- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03102151
Reducing the Duration of Untreated Psychosis (ReduceDUP)
January 10, 2023 updated by: Steven R. Lopez, University of Southern California
Reducing the Duration of Untreated Psychosis Through Community Education
The study examines the possible effect of a community campaign to decrease the duration of untreated psychosis in persons with their first episode of a psychotic disorder.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study examines whether a community campaign can reduce over time the duration of untreated psychosis (DUP) among persons with first episode psychosis (FEP).
The DUP of mental health patients with FEP who sought services at a public outpatient or an inpatient facility was assessed for a 15 month period prior to the campaign launch.
This serves as the baseline or historical control.
The DUP will continue to be assessed for another 3 years.
The hypothesis being tested is that there will be a significant decrease in DUP between baseline, one-year, two-year and three-year follow-ups.
This study is being carried out with Latinos in Los Angeles County because as a group, particularly among Spanish-speaking immigrants, Latinos are at high risk for prolonged DUP.
Study Type
Observational
Enrollment (Actual)
137
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Granada Hills, California, United States, 91344
- San Fernando Mental Health Center
-
-
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.
Eligibility Criteria
Ages Eligible for Study
15 years to 65 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Living in the catchment area of San Fernando Mental Health Outpatient clinic, a clinic with the Los Angeles County Department of Mental Health
Description
Inclusion Criteria:
- Meet Diagnostic and Statistical Manual-4 criteria for a psychotic disorder
- of Latino origin
Exclusion Criteria:
- has a neurological disorder or suffers from brain trauma
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Ecologic or Community
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Latency to Treatment (LTT) a novel interview based assessment tool to measure the Duration of Untreated Psychosis
Time Frame: At the time of recruitment into the study
|
The time from the onset of psychosis to the time the subject receives appropriate mental health treatment.
The metric is number of weeks that the person went without treatment from illness onset.
The number of weeks is the variable of interest that will be aggregated.
|
At the time of recruitment into the study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Psychosis literacy, a questionnaire based inquiry for which the respondents answer either open-ended questions (e.g., What is serious mental Illness?) or "Yes-no" questions ("e.g., Can you recognize a serious mental illness in others?)
Time Frame: At the time of recruitment in to study
|
The responses to the interview are either written down or audio-recorded.
Raters then listen or read the responses and code them.
The responses are aggregated as frequencies (e.g., the number of symptoms identified) or as percentages (e.g., the proportion of respondents who reported that they can recognize a serious mental illness in others).
|
At the time of recruitment in to study
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Steven Lopez, PhD, University of Southern California
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 Major Dates
Study Start (Actual)
May 1, 2014
Primary Completion (Actual)
December 31, 2018
Study Completion (Actual)
August 30, 2019
Study Registration Dates
First Submitted
August 1, 2016
First Submitted That Met QC Criteria
March 29, 2017
First Posted (Actual)
April 5, 2017
Study Record Updates
Last Update Posted (Estimate)
January 11, 2023
Last Update Submitted That Met QC Criteria
January 10, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- USCLaCLAVE
- 1R01MH103830 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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