Evaluation of Image-Based Modelling on Clinical Decisions in Coarctation of the Aorta
Primary Purpose
Congenital Heart Disease, Aortic Coarctation, Cardiovascular Disease
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Image-based simulation modelling
Imaging parameters currently recommended by clinical practice guidelines
Sponsored by
About this trial
This is an interventional health services research trial for Congenital Heart Disease focused on measuring cardiovascular modeling, aortic coarctation, virtual stenting
Eligibility Criteria
Inclusion Criteria:
- Practicing interventional cardiologists
- Has treated patients with coarctation of the aorta during the past 6 months
Exclusion Criteria:
- Participation in CARDIOPROOF trial
Sites / Locations
- London School of Economics and Political Science
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Group A
Group B
Arm Description
Interventional cardiologists presented with "limited" dataset including only information that is available from imaging parameters currently recommended by clinical practice guidelines.
Interventional cardiologists presented with the full dataset, including imaging parameters currently recommended by clinical practice guidelines and image-based simulation modelling.
Outcomes
Primary Outcome Measures
Decision to intervene
Our primary outcome of interest in this randomized experiment will be 'decision to intervene' by cardiologists evaluating imaging data obtained from patients with aortic coarctation. Interventional cardiologists will be asked the following question:
Based on the information presented to you, would you intervene in this patient now? Please provide a yes/no answer.
Secondary Outcome Measures
Full Information
NCT ID
NCT02700737
First Posted
December 11, 2015
Last Updated
October 28, 2016
Sponsor
London School of Economics and Political Science
Collaborators
German Heart Institute, Bambino Gesù Hospital and Research Institute, University College, London
1. Study Identification
Unique Protocol Identification Number
NCT02700737
Brief Title
Evaluation of Image-Based Modelling on Clinical Decisions in Coarctation of the Aorta
Official Title
Evaluation of Image-Based Modelling on Clinical Decisions in Coarctation of the Aorta
Study Type
Interventional
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
May 2016 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
August 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
London School of Economics and Political Science
Collaborators
German Heart Institute, Bambino Gesù Hospital and Research Institute, University College, London
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
To answer the research question: "Would image-based modelling result in different clinical decisions as compared to clinical practice guidelines?", we will conduct a randomized controlled experiment in which we will compare the hypothetical decisions made by interventional cardiologists who are presented with imaging parameters currently recommended by clinical practice guidelines vs. hypothetical decisions made by interventional cardiologists receiving an expanded list of parameters, including simulation modelling.
Detailed Description
In collaboration with our three clinical partners, we will first generate two separate imaging datasets for a maximum of three patients recruited to participate in CARDIOPROOF. The first dataset will include the imaging parameters currently recommended by clinical practice guidelines (referred to as "limited dataset"). The second dataset will include an expanded list of parameters, inclusive of information that is available from traditional imaging parameters (as recommended by the guidelines) and simulation modeling (referred to as "image-based modelling dataset").
We will generate both limited and image-based modelling datasets from fully de-identified patients already enrolled in CARDIOPROOF (NCT02591940) who have consented to publication of data in anonymized form.
Using a computerized random-sample function, we will randomly allocate interventional cardiologists into two separate groups and present them with one set of imaging data. The first group will receive a "limited" dataset including only information that is available from traditional diagnostics (as recommended by the clinical practice guidelines) for a pre-specified number of patients (maximum of 3). The second group will receive the full, detailed dataset inclusive of information that is available from traditional diagnostics (as recommended by the guidelines) and simulation modelling for the same set of patients.
We will then ask the interventional cardiologists in the two groups to make (hypothetical) clinical decisions using the dataset of imaging parameters presented to them. The clinical decisions will be hypothetical because patients will have been treated according to clinical practice guidelines and this experiment will retrospectively involve interventional cardiologists who are not directly involved in the care of the patients participating in CARDIOPROOF.
The analysis will focus on each hypothetical scenario and compare the proportions of cardiologists making different types of intervention decisions in the two randomly allocated groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Disease, Aortic Coarctation, Cardiovascular Disease
Keywords
cardiovascular modeling, aortic coarctation, virtual stenting
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
206 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group A
Arm Type
Active Comparator
Arm Description
Interventional cardiologists presented with "limited" dataset including only information that is available from imaging parameters currently recommended by clinical practice guidelines.
Arm Title
Group B
Arm Type
Experimental
Arm Description
Interventional cardiologists presented with the full dataset, including imaging parameters currently recommended by clinical practice guidelines and image-based simulation modelling.
Intervention Type
Other
Intervention Name(s)
Image-based simulation modelling
Intervention Description
The first dataset will include the imaging parameters currently recommended by clinical practice guidelines (referred to as "limited dataset").
Intervention Type
Other
Intervention Name(s)
Imaging parameters currently recommended by clinical practice guidelines
Intervention Description
The second dataset will include an expanded list of parameters, inclusive of information that is available from traditional imaging parameters (as recommended by the guidelines) and simulation modeling (referred to as "image-based modelling dataset").
Primary Outcome Measure Information:
Title
Decision to intervene
Description
Our primary outcome of interest in this randomized experiment will be 'decision to intervene' by cardiologists evaluating imaging data obtained from patients with aortic coarctation. Interventional cardiologists will be asked the following question:
Based on the information presented to you, would you intervene in this patient now? Please provide a yes/no answer.
Time Frame
Immediate
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Practicing interventional cardiologists
Has treated patients with coarctation of the aorta during the past 6 months
Exclusion Criteria:
Participation in CARDIOPROOF trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Huseyin Naci, PhD
Organizational Affiliation
London School of Economics and Political Science
Official's Role
Principal Investigator
Facility Information:
Facility Name
London School of Economics and Political Science
City
London
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
31304365
Citation
Naci H, Salcher-Konrad M, Mcguire A, Berger F, Kuehne T, Goubergrits L, Muthurangu V, Wilson B, Kelm M. Impact of predictive medicine on therapeutic decision making: a randomized controlled trial in congenital heart disease. NPJ Digit Med. 2019 Mar 19;2:17. doi: 10.1038/s41746-019-0085-1. eCollection 2019.
Results Reference
derived
Links:
URL
http://www.cardioproof.eu
Description
Overall study website
Learn more about this trial
Evaluation of Image-Based Modelling on Clinical Decisions in Coarctation of the Aorta
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