COMPLETED

Recommendations of Enhanced Recovery Interventions for Patient's Clinical Team and Collection of Associated Data

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

This REMAP Periop ERP domain study falls under the Periop Core Protocol, which compares the different recommended strategies for enhancing recovery through the use of various standard of care treatments before, during and after surgery in all patients with elective surgical encounters at UPMC who meet eligibility criteria. The ERP domain seeks to enhance recovery by optimizing strategies of perioperative care through evaluating combinations of perioperative treatment, which consists of preoperative, intraoperative and postoperative care. Optimal combinations of perioperative care will be generated and analyzed to determine the best outcomes for patients as defined by reduction in hospital free days, reduction in postoperative nausea and vomiting, and improved pain control.

Official Title

Randomized, Embedded, Multifactorial Adaptive Platform for Perioperative Medicine at UPMC (UPMC REMAP): Core Protocol - Enhanced Recovery Protocols (ERP)

Quick Facts

Study Start:2023-05-15
Study Completion:2025-03-21
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT04606264

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. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Principal Investigator

Stephen Esper, MD, MBA
STUDY_CHAIR
University of Pittsburgh

Study Locations (Sites)

UPMC Magee-Womens Hospital
Pittsburgh, Pennsylvania, 15213
United States
UPMC Presbyterian
Pittsburgh, Pennsylvania, 15213
United States
UPMC Passavant
Pittsburgh, Pennsylvania, 15237
United States

Collaborators and Investigators

Sponsor: Jennifer Holder-Murray

  • Stephen Esper, MD, MBA, STUDY_CHAIR, University of Pittsburgh

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 Date2023-05-15
Study Completion Date2025-03-21

Study Record Updates

Study Start Date2023-05-15
Study Completion Date2025-03-21

Terms related to this study

Keywords Provided by Researchers

  • perioperative
  • enhanced recovery
  • patient-directed care
  • randomized embedded multifactorial adaptive platform
  • REMAP
  • ERP
  • 90-day hospital free days
  • length of stay
  • perioperative optimization
  • oral morphine equivalents
  • postoperative nausea and vomiting
  • readmission

Additional Relevant MeSH Terms

  • Perioperative Optimization