TERMINATED

Standard Care Coordination Expansion Pilot

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 Standard Care Coordination (SCC) solution integrates aspects of case management \& care coordination \& was designed by UnitedHealth Group for high-cost, complex, at-risk consumers to facilitate health care access and decisions that can have a dramatic impact on the quality and affordability of the consumer's health care. Currently members only receive the SCC if they are: 1) identified as high risk for readmission upon discharge from the hospital, 2) are self-referred, or 3) are directly referred to the program by their physician. The current quality improvement study was designed as a randomized controlled trial to determine if the expansion of the SCC program to commercially insured members identified via a proprietary administrative algorithms as being at high risk would significantly impact rates of acute inpatient admissions.

Official Title

Standard Care Coordination Expansion Pilot - A Quality Improvement Study

Quick Facts

Study Start:2015-10
Study Completion:2023-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:TERMINATED

Study ID

NCT04415515

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. * UnitedHealthcare commercial Fully Insured members; all states; 18+ years old; actively enrolled in the health plan as of randomization identified via proprietary administrative algorithm as being at high risk for persistent super utilizer status.
  1. * : pregnant women, individuals prescribed medications for infertility, members with evidence of dementing disorders, members indicated as "do not contact " for program outreach, and Members in the following products and plans:
  2. * legacy UHC ASO groups (populations for which UHC provides administrative services only),
  3. * legacy Oxford health plan members (all members receive the SCC program),
  4. * legacy PacifiCare members,
  5. * legacy River Valley/NHP members, and
  6. * Public Sector clients
  7. * the PHS 2.0 intervention (a small population within Fully Insured)
  8. * assignment to a clinically activated Accountable Care Organization (ACO)

Contacts and Locations

Principal Investigator

Anthony V Pirrello, MS
PRINCIPAL_INVESTIGATOR
UnitedHealthcare

Study Locations (Sites)

UnitedHealthcare
Minnetonka, Minnesota, 55343
United States

Collaborators and Investigators

Sponsor: UnitedHealthcare

  • Anthony V Pirrello, MS, PRINCIPAL_INVESTIGATOR, UnitedHealthcare

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 Date2015-10
Study Completion Date2023-12

Study Record Updates

Study Start Date2015-10
Study Completion Date2023-12

Terms related to this study

Keywords Provided by Researchers

  • Care coordination, case management, superutilizers, health care utilization

Additional Relevant MeSH Terms

  • Superutilizers, Health Care Utilization