Barriers to Routine Surgical Video Recording

Status Completed

Clinical Trial Summary

In order to improve the implementation of routine surgical video recording, the researchers want to understand what the challenges associated with the uptake of this technology are. The aim of this study is to explore the barriers faced by key stakeholders including the surgical care team, information governance, and patients within the field of surgical video reporting. The data from this qualitative study will allow the researchers to understand better the challenges associated with uptake of surgical video recording. This will allow the researchers to develop strategies to overcome these challenges and subsequently improve uptake of surgical video recording which will promote safer and more transparent surgery.

Clinical Trial Description

This study will involve the use of interviews to determine the barriers to the implementation of surgical video recording. 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06385210
Study type	Interventional
Source	Imperial College London
Contact
Status	Completed
Phase	N/A
Start date	April 1, 2024
Completion date	April 24, 2024

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT01114971` - Labetalol and Esmolol: Vital Signs and Post Operative Pain Management	Phase 4
Completed	`NCT05624346` - The Effect of Respiratory Exercise After Laparoscopic Surgery	N/A
Not yet recruiting	`NCT04999696` - Minimally Invasive Therapy Versus Open Radical Hysterectomy for Management of Early Stage Cervical Cancer	N/A
Completed	`NCT01084200` - Comparison of Sevoflurane, Propofol, and Sevoflurane Plus Propofol for Maintenance of Anaesthesia	Phase 4
Not yet recruiting	`NCT00731107` - XCEL Bladeless Trocar Versus Veress Needle: A Randomised Controlled Trial Comparing These Two Entry Techniques in Gynaecological Laparoscopic Surgery.	N/A
Not yet recruiting	`NCT06050161` - Evaluating Artisential Laparoscopic Instruments in Gynecologic Surgery	N/A
Recruiting	`NCT05005117` - Laparoscopic Approach for Emergency Colon Resection	N/A
Recruiting	`NCT05436899` - A Pilot Study on Training Simulator Efficacy	N/A
Recruiting	`NCT05542823` - Effect of Cuff Pressure of Endotracheal Tube on POST
Terminated	`NCT03684304` - The Effect of Abdominal Binder Use on Postoperative Pain and Mobility in Patients Undergoing Pelvic Surgery	N/A
Completed	`NCT04146090` - Low-pressure vs Standard-pressure in Laparoscopic Cholecystectomy	N/A
Terminated	`NCT01436032` - Efficacy, Safety and Tolerability Study of N1539 in Subjects After Abdominal Laparoscopic Surgery	Phase 3
Active, not recruiting	`NCT05109130` - Change of Circulating Tumor Cells During Laparoscopic or Transanal Endoscopic Surgery for Rectal Cancer.
Completed	`NCT04642118` - Low-pressure Pulmonary Recruitment Maneuver to Decrease Post-laparoscopic Shoulder Pain in Gynecologic Surgery	N/A
Recruiting	`NCT06150079` - Individualized PEEP Titration on Postoperative Pulmonary Complications	N/A
Completed	`NCT05121454` - Validation of Serenno CUO and IAP Measuring Device
Not yet recruiting	`NCT05092425` - Analysis of Risk Factors for Children With Heterochronous Indirect Hernia
Recruiting	`NCT03318185` - Gasless Single-port Laparoscopic-assisted Radical Resection for Rectal Carcinoma	N/A
Completed	`NCT03506555` - Laparoscopic Access in General Surgery: the Closed (Veress Needle) Technique Versus the Open (Hasson) Technique	N/A
Recruiting	`NCT06338865` - Short Title: Standard vs. Lower Pressure Pneumoperitoneum	N/A