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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00559208
Other study ID # 06-103
Secondary ID
Status Completed
Phase N/A
First received November 15, 2007
Last updated June 22, 2011
Start date October 2006
Est. completion date December 2010

Study information

Verified date November 2009
Source Hamilton Children's Aid Society
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Observational

Clinical Trial Summary

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.


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


Other known NCT identifiers
  • NCT00397085

Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date December 2010
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 1 Year to 80 Years
Eligibility 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 Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Canada Children's Aid Society Hamilton Ontario

Sponsors (2)

Lead Sponsor Collaborator
Hamilton Children's Aid Society McMaster University

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary To measure the characteristics of families and their children and comparisons between usual care versus differential response Follow-up at 1 year and 2 years Yes
Secondary Follow up measures at 1 year and 2 year follow ups including measuring whether differential response is happening 6 months after facilitator is assigned Yes
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