RECRUITING

Peer to Peer (P2P): Mental Health Interventions with Persons with Substance Use Disorders

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

This study provides substance use and mental health peer support services to address behavioral health disparities in rural areas. Specifically, the project aims to address persistent mental health symptoms, such as anxiety and depression, that become barriers to care for patients working towards long-term recovery from co-occurring mental health and substance use disorders. Participants will be assessed and evaluated for opioid use disorder (OUD), social determinants of health (SDoH), and infectious diseases by a nurse practitioner and a social worker. A certified peer support specialist (CPSS) will provide additional support, connecting patients to sustainable mental health resources and implementing a modified version of the Friendship Bench intervention, which involves six weekly 45-minute problem-solving therapy sessions with the option to participate in six or more peer support sessions. The CPSS will follow the patient for up to 12 weeks.

Official Title

Peer to Peer (P2P): Mental Health Interventions with Persons with Substance Use Disorders

Quick Facts

Study Start:2024-11-11
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06803810

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. * Diagnosis of OUD via Diagnostic Statistical Manual (DSM)-V Text Revision (TR)
  2. * Receiving MOUD through the Mobile Recovery Program for at least 3 months
  3. * Age 18 or older
  4. * Moderate to Severe Depression with or without co-occurring anxiety as determined by PHQ-9 conducted during the most recent MRP clinical visit
  1. * Severe cognitive, medical, or psychiatric disability that could impair ability to perform study-related activities as determined by the MRP clinician or principal investigator.
  2. * Unable to read/speak English
  3. * Unable to read and comprehend the consent materials and other study materials
  4. * Current suicidal ideation based on the Patient Health Questionnaire-9

Contacts and Locations

Study Contact

Ashley King
CONTACT
704-936-9402
ashley.king3@prismahealth.org
Abby Blackwell
CONTACT
abigail.blackwell2@prismahealth.org

Principal Investigator

Alain Litwin
PRINCIPAL_INVESTIGATOR
Prisma Health

Study Locations (Sites)

Prisma Health
Greenville, South Carolina, 29605
United States

Collaborators and Investigators

Sponsor: Prisma Health-Upstate

  • Alain Litwin, PRINCIPAL_INVESTIGATOR, Prisma 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 Date2024-11-11
Study Completion Date2025-12

Study Record Updates

Study Start Date2024-11-11
Study Completion Date2025-12

Terms related to this study

Additional Relevant MeSH Terms

  • Standard of Care
  • P2P Intervention