RECRUITING

Harm Reduction Services

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 purpose of this study is to assess whether an integrated harm reduction intervention (IHRI), compared to harm reduction (HR) services as usual, will improve harm reduction service utilization among Black and Latinx people who use drugs (PWUD).

Official Title

Culturally Response Integrated Harm Reduction Services for Black and Latinx People Who Use Drugs

Quick Facts

Study Start:2024-11-26
Study Completion:2028-03-28
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05776316

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. * at least 18 years of age
  2. * self-identified as misusing opioids +/- other substances (stimulants) in the past 30 days, confirmed by interview using DSM-5 criteria
  3. * English or Spanish speaking
  4. * able to provide informed consent.
  1. * inability to provide informed consent or participate in the study procedures as proposed in the consent
  2. * active suicidal or homicidal ideation or an unstable psychotic disorder (schizophrenia, schizoaffective disorder) or mood disorder (bipolar disorder, severe major depressive disorder)
  3. * an unwillingness to be randomized.
  4. * are prisoners

Contacts and Locations

Study Contact

Ayana Jordan, MD, PhD
CONTACT
646-754-4858
Ayana.Jordan@nyulangone.org

Principal Investigator

Ayana Jordan, MD, PhD
PRINCIPAL_INVESTIGATOR
NYU Langone Health

Study Locations (Sites)

Yale University
New Haven, Connecticut, 06520
United States
NYU Langone Health
New York, New York, 10016
United States
Nathan Kline Institute
Orangeburg, New York, 10962
United States

Collaborators and Investigators

Sponsor: NYU Langone Health

  • Ayana Jordan, MD, PhD, PRINCIPAL_INVESTIGATOR, NYU Langone Health

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 Date2024-11-26
Study Completion Date2028-03-28

Study Record Updates

Study Start Date2024-11-26
Study Completion Date2028-03-28

Terms related to this study

Keywords Provided by Researchers

  • Harm Reduction
  • Latinx/Hispanix
  • Black/African American
  • Drug Use
  • Cocaine
  • Opioids
  • Methamphetamines

Additional Relevant MeSH Terms

  • Drug Use
  • Substance Abuse
  • Mental Illness