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Improving Patient Reported Outcome Measures in Catheter Ablation

Primary Purpose

Ventricular Tachycardia, ICD, Quality of Life

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Validated quality of life questionnaire (EQ-5D & C-CAP)
Sponsored by
Barts & The London NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Ventricular Tachycardia focused on measuring Catheter ablation, Patient reported outcome measure, Incremental cost effectiveness ratio

Eligibility Criteria

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

Inclusion Criteria:

Adults (>18 years) With an Implantable Cardioverter Defibrillator (ICD) implanted >3 months from time of recruitment and a previous episode of documented VT requiring therapy from the ICD.

And impaired LV/RV function Willing and able to give written informed consent

Exclusion Criteria:

Patients who are planning to move away from study site within 12 months of enrolment who wished to use postal method to complete their HRQL Patients who are unable to give informed consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Intervention

    Comparator

    Arm Description

    Patients undergoing catheter ablation of VT

    Patients undergoing AAD therapy for VT

    Outcomes

    Primary Outcome Measures

    Completion rate of HRQL forms for patients undergoing VT ablation and those starting or continuing AAD therapy

    Secondary Outcome Measures

    Recruitment rate of patients who fulfil study criteria
    - Patient preferences for either paper or electronic HQRL (as a percentage of total recruitment)
    Patient reported HRQL of VT ablation and AAD therapy on both EQ-5D and C-CAP
    Impact on the cost-effectiveness calculation of VT ablation (using EQ-5D, and a number of different EQ-5D data points)
    Using the Incremental Cost-effectiveness ratio

    Full Information

    First Posted
    July 31, 2020
    Last Updated
    February 13, 2023
    Sponsor
    Barts & The London NHS Trust
    Collaborators
    University College, London
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04499326
    Brief Title
    Improving Patient Reported Outcome Measures in Catheter Ablation
    Official Title
    Use of Patient Reported Outcome Measures (PROMs) to Assess Quality of Life and Economic Evaluation of Cardiac Catheter Ablation of Ventricular Tachycardia: a Feasibility and Cohort Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    April 1, 2023 (Anticipated)
    Primary Completion Date
    October 1, 2024 (Anticipated)
    Study Completion Date
    October 1, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Barts & The London NHS Trust
    Collaborators
    University College, London

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This study will assess whether more frequent measurement of patient reported outcome measures (PROMs) - specifically health related quality of life (HRQL) - can improve the evaluation of the clinical effectiveness and cost-effectiveness of catheter ablation of ventricular tachycardia (VT) in patients with an Implantable Cardioverter Defibrillator (ICD). It is designed to have feasibility outcomes which contribute to answering the above.
    Detailed Description
    Patients who have been implanted with an ICD are at risk of suffering from dangerous arrhythmias such as VT. Patients can experience clinical events including worsening of any underlying heart failure regardless of either VT ablation or medical therapy treatment strategy (anti-arrhythmic drugs (AAD)). VT ablation is a specialist procedure which has been proven in randomised clinical trials (RCTs) to confer symptomatic relief from VT, reduced hospitalisations and reduced shocks from ICDs. However, there is no effect on mortality. The frequent nature of clinical events in this group of patients may affect their health status quite dramatically and yet based on current trial evidence, only 3 out of 6 randomised trials in VT ablation reported PROMs. This can lead to brittle conclusions about the overall cost-effectiveness profile of a procedure such as VT ablation. This study will assess for the feasibility of more frequent HRQL monitoring and its impact on whether it is able to better capture the clinical narrative and quality of life changes of patients with severe heart failure and an ICD. And thus the assessment of both clinical effectiveness and cost effectiveness of catheter ablation of VT or continuing anti arrhythmic drug therapy. METHOD & SETTING Single centre study at St Bartholomew's Hospital London. Patients will be identified through established local pathways - there are traditional outpatient specialist clinics where Consultant Cardiologists receive referrals of patients for consideration of managing patients with VT, including ablation. In addition, there are joint VT clinics operated by Consultants as well as by cardiac physiologists. In the outpatient VT clinic, 85 patients were seen in a 10-month window - it is assumed that this scale will allow feasible identification of patients to be recruited to the both the groups of this study.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Ventricular Tachycardia, ICD, Quality of Life
    Keywords
    Catheter ablation, Patient reported outcome measure, Incremental cost effectiveness ratio

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    70 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention
    Arm Type
    Experimental
    Arm Description
    Patients undergoing catheter ablation of VT
    Arm Title
    Comparator
    Arm Type
    Active Comparator
    Arm Description
    Patients undergoing AAD therapy for VT
    Intervention Type
    Other
    Intervention Name(s)
    Validated quality of life questionnaire (EQ-5D & C-CAP)
    Intervention Description
    Patient quality of life to be assessed at baseline, 1, 2, 3, 4, 6, 9 and 12 months
    Primary Outcome Measure Information:
    Title
    Completion rate of HRQL forms for patients undergoing VT ablation and those starting or continuing AAD therapy
    Time Frame
    1 year follow up
    Secondary Outcome Measure Information:
    Title
    Recruitment rate of patients who fulfil study criteria
    Time Frame
    1 year
    Title
    - Patient preferences for either paper or electronic HQRL (as a percentage of total recruitment)
    Time Frame
    1 year
    Title
    Patient reported HRQL of VT ablation and AAD therapy on both EQ-5D and C-CAP
    Time Frame
    18 months
    Title
    Impact on the cost-effectiveness calculation of VT ablation (using EQ-5D, and a number of different EQ-5D data points)
    Description
    Using the Incremental Cost-effectiveness ratio
    Time Frame
    18 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Adults (>18 years) With an Implantable Cardioverter Defibrillator (ICD) implanted >3 months from time of recruitment and a previous episode of documented VT requiring therapy from the ICD. And impaired LV/RV function Willing and able to give written informed consent Exclusion Criteria: Patients who are planning to move away from study site within 12 months of enrolment who wished to use postal method to complete their HRQL Patients who are unable to give informed consent
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Yang Chen, BM BCh
    Phone
    02034165000
    Email
    yang.chen@nhs.net
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Pier Lambiase, PhD
    Organizational Affiliation
    UCL
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    De-identified individual patient data for outcome measures will be made available
    IPD Sharing Time Frame
    In accordance with NHS Research governance framework
    IPD Sharing Access Criteria
    Upon reasonable request

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    Improving Patient Reported Outcome Measures in Catheter Ablation

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