RECRUITING

PRECISION Pain Research Registry

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 PRECISION Pain Research Registry enrolls participants with chronic low back pain (cases) and participants who are free of chronic pain (controls) to study the epidemiology and management of chronic pain. The vision of the registry is to conduct research to provide a future for all unbounded by pain.

Official Title

Pain Registry for Epidemiological, Clinical, and Interventional Studies and Innovation

Quick Facts

Study Start:2016-04
Study Completion:2030-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04853732

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:21 Years to 79 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Must reside within the contiguous 48 United States or District of Columbia
  2. * Must provide a valid, government-issued identification with photo and birthdate
  3. * Must have Internet access or telephone service to communicate with registry staff
  4. * Must have sufficient English language proficiency to complete case report forms independently or with assistance from registry staff
  5. * Must have a primary care physician or other physician who regularly provides health care
  6. * Must provide the name, dose, and frequency of use of all current medications
  7. * Case participants must have chronic low back pain
  8. * Control participants must be free of any chronic pain and may include healthy volunteers
  1. * Must not be pregnant
  2. * Must not reside in an institutional facility

Contacts and Locations

Study Contact

Cathleen Kearns, BA
CONTACT
817-735-0515
orcstudyoperations@unthsc.edu
Samantha Johnson, BS
CONTACT
817-735-5410
orcstudyoperations@unthsc.edu

Principal Investigator

John C Licciardone, DO, MS, MBA
PRINCIPAL_INVESTIGATOR
University of North Texas Health Science Center

Study Locations (Sites)

University of North Texas Health Science Center
Fort Worth, Texas, 76107
United States

Collaborators and Investigators

Sponsor: University of North Texas Health Science Center

  • John C Licciardone, DO, MS, MBA, PRINCIPAL_INVESTIGATOR, University of North Texas Health Science Center

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 Date2016-04
Study Completion Date2030-12

Study Record Updates

Study Start Date2016-04
Study Completion Date2030-12

Terms related to this study

Additional Relevant MeSH Terms

  • Chronic Low Back Pain