RECRUITING

Comprehensive Optimization At-time of Radical Cystectomy Intervention

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Comprehensive Optimization At-time of Radical Cystectomy Intervention Through Peri-operative Patient Care Program

Quick Facts

Study Start:2024-04-25
Study Completion:2026-08-24
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05714826

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adults equal to or more than 18 years old
  2. * Diagnosis of bladder cancer with plan to undergo radical cystectomy
  3. * Agrees to participate in study procedures
  1. * Patients undergoing cystectomy for diagnosis other than bladder cancer
  2. * Do not provide informed consent

Contacts and Locations

Study Contact

Jacob Taylor, MD, MPH
CONTACT
781-789-7047
Jacob.Taylor@UTSouthwestern.edu

Principal Investigator

Yair Lotan, MD
PRINCIPAL_INVESTIGATOR
UT Southwestern Medical Center

Study Locations (Sites)

University of Texas Southwestern Medical Center
Dallas, Texas, 75390-9164
United States

Collaborators and Investigators

Sponsor: University of Texas Southwestern Medical Center

  • Yair Lotan, MD, PRINCIPAL_INVESTIGATOR, UT Southwestern Medical Center

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 Registration Dates

Study Start Date2024-04-25
Study Completion Date2026-08-24

Study Record Updates

Study Start Date2024-04-25
Study Completion Date2026-08-24

Terms related to this study

Keywords Provided by Researchers

  • Peri-operative

Additional Relevant MeSH Terms

  • Bladder Cancer
  • Radical Cystectomy