ACTIVE_NOT_RECRUITING

High-Risk Veteran Initiative

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

Veterans at high-risk for hospitalization, including those with complex care needs, represent a large population of VHA patients who often do not receive evidence-based primary care practices that would help them avoid the hospital and improve their health. The high-RIsk VETerans (RIVET) Program will implement evidence-based practices that can support VHA Primary Care teams to deliver more comprehensive and patient-centered care, better strategies to manage medications, and avoid unnecessary hospitalizations. The RIVET Program is designed to find the most effective approaches to increasing use of evidence-based practices for high-risk Veterans in primary care, provide rapid data feedback to VHA on high-risk patient care, build capacity for the implementation of evidence-based practices, and train future leaders in high-risk Veteran care.

Official Title

Improving Care for Complex, High-Risk Patients in Primary Care (QUE 20-018)

Quick Facts

Study Start:2021-07-23
Study Completion:2026-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05050643

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

Evelyn T Chang, MD MSHS
PRINCIPAL_INVESTIGATOR
VA Greater Los Angeles Healthcare System, Sepulveda, CA
Susan E Stockdale, PhD MA
PRINCIPAL_INVESTIGATOR
VA Greater Los Angeles Healthcare System, Sepulveda, CA

Study Locations (Sites)

VA Greater Los Angeles Healthcare System, Sepulveda, CA
Sepulveda, California, 91343
United States
VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
Pittsburgh, Pennsylvania, 15240
United States
VA Puget Sound Health Care System Seattle Division, Seattle, WA
Seattle, Washington, 98108-1532
United States

Collaborators and Investigators

Sponsor: VA Office of Research and Development

  • Evelyn T Chang, MD MSHS, PRINCIPAL_INVESTIGATOR, VA Greater Los Angeles Healthcare System, Sepulveda, CA
  • Susan E Stockdale, PhD MA, PRINCIPAL_INVESTIGATOR, VA Greater Los Angeles Healthcare System, Sepulveda, CA

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 Date2021-07-23
Study Completion Date2026-12-30

Study Record Updates

Study Start Date2021-07-23
Study Completion Date2026-12-30

Terms related to this study

Keywords Provided by Researchers

  • Primary Health Care
  • Multimorbidity
  • Medication Adherence
  • Needs Assessment
  • Mentoring

Additional Relevant MeSH Terms

  • Multimorbidity