- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01237691
An Evaluation of California's Experiment With HOPE
April 6, 2018 updated by: Pepperdine University
Phase 1 Study of California's HOPE Experiment
The phase I evaluation is intended to assess whether or not frequent drug testing and immediate short-term incarceration for drug use and/or other violations and mandated drug treatment for multiple violations, reduces the recurrence of drug use and/or other violation behaviors by California parolees assigned to the study group.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The California HOPE pilot program is being implemented under the authority granted in Penal Code 5058.1.
The phase I evaluation is intended to assess whether or not frequent drug testing and immediate short-term incarceration for drug use and/or other violations and mandated drug treatment for multiple violations, reduces the recurrence of drug use and/or other violation behaviors by California parolees assigned to the study group compared with parole-as-usual.
Study Type
Interventional
Enrollment (Anticipated)
105
Phase
- Not Applicable
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
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Sacramento, California, United States, 95811
- Sacramento Metro IV Parole Unit.
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Assigned to the Sacramento Metro IV Parole Unit.
- Released from a term of return-to-custody for a violation for, or involving, the use of drugs.
- Have a maximum controlling discharge date at least one year from the date of release from the return-to-custody term.
Exclusion Criteria:
- History of convictions for crimes that require registration under Penal Code Section 290.
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
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: HOPE supervision
Parolee supervised under California's new HOPE parole model.
|
HOPE entails a warning session (Orientation Hearing) where the rules of parole are laid out and parolees are told that any violation of stated parole conditions will be sanctioned with a brief jail term (typically a few days in jail).
HOPE includes regular random drug testing.
Other Names:
|
Active Comparator: Parole-as-usual
Parolees supervised under California parole-as-usual.
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Parolees are supervised under standard parole supervision practice in California.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Days incarcerated
Time Frame: 24 months
|
Total number of days incarcerated in jail or prison
|
24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
% positive drug tests
Time Frame: 24 months
|
Percentage of random and scheduled drug tests that test positive for illicit drugs
|
24 months
|
%Missed
Time Frame: 24 months
|
Percentage of parole appointments that are missed.
|
24 months
|
Revocation rate
Time Frame: 24 months
|
Percentage of parolees that are revoked from probation and returned to prison for either a technical violation or on a new charge.
|
24 months
|
New arrests
Time Frame: 24 months
|
Number of new arrests.
|
24 months
|
Perceptions of risk of detection
Time Frame: 24 months
|
Parolees perceived risk of detection for drug use
|
24 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
November 1, 2010
Primary Completion (Actual)
October 1, 2012
Study Completion (Actual)
March 1, 2013
Study Registration Dates
First Submitted
November 1, 2010
First Submitted That Met QC Criteria
November 8, 2010
First Posted (Estimate)
November 9, 2010
Study Record Updates
Last Update Posted (Actual)
April 10, 2018
Last Update Submitted That Met QC Criteria
April 6, 2018
Last Verified
April 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- SPPN1110F01
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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