RECRUITING

Impact of 4PCP on Practitioner and Patient Outcomes

Conditions

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

Reducing opioid prescribing and improving outcomes in patients with chronic pain would benefit our nation. Neither addiction nor chronic pain spares any race, gender, or particular socio-economic status. This study is investigating a potentially inexpensive way of providing a previously costly service (the intensive chronic pain rehabilitation program), which is why insurers stopped covering it. Although it is unusual for an application from an academic institution to include a startup company (PainSTakers, LLC) as the curriculum provider, this is actually a long-term strength of this program, and the reason NIH recommended this route. It ensures that 4PCP will ultimately sustain itself rather than require government support for its continuation. Support for this application is not to provide the curriculum, but to determine if it is effective in the outcomes expected to be found. The curriculum is being provided freely only as an incentive for practitioners to participate in the research portion of the study. If the study is able to demonstrate its clinical effectiveness, the next step will be to show a positive economic impact for health care institutions and for health insurers who may then wish to support the program for their practitioners and their patients.

Official Title

Impact of a Novel Community-Based Biobehavioral Chronic Pain Team Training Program (4PCP) on Practitioner and Patient Outcomes

Quick Facts

Study Start:2023-03-17
Study Completion:2027-10
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05580419

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:14 Years to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, 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

Study Contact

Thomas Chelimsky, M.D.
CONTACT
(804)-628-0145
thomas.chelimsky@vcuhealth.org
Madison Maxwell, B.S.
CONTACT
madison.maxwell@vcuhealth.org

Principal Investigator

Thomas Chelimsky, M.D.
PRINCIPAL_INVESTIGATOR
VCU

Study Locations (Sites)

Case Western Reserve University
Cleveland, Ohio, 44106
United States
Virginia Commonwealth University
Richmond, Virginia, 23298
United States
Wisconsin Research and Education Network (WREN)
Madison, Wisconsin, 53715
United States
SSM Health
Madison, Wisconsin, 53716
United States

Collaborators and Investigators

Sponsor: Virginia Commonwealth University

  • Thomas Chelimsky, M.D., PRINCIPAL_INVESTIGATOR, VCU

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 Date2023-03-17
Study Completion Date2027-10

Study Record Updates

Study Start Date2023-03-17
Study Completion Date2027-10

Terms related to this study

Additional Relevant MeSH Terms

  • Chronic Pain