- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00559208
Children's Aid Societies: Differential Response and Wraparound Prevention Trial
June 22, 2011 updated by: Hamilton Children's Aid Society
The Comparative Effects and Expense of Augmenting Usual Children's Aid Society (CAS) Care With a Regional Differential Response and Wraparound Prevention Service for Children
The purpose of this study is to assess the cost-effectiveness of this Differential Wraparound model, in 5 Children's Aid Societies within Hamilton-Niagara Region, in preventing maltreatment cases from either becoming ongoing protection cases, or the children ending up in out-of-home of out-of community placements, as well as reducing the amount of time in Children's Aid Society care as compared to usual Children's Aid Society risk assessment and protection service alone.
Study Overview
Status
Completed
Conditions
Detailed Description
The number of children in child welfare care has increased from 10,000 in the early 1990s to over 18,000.
Ontario spends over $1.1 billion a year on direct child welfare services, more than twice as much as spent in the late 1990s, with the majority of these resources spent on investigation instead of treatment.
In response to this situation, Differential Response models, sometimes called alternative, multiple or integrated system responses, have been implemented in the US, Australia and Canada and are all at the beginning stages of systematic evaluation.
These models will help prevent maltreatment cases from becoming ongoing protection cases, or the children ending up in out of home or community placements, and reduce the amount of time in Children's Aid Society care.
This research will show the benefits and costs of a Differential Response approach to Children's Aid Society care, specifically in the Hamilton-Niagara Region
Study Type
Observational
Enrollment (Actual)
135
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
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Ontario
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Hamilton, Ontario, Canada, L8N 4B9
- Children's Aid Society
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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
1 year to 80 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Clients of CAS going on to protective custody cases
Description
Inclusion Criteria:
- Parent of children and youth, living in Hamilton and surrounding areas.
- Newly referred substantiated cases going on to protective services.
- English & non-English speaking.
Exclusion Criteria:
- Safety threat
- Non-substantiated cases not going to protective services.
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: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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Children's Aid Societies
Comparing differential response (Wraparound) with usual care
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
To measure the characteristics of families and their children and comparisons between usual care versus differential response
Time Frame: Follow-up at 1 year and 2 years
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Follow-up at 1 year and 2 years
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Follow up measures at 1 year and 2 year follow ups including measuring whether differential response is happening
Time Frame: 6 months after facilitator is assigned
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6 months after facilitator is assigned
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Dominic Verticchio, Children's Aid Society
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
October 1, 2006
Study Completion (Actual)
December 1, 2010
Study Registration Dates
First Submitted
November 15, 2007
First Submitted That Met QC Criteria
November 15, 2007
First Posted (Estimate)
November 16, 2007
Study Record Updates
Last Update Posted (Estimate)
June 23, 2011
Last Update Submitted That Met QC Criteria
June 22, 2011
Last Verified
November 1, 2009
More Information
Terms related to this study
Other Study ID Numbers
- 06-103
- NCT00397085 (Other Grant/Funding Number: Ministry of Children & Youth 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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