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Comprehensive Optimization At-time of Radical Cystectomy Intervention (COARC)

Primary Purpose

Bladder Cancer, Radical Cystectomy

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Preop Intervention and Monitored Recovery
Usual Care
Sponsored by
University of Texas Southwestern Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Bladder Cancer focused on measuring Peri-operative

Eligibility Criteria

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

Inclusion Criteria: Adults equal to or more than 18 years old Diagnosis of bladder cancer with plan to undergo radical cystectomy Agrees to participate in study procedures Exclusion Criteria: Patients undergoing cystectomy for diagnosis other than bladder cancer Do not provide informed consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Intervention Arm

    Control Arm

    Arm Description

    Preop intervention Arm Referral to Perioperative Optimization of Senior Health (POSH) Program Remote patient monitoring device orientation, initial intake, and education UTSW ERAS protocol perioperatively Inpatient geriatrics co-management Monitored recovery Post-operative monitoring with Acticare for 90 days Post-op specialist continuity of care

    Enhanced Recovery After Surgery Usual referral and recovery care as needed Standard follow-up protocol

    Outcomes

    Primary Outcome Measures

    90 day complication rate
    Number of occurrences of complications at 90 days in patients in post-operative phase

    Secondary Outcome Measures

    30 day complication rate
    Number of occurrences of complications at 30 days in patients in post-operative phase
    Readmission rates
    Number of readmissions
    Adherence to the intervention
    It is assessed via patient-self report measure
    Changes in functional fitness as measured by step count
    Changes in functional fitness will be measured by step count
    QOL changes as measured by the Bladder Cancer Index and FACT-Bl-Cys Questionnaire measures
    Changes in patient reported outcomes will be measured by QOL (Bladder Cancer Index questionnaire). Possible scores range from 0-100, where higher scores indicate better HRQOL outcome. Changes will also be measured using the FACT-Bl-Cys tool to assess changes in bladder related quality of life in patients undergoing cystectomy over the course of the study.

    Full Information

    First Posted
    January 26, 2023
    Last Updated
    September 23, 2023
    Sponsor
    University of Texas Southwestern Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05714826
    Brief Title
    Comprehensive Optimization At-time of Radical Cystectomy Intervention
    Acronym
    COARC
    Official Title
    Comprehensive Optimization At-time of Radical Cystectomy Intervention Through Peri-operative Patient Care Program
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    December 20, 2023 (Anticipated)
    Primary Completion Date
    May 25, 2026 (Anticipated)
    Study Completion Date
    August 24, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Texas Southwestern Medical Center

    4. Oversight

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

    5. Study Description

    Brief Summary
    The proposed study is aimed at a comprehensive optimization at-time of radical cystectomy (COARC) intervention that focuses on patient optimization throughout the perioperative continuum, from the pre-operative setting to the post-operative period, among patients undergoing radical cystectomy for bladder cancer. This multi-modal strategy will focus on three phases of care around surgery: the pre-operative, peri-operative, and post-operative phases. The intervention group will focus on multiple areas of patient optimization including remote patient monitoring for the earlier identification of potential complications. The overall study mission is to decrease complication rates after radical cystectomy using this comprehensive approach.
    Detailed Description
    The proposed study includes the following- Part I: Pre-operative period After randomization, patients in the intervention group will be referred to the Perioperative Optimization of Senior Health (POSH) program where they will undergo nutritional, functional, and global health assessment. The POSH team will refer patients as indicated to nutrition, physical medicine and rehabilitation, and other consultants to optimize their preoperative fitness for surgery. Patients in the intervention group will also receive a Remote Patient Monitoring (RPM) Ipad from ActiCare Health, which will serve as their remote monitoring device and educational tool. At enrollment, they will be asked to complete an initial steps intake using a pedometer that will be provided to them. They will be asked to input vital signs once per week after receiving the Ipad to become familiar with the platform pre-operatively. At enrollment, patients in both groups will also be asked to complete a patient reported Bladder Cancer Index questionnaire, a survey that tracks quality of life in patients with bladder cancer. Part II: Perioperative period Both the intervention and control groups will undergo standard of care Enhanced Recover After Surgery (ERAS) bladder cancer protocol, which is a medication and peri-operative management protocol developed by the anesthesia and urology departments specifically for bladder cancer patients undergoing radical cystectomy. While admitted in the hospital recovering from surgery, patients in the intervention group will automatically receive co-management from the POSH team. Part III: Post-operative period Both the intervention and the control groups will be followed for 90 days post-operatively. The intervention group will use the RPM Ipad to input vital signs, weight, and pedometer steps 3x/week and on an as needed basis over the follow-up period which will be monitored by the ActiCare Health 24/7 clinical support team. Abnormal parameters will be set so that the UT Southwestern Medical Center clinical care team is alerted to any abnormal values.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Bladder Cancer, Radical Cystectomy
    Keywords
    Peri-operative

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    It is a prospective randomized study that implements a multi-modal digitally based comprehensive health optimization program in the pre and post-operative setting in patients undergoing radical cystectomy for muscle invasive bladder cancer. Two patient groups will be enrolled and randomized where one group will go through the peri-operative optimization programs and the other group will receive the usual pre-op care followed by post-op care via standard follow-up protocol.
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    194 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention Arm
    Arm Type
    Experimental
    Arm Description
    Preop intervention Arm Referral to Perioperative Optimization of Senior Health (POSH) Program Remote patient monitoring device orientation, initial intake, and education UTSW ERAS protocol perioperatively Inpatient geriatrics co-management Monitored recovery Post-operative monitoring with Acticare for 90 days Post-op specialist continuity of care
    Arm Title
    Control Arm
    Arm Type
    Active Comparator
    Arm Description
    Enhanced Recovery After Surgery Usual referral and recovery care as needed Standard follow-up protocol
    Intervention Type
    Other
    Intervention Name(s)
    Preop Intervention and Monitored Recovery
    Other Intervention Name(s)
    Monitored recovery during post-operative phase
    Intervention Description
    Perioperative Optimization of Senior Health (POSH) Program; patient monitoring by device orientation, initial intake, education; ERAS protocol, inpatient geriatric co-management; and remote monitoring with Acticare device; post-op continuity of care
    Intervention Type
    Other
    Intervention Name(s)
    Usual Care
    Intervention Description
    ERAS, Usual referral and recovery care, and Standard follow-up protocol
    Primary Outcome Measure Information:
    Title
    90 day complication rate
    Description
    Number of occurrences of complications at 90 days in patients in post-operative phase
    Time Frame
    90 days
    Secondary Outcome Measure Information:
    Title
    30 day complication rate
    Description
    Number of occurrences of complications at 30 days in patients in post-operative phase
    Time Frame
    30 days
    Title
    Readmission rates
    Description
    Number of readmissions
    Time Frame
    90 days
    Title
    Adherence to the intervention
    Description
    It is assessed via patient-self report measure
    Time Frame
    90 days
    Title
    Changes in functional fitness as measured by step count
    Description
    Changes in functional fitness will be measured by step count
    Time Frame
    Baseline, 90 days
    Title
    QOL changes as measured by the Bladder Cancer Index and FACT-Bl-Cys Questionnaire measures
    Description
    Changes in patient reported outcomes will be measured by QOL (Bladder Cancer Index questionnaire). Possible scores range from 0-100, where higher scores indicate better HRQOL outcome. Changes will also be measured using the FACT-Bl-Cys tool to assess changes in bladder related quality of life in patients undergoing cystectomy over the course of the study.
    Time Frame
    Baseline, 90 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Adults equal to or more than 18 years old Diagnosis of bladder cancer with plan to undergo radical cystectomy Agrees to participate in study procedures Exclusion Criteria: Patients undergoing cystectomy for diagnosis other than bladder cancer Do not provide informed consent
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jacob Taylor, MD, MPH
    Phone
    781-789-7047
    Email
    Jacob.Taylor@UTSouthwestern.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Yair Lotan, MD
    Organizational Affiliation
    UT Southwestern Medical Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Comprehensive Optimization At-time of Radical Cystectomy Intervention

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