- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01727882
Automated Telephone Follow-up in the Swedish Prison and Probation Services
November 12, 2012 updated by: Claes Andersson, Region Skane
Automated Telephone Follow-up in the Swedish Prison and Probation Services. A Randomized Controlled Trail.
The purpose of this study is to investigate whether automated telephony may be used for daily assessments of paroled offenders, and whether a brief intervention based on these daily assessments may result in a more positive development compared to daily assessments only.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
To study whether automated telephony could be used in paroled offenders to perform daily assessment of variables associated with recidivism in crime and to study the effects of a brief intervention based on these assessments during 30 days following probation.
Study Type
Interventional
Enrollment (Actual)
108
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
-
-
-
Norrköping, Sweden
- The Swedish Prison and Probation Services, Region South and Region East
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Convicted criminals subject to parole
- Access to a mobile telephone
- Assigned parole officer at parole
Exclusion Criteria:
- No knowledge of spoken Swedish
- Additional intervention such as intensive supervision with electronic monitoring, or in-patient care at a health and rehabilitation clinic
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Daily Assessments & Brief Feedback
Daily assessments during 30 days after parole and a feedback intervention based on these daily assessments.
|
A brief feedback was given on the results of the daily assessments, including a recommendation to the paroled offender and a email report was sent to the probation officer.
Daily assessment of stress, mental symptoms, alcohol and substance use during 30 consecutive days after parole.
|
|
Active Comparator: Daily assessments
Daily assessments during 30 days after parole.
|
Daily assessment of stress, mental symptoms, alcohol and substance use during 30 consecutive days after parole.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mental symptoms, SCL-8D
Time Frame: During 30 days after probation
|
Mental Symptoms, assessed with SCL-8D (Fink et al.
A Nordic multicentre investigation.
Part I: Method and prevalence of psychiatric morbidity.
Acta Psychiatrica Scandinavica.
1995;92(6):409-418).
|
During 30 days after probation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress
Time Frame: During 30 days after probation
|
Stress assessed with the Arnetz and hasson stress questionnaire(Andersson C et al.
Measurement properties of the Arnetz and Hasson stress questionnaire in Swedish university freshmen.
Scandinavian Journal of Public Health.
2009;37(3):273-279)
|
During 30 days after probation
|
|
Stress
Time Frame: During 30 days after probation
|
Daily Assessment of Daily Experience (Stone AA, Neale JM.
Development of a methodology for assessing daily experiences.
In: Baum A, Singer J, eds.
Advances in Environmental Psychology: Environment and Health.
Vol 4. New York: Erlbaum; 1982:49-83).
|
During 30 days after probation
|
|
Desire to use alcohol and drugs
Time Frame: During 30 days after probation
|
Desire to use alcohol and drugs (Bohn MJ, Krahn DD, Staehler BA.
Development and initial validation of a measure of drinking urges in abstinent alcoholics.
Alcoholism: Clinical and Experimental Research.
1995;19(3):600-606).
|
During 30 days after probation
|
|
Current use of alcohol and drugs
Time Frame: During 30 days after probation
|
Current use was then assessed by simply asking whether the offender had drunk alcohol or used any drugs the previous day.
|
During 30 days after probation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Claes Andersson, PhD, Lund university and Malmö university
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
December 1, 2009
Primary Completion (Actual)
September 1, 2010
Study Completion (Actual)
September 1, 2010
Study Registration Dates
First Submitted
November 4, 2012
First Submitted That Met QC Criteria
November 12, 2012
First Posted (Estimate)
November 16, 2012
Study Record Updates
Last Update Posted (Estimate)
November 16, 2012
Last Update Submitted That Met QC Criteria
November 12, 2012
Last Verified
November 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 535629 (Other Identifier: The Swedish Prison and Probation Services)
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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