RECRUITING

Oklahoma Study of Native American Pain Risk III: Stress and Resilience

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 goal of this observational study is to learn about the relationship between environmental structural racism and discrimination and chronic pain risk in Native American adults. The main questions it aims to answer are: 1. How does environmental structural racism and discrimination affect chronic pain-promoting mechanisms in Native Americans? 2. What psychosocial factors buffer the negative effects of environmental structural racism and discrimination on chronic pain-promoting mechanisms?

Official Title

The Impact of Structural Racism and Discrimination (SRD) on Mechanisms of the Native American Pain Disparity

Quick Facts

Study Start:2023-02-03
Study Completion:2027-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05723081

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:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Self-identify as Native American/American Indian
  1. * \<18 years of age
  2. * Self-reported history of cardiovascular, neuroendocrine, musculoskeletal, or neurological disorders
  3. * Surrent chronic pain, defined as persistent, bothersome pain on more days than not for at least 3 months)
  4. * Self-reported current substance dependence
  5. * Sse of medication that could interfere with testing (e.g., recent use of analgesics, antidepressants, or anti-anxiety medications)
  6. * Inability to speak English
  7. * Current psychosis (assessed by Psychosis Screening Questionnaire)
  8. * Serious cognitive impairment (assessed by \<20 score on the Montreal Cognitive Assessment \[MoCA\])
  9. * Possible peripheral neuropathy (assessed by nerve conduction study)

Contacts and Locations

Study Contact

PLAN Lab
CONTACT
918-660-3048
tulsa.plan@gmail.com
Jamie L Rhudy, PhD
CONTACT
918-660-3050
jamie-rhudy@ouhsc.edu

Principal Investigator

Jamie L Rhudy, PhD
PRINCIPAL_INVESTIGATOR
University of Oklahoma

Study Locations (Sites)

University of Oklahoma - Schusterman Center
Tulsa, Oklahoma, 74135
United States

Collaborators and Investigators

Sponsor: University of Oklahoma

  • Jamie L Rhudy, PhD, PRINCIPAL_INVESTIGATOR, University of Oklahoma

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 Date2023-02-03
Study Completion Date2027-03-31

Study Record Updates

Study Start Date2023-02-03
Study Completion Date2027-03-31

Terms related to this study

Keywords Provided by Researchers

  • Structural racism and discrimination
  • Stress reactivity
  • Quantitative sensory testing

Additional Relevant MeSH Terms

  • Discrimination, Racial
  • Stress Physiology
  • Pain