- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04538677
Video Consultation During Follow up Surgical Care
September 3, 2020 updated by: Prof. dr. W.A. Bemelman, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Video Consultation During Follow up Care: Effect on Quality of Care and Patient- and Provider Attitude in Patients With Colorectal Cancer
The aim of this study was to compare the willingness to use and attitude towards VC amongst both patients with colorectal cancer and healthcare providers during follow up care.
Second, to determine the satisfaction with the quality of the healthcare provider and the usability of the used VC technology.
50 patients will be asked to choose between video consultation or face-to-face contact at the outpatient surgical clinic.
Study Overview
Study Type
Observational
Enrollment (Actual)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Amsterdam, Netherlands
- Amsterdam UMC, location AMC
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients with colorectal cancer scheduled for appointment at the surgical oncology outpatient a tertiary referral center.
Description
Inclusion Criteria:
- Age 18 years or older
- Fluent in speaking and writing in Dutch
- Follow up appointments in which overall progress, new complaints, results with good news and treatment was discussed were considered feasible.
Exclusion Criteria:
- Introductory appointments
- Bad news consultations
- Physical examination needed
- No access to Internet
- No access to a smartphone, tablet or computer with a camera
- Not willing to activate their electronic patient portal
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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F2F-Group
Patients who preferred a traditional F2F-appointment were seen at the outpatient clinic.
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VC-group
Patients who preferred a video consult were seen over a video connection.
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A two-way audio and visual connection between patients and surgeons
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Attitude and satisfaction with video consultation
Time Frame: Immediately after the consult
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PAT-VC questionnaire
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Immediately after the consult
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Usability of the video consultation technology
Time Frame: Immediately after the test consult
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SUS questionnaire
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Immediately after the test consult
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Quality of provided care by surgeon: MSF questionnaire
Time Frame: Immediately after the consult
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MSF questionnaire
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Immediately after the consult
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Satisfaction of surgeons: Questionnaire
Time Frame: Immediately after the consult
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Questionnaire
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Immediately after the consult
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2017
Primary Completion (Actual)
August 23, 2017
Study Completion (Actual)
August 23, 2017
Study Registration Dates
First Submitted
August 31, 2020
First Submitted That Met QC Criteria
September 3, 2020
First Posted (Actual)
September 4, 2020
Study Record Updates
Last Update Posted (Actual)
September 4, 2020
Last Update Submitted That Met QC Criteria
September 3, 2020
Last Verified
August 1, 2020
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- W17_149
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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