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NCT04517279Completed

Peer Approaches to Substances in Early Psychosis Programs: A Pilot Study of a Peer-Led Intervention

Advancing the Early Psychosis Intervention Network in Texas

Source: ClinicalTrials.gov · Last updated 19 Dec 2025

Brief summary (registry, in English)

The aim of the study is to pilot a peer-provided, manualized intervention to increase the proportion of young people with first episode psychosis who reduce or stop substance use and improve psychiatric and functional outcomes. Coordinated specialty care teams will be randomly assigned to implement the intervention, Peer Approaches to Substances in Early Psychosis Programs (PAS-EPP), or usual care. The pilot study aims to: (a) determine if peer providers can implement PAS-EPP with adequate fidelity; (b) determine if youth and young adults engage in the intervention with peer providers and find it acceptable; (c) estimate the rates of drop-out for each of the two study arms; (d) estimate both between-participant (within-provider team) and between-team variability on key outcome measures; and (e) identify any changes needed to the intervention approach, manual, or training materials. The pilot study will set the stage for a future comparative cluster randomized trial of the intervention;

Status (registry)
Completed
Study type
Interventional
Enrollment
113 (actual)
First submitted
12 Aug 2020
Start date
22 Aug 2023
Primary completion date
25 Jul 2025
Lead sponsor
University of Texas at Austin
NCT number
NCT04517279

What you commit to

  • Study type: Interventional
  • Participants enrolled: 113
  • From 22 Aug 2023 to the primary completion date, 25 Jul 2025
  • 15 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • none

Who the study is looking for

  • enrolled in a CSC program during the defined study period;
  • continued program enrollment at six month follow-up from program entry;
  • continued alcohol/substance use at six-month follow-up from program entry.

Age in the registry: 15 years to 32 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (15)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Integral Care
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AustinUnited StatesUnknown status
Spindletop Centers
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BeaumontUnited StatesUnknown status
West Texas Centers
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Big SpringUnited StatesUnknown status
Metrocare Services
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DallasUnited StatesUnknown status
Denton County MHMR
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DentonUnited StatesUnknown status
The Harris Center for Mental Health and IDD
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HoustonUnited StatesUnknown status
Border Region Behavioral Health Center
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LaredoUnited StatesUnknown status
Community Healthcore
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LongviewUnited StatesUnknown status
Burke
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LufkinUnited StatesUnknown status
Coastal Plains
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PortlandUnited StatesUnknown status
Bluebonnet Trails Community Center
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Round RockUnited StatesUnknown status
Center for Healthcare Services
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San AntonioUnited StatesUnknown status
Central Counties Services
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TempleUnited StatesUnknown status
Andrews Behavioral Health
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TylerUnited StatesUnknown status
Pecan Valley Centers
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WeatherfordUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.