willing to be contacted, the direct care team will obtain an email address from the potential participant. The potential participant's email address will then be passed on to the study team for further contact.
All interested participants will be emailed a link to an online participant information sheet and consent form.
Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Semi structured interviews
Semi-structured interviews with topic guides centred around the Non adoption, abandonment, scale-up, spread, and sustainability (NASSS) framework will be led by a member of the research team and conducted with all participants. The aim of the interviews is to explore perceived barriers to the uptake of routine surgical video recording. Transcripts will be subsequently thematically analysed using an inductive approach to determine key themes to the barriers of routine surgical video recording.
Semi structured interviews
Participants will be interviewed concerning perceived barriers to routine surgical video recording
Interventions
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Semi structured interviews
Participants will be interviewed concerning perceived barriers to routine surgical video recording
Eligibility Criteria
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Inclusion Criteria
* Available to online facilities
* Explicitly consented Able to understand and communicate in English
* Aged 18
* On a waiting list for surgery or have previously undergone surgery in the past 3 years
* Access to online (Teams) facilities
* Explicitly consented Able to understand and communicate in English
Exclusion Criteria
* Did not consent to participate
18 Years
ALL
Yes
Sponsors
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Imperial College London
OTHER
Responsible Party
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Locations
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Department of Surgery and Cancer
London, , United Kingdom
Countries
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Other Identifiers
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22SM7855
Identifier Type: -
Identifier Source: org_study_id
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