Screening Clinical Trial
— CaPRAOfficial title:
Computer-assisted Psychosocial Risk Assessment (CaPRA) for Refugee Health and Settlement - Evaluation Phase
Verified date | August 2011 |
Source | University of Toronto |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Health Canada |
Study type | Interventional |
The purpose of this study was to examine preliminary effect of Computer-assisted Psychosocial Risk Assessment tool (CaPRA) among Afghan refugees visiting medical professionals (family physicians or nurse practitioners) at a Community Health Center. The investigators examined the tool's acceptability among patients and its impact on patient satisfaction and patient intention to visit a psychosocial counselor as a proxy of potential to integrate medical and social care.
Status | Completed |
Enrollment | 50 |
Est. completion date | October 2010 |
Est. primary completion date | October 2010 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Afghan refugee patients - Over 18 years of age - Speak and read Dari /Farsi or English language - Eligible for federal or provincial health care program - Visiting a participating medical practitioner Exclusion Criteria: - Patient visiting a provider who has not consented for the study - Patient accompanied by a family member for interpretation - New patients - Patients unable to receive study details due to logistical issue (e.g, no private room) |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Toronto |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Patient intention to visit a psychosocial counselor | Patients completed a paper-pencil Exit Survey in the intervention (CaPRA) and control (usual care) groups | July to October post-visit | No |
Secondary | Patient satisfaction | Patients completed a paper-pencil Exit Survey in the intervention (CaPRA) and control (usual care) groups | July to October post-visit | No |
Secondary | Patient acceptability | Patients completed a paper-pencil Exit Survey in the intervention group (CaPRA) | July to October post-visit | No |
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