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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01775683
Other study ID # 20120651-01H
Secondary ID
Status Not yet recruiting
Phase N/A
First received September 25, 2012
Last updated January 22, 2013
Start date January 2013
Est. completion date September 2013

Study information

Verified date January 2013
Source Ottawa Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Observational

Clinical Trial Summary

Homeless men and women suffer more illness and sooner death compared to housed people. Among the homeless, there is a group that suffers more illness than others. This group is usually homeless for several months, makes up a smaller proportion of homeless people and uses more resources from emergency shelters than other homeless people. Some have asked if a difference in thinking skills explains how people who are homeless for a long time need more help in getting and keeping housing compared to other homeless persons.

In this study, thinking skills that help a person plan and make decisions will be screened among those who have been homeless for a long time and those who were homeless for a short time. If there is a difference, then screening may change how future homeless people get the help they need.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date September 2013
Est. primary completion date September 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Men and women, greater than or equal to 18 years old, English speaking

- Group A: currently homeless and/or housed in an emergency shelter or housing facility for chronically homeless individuals = 6 months

- Group B: not homeless =4 times in the last 3 years and currently living in stable housing = 6 months and in the last 3 years, has been homeless = 1 month

Exclusion Criteria:

At the time of testing, individuals with the following characteristics will be excluded:

1. Altered mental status (determined by Nurse Coordinator through participant response to questions regarding orientation to person, place and season - score of at least 2/3 is considered intact mental status).

2. Present intoxication (determined by Nurse Coordinator through participant evaluation of odour, either alcohol or non-beverage alcohol).

3. Currently violent or aggressive towards testers (determined by Nurse Coordinator)

Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Canada The Ottawa Hospital Rehabilitation Centre Ottawa Ontario

Sponsors (1)

Lead Sponsor Collaborator
Ottawa Hospital Research Institute

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Quick EXIT score Within 2 weeks of recruitment No
Secondary The Colour Trails test score Within 2 weeks of recruitment No
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