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BehaviorNCT01343472

Evaluation of the Washington Intensive Supervision Program

A study testing WISP supervision and Parole-as-usual in people with Behavior and Drug Users, run by Pepperdine University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study entails an evaluation of the Washington Intensive Supervision Program (WISP). The purpose of the evaluation is to test whether subjects assigned to WISP perform better than those assigned to parole-as-usual (PAU). Read more about this study

Who is it for?
Ages 18 years and older, men only
Conditions the study is for
Behavior, Drug Users
What is being tested?
WISP supervision and Parole-as-usual
Could I receive a placebo?
No, everyone receives an active treatment
How many people
70 participants
Where
1 siteUnited States
Study dates
Jan 2011to Jun 2012
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Men only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Inmates released by DOC to community corrections supervision
  • Supervised out of the Seattle CJC (Community Justice Center) to include field offices and offenders from the downtown "Metro" unit, Southeast Seattle unit, Northgate (north Seattle) and West Seattle.
  • Have a parole supervision discharge date at least one year from the date of release from entry into WISP

Who cannot join

  • Level III Sex Offenders
  • Existing assignment to supervision that precludes WISP. These include: Drug Offender Sentencing Alternative (DOSA)and Special Sex Offender Sentencing Alternative (SSOSA).
  • Dangerously Mentally Ill (DMIO)

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Seattle Community Justice Center

    Seattle, Washington

Other trials in United States

About this study

This study entails an evaluation of the Washington Intensive Supervision Program (WISP). The purpose of the evaluation is to test whether subjects assigned to WISP perform better than those assigned to parole-as-usual (PAU).

Read the detailed description

This study entails an evaluation of the Washington Intensive Supervision Program (WISP). WISP is a program targeting high-risk parolees in Seattle, and is modeled after the HOPE program in Hawaii. The purpose of the evaluation is to test whether subjects assigned to WISP perform better than those assigned to parole-as-usual (PAU) on a number of outcomes, including drug use, missed appointments, recidivism, prison and jail stays, and parole revocations. WISP uses regular random drug testing and close community supervision, paired with swift and certain, but modest sanctions for every detected violation.

Conditions
Behavior, Drug Users
Being tested
WISP supervision, Parole-as-usual
Keywords
Behavior, Drug users
Medical subject headings
Behavior, Drug Misuse

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • WISP supervisionBehavioural

    Also called HOPE supervision

    WISP 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). WISP includes regular random drug testing.

  • Parole-as-usualBehavioural

    Also called PAU

    Parolees are supervised under standard parole supervision practice in Washington State.

Study groups in NCT01343472
Study groupRoleWhat they receive
WISP supervisionExperimentalParolee supervised under WISP parole model.
Receives: Behavioral: WISP supervision
Parole-as-usualActive comparatorParolees supervised under Washington State's parole-as-usual
Receives: Behavioral: Parole-as-usual

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Revocation rate

    Percentage of subjects in each condition who are revoked from parole and returned to prison

    Measured: 12 months

Secondary outcomes (5)
  1. % positive drug tests

    Percentage of random and scheduled drug tests that test positive for illicit drugs

    Measured: 12 months

  2. Days incarcerated

    Total number of days incarcerated in jail or prison

    Measured: 12 months

  3. % Missed appointments

    Percentage of parole appointments that are missed.

    Measured: 12 months

  4. New arrests

    Number of new arrests.

    Measured: 12 months

  5. Assessed risk

    Parolee risk assessment (high, medium, low)

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Apr 2011 (estimated)
  2. Study startJan 2011
  3. Primary completionJan 2012
  4. Study completionJun 2012

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
70 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01343472
Sponsor's protocol ID
SPP0311F08
Status last verified
Apr 2018
First submitted
26 Apr 2011
Last updated
10 Apr 2018
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing WISP supervision and Parole-as-usual in people with Behavior and Drug Users, run by Pepperdine University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Apr 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Revocation rate (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Apr 2018.

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