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Multimedia Informed Consent & PROMs in Laparoscopic Cholecystectomy (EPICS)

Primary Purpose

Gallstone Disease

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Laparoscopic cholecystectomy
Sponsored by
Nottingham University Hospitals NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Gallstone Disease focused on measuring laparoscopic cholecystectomy

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Male or female.

  • Adults:aged 18 to 85 years.
  • Be referred for consideration for an elective laparoscopic cholecystectomy for symptomatic gallstones based on their GPs diagnosis and referral to a general surgeon.
  • Patients initially listed for laparoscopic cholecystectomy but subsequently converted to open cholecystectomy or subsequently have a more complex 'biliary' procedure (including but not exclusive to bile duct exploration, biliary drain insertion, biliary bypass procedure).

Exclusion Criteria:

  • Patients unable to, or those choosing not to engage with the multimedia process --- including patients lacking mental capacity, patients who do not have access to a multimedia device (including but not exclusive to a computer, tablet or multimedia phone), patients who are unable to use a multimedia device unassisted.
  • Patients who are unable to read or communicate n English without the presence of a translator.
  • Patients undergoing another major non---biliary operation during the same operation as their cholecystectomy.

Sites / Locations

  • Nottingham University Hospitals NHS Trust

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Open Label

Arm Description

Administration of a disease-specific and generic PROMs survey to patients undergoing Laparoscopic Cholecystectomy

Outcomes

Primary Outcome Measures

Mean domain PROMs scores for each study participant
We will look at the change in score between: pre--op and 30-Days, Pre-op and 3 Months post-op and pre-op and 6 months post-op. For this analysis we hope to use the paired t---test, however depending on whether the data is normally distributed or not this may require non---parametric analyses with the Wilcoxon rank---sum test. We also aim to look at the overall trend, which will require analysis of variance.

Secondary Outcome Measures

Completion of the Multimedia Informed Consent package on aboutmyop.org
Completion of the 7---Day follow---up questionnaire.
Completion of a Patient Satisfaction Survey to receive feedback on the process.

Full Information

First Posted
April 25, 2016
Last Updated
February 18, 2020
Sponsor
Nottingham University Hospitals NHS Trust
Collaborators
EIDO Healthcare, The Royal College of Surgeons of England
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1. Study Identification

Unique Protocol Identification Number
NCT02810860
Brief Title
Multimedia Informed Consent & PROMs in Laparoscopic Cholecystectomy
Acronym
EPICS
Official Title
A Study to Pilot the Use of a Multimedia Application to Collect the Largest PROMs (Patient Reported Outcome Measures) Dataset in Adult Patients Undergoing Elective Laparoscopic Cholecystectomy for Symptomatic Gallstones and to Aid the Informed Consent Process
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
August 18, 2016 (Actual)
Primary Completion Date
April 13, 2018 (Actual)
Study Completion Date
January 1, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nottingham University Hospitals NHS Trust
Collaborators
EIDO Healthcare, The Royal College of Surgeons of England

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Collection of PROMs (Patient Reported Outcome Measures) data from patients before and after an operation to remove their gallbladder for the treatment of symptomatic gallstones. This PROMs data will provide information to clinicians and trusts about the health gain following this type of surgery and the impact on patient's quality of life. This information will be collected by the implementation of the patient Website aboutmyop.org. This will not only allow patients to complete quality of life (PROMs) questionnaires online, but will also allow them to access information on their condition and necessary surgery, in addition to post-operative follow-up.
Detailed Description
Patients referred with gallstone disease necessitating surgery (laparoscopic cholecystectomy) will be invited to engage with our on-line interactive website. This will allow a two-way exchange of information in a secure environment (N3 compliant) to inform the patient about the risks, benefits, alternatives to surgery (cholecystectomy), and post- operative expectations. Furthermore, it will inform clinicians about the patient's symptoms and history, and record a pre-operative Patient Reported Outcome Measure (PROM). The patient's understanding of the facts required for informed consent will be measured and a "Patient Health & Understanding Report" generated for hospital clinicians. This will form part of the electronic patient record, and will be a medico-legal document. As with current practice patients will still attend their initial outpatient clinic appointment where they will meet a surgeon who will determine the appropriateness of surgery. Informed consent for surgery (cholecystectomy) will be obtained at this initial consultation facilitated by the information obtained from the "Patient Health & Understanding Report". The patient will then continue to interact with the on-line platform before and after their operation to ensure they are well informed and to monitor their post-operative progress. 7 days after surgery the patient will be prompted to interact with the website to answer questions about their progress and recovery. This will replace the existing telephone follow-up interaction. Any problems identified will trigger a protocol driven interaction between the hospital and the patient. At 1, 3 and 6 months after surgery a post-operative PROMs questionnaire will be answered by the patient allowing comparison of pre- and post-operative PROMs. This study will lead to the largest PROMs assessment of the effectiveness of laparoscopic cholecystectomy, will study the feasibility of our Website as a multimedia application in assisting with the process of informed consent, and will determine whether telephone follow-up can be safely replaced by a protocol driven online system.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gallstone Disease
Keywords
laparoscopic cholecystectomy

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
349 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Open Label
Arm Type
Other
Arm Description
Administration of a disease-specific and generic PROMs survey to patients undergoing Laparoscopic Cholecystectomy
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic cholecystectomy
Intervention Description
Administration of a disease-specific and generic PROMs survey to patients undergoing Laparoscopic Cholecystectomy
Primary Outcome Measure Information:
Title
Mean domain PROMs scores for each study participant
Description
We will look at the change in score between: pre--op and 30-Days, Pre-op and 3 Months post-op and pre-op and 6 months post-op. For this analysis we hope to use the paired t---test, however depending on whether the data is normally distributed or not this may require non---parametric analyses with the Wilcoxon rank---sum test. We also aim to look at the overall trend, which will require analysis of variance.
Time Frame
30-Days,3 Months and 6 Months
Secondary Outcome Measure Information:
Title
Completion of the Multimedia Informed Consent package on aboutmyop.org
Time Frame
30 days
Title
Completion of the 7---Day follow---up questionnaire.
Time Frame
7 days
Title
Completion of a Patient Satisfaction Survey to receive feedback on the process.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female. Adults:aged 18 to 85 years. Be referred for consideration for an elective laparoscopic cholecystectomy for symptomatic gallstones based on their GPs diagnosis and referral to a general surgeon. Patients initially listed for laparoscopic cholecystectomy but subsequently converted to open cholecystectomy or subsequently have a more complex 'biliary' procedure (including but not exclusive to bile duct exploration, biliary drain insertion, biliary bypass procedure). Exclusion Criteria: Patients unable to, or those choosing not to engage with the multimedia process --- including patients lacking mental capacity, patients who do not have access to a multimedia device (including but not exclusive to a computer, tablet or multimedia phone), patients who are unable to use a multimedia device unassisted. Patients who are unable to read or communicate n English without the presence of a translator. Patients undergoing another major non---biliary operation during the same operation as their cholecystectomy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prita Daliya, MBChB, MRCS, PGDip(Hons)
Organizational Affiliation
Nottingham University Hospitals NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nottingham University Hospitals NHS Trust
City
Nottingham
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35953737
Citation
Daliya P, Carvell J, Rozentals J, Lobo DN, Parsons SL. Digital Follow-Up After Elective Laparoscopic Cholecystectomy: A Feasibility Study. World J Surg. 2022 Nov;46(11):2648-2658. doi: 10.1007/s00268-022-06684-w. Epub 2022 Aug 11.
Results Reference
derived

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Multimedia Informed Consent & PROMs in Laparoscopic Cholecystectomy

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