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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
United States
Texas
University of Texas Southwestern Medical Center
RECRUITING
Dallas
Contact Information
Primary
Jacob Taylor, MD, MPH
Jacob.Taylor@UTSouthwestern.edu
781-789-7047
Time Frame
Start Date: 2024-04-25
Estimated Completion Date: 2026-08-24
Participants
Target number of participants: 194
Treatments
Experimental: Intervention Arm
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
Active_comparator: Control Arm
Enhanced Recovery After Surgery Usual referral and recovery care as needed Standard follow-up protocol
Related Therapeutic Areas
Sponsors
Leads: University of Texas Southwestern Medical Center

This content was sourced from clinicaltrials.gov