NCT01427829

Brief Summary

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.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2010

Shorter than P25 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2010

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2010

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2010

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

August 22, 2011

Completed
11 days until next milestone

First Posted

Study publicly available on registry

September 2, 2011

Completed
Last Updated

September 2, 2011

Status Verified

August 1, 2011

Enrollment Period

3 months

First QC Date

August 22, 2011

Last Update Submit

September 1, 2011

Conditions

Keywords

pilotrandomized controlled trialRCTcomputerscreeningcommunity heath centerpsychosocialimmigrant

Outcome Measures

Primary Outcomes (1)

  • 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

Secondary Outcomes (2)

  • Patient satisfaction

    July to October post-visit

  • Patient acceptability

    July to October post-visit

Study Arms (2)

Intervention (CaPRA)

EXPERIMENTAL
Behavioral: Computer-assisted Psychosocial Risk Assessment (CaPRA)

Control (usual care)

NO INTERVENTION
Behavioral: Computer-assisted Psychosocial Risk Assessment (CaPRA)

Interventions

The study intervention was a touch-screen self-assessment survey which eligible patients completed on a touch-screen iPad in Dari/Farsi language while waiting to see their medical practitioner. The Computer-assisted Psychosocial Risk Assessment (CaPRA) survey had questions on psychosocial risks (e.g., alcohol, tobacco and street drug use, sexual health, personal violence, post-traumatic stress disorder, depression, and food insecurity), cardiovascular risks (e.g., physical activity, weight, diabetes, and hypertension), road and home safety, stress buffers (e.g., coping and social support) and sociodemographics. The tool generated two tailored print-outs at the point of care. The recommendation sheet for patients summarized their disclosed risks in simple Dari/Farsi language along with contacts of relevant services. The risk-report for medical practitioner summarized patients' risks with possible referrals. This was attached to the medical chart prior to the consult.

Control (usual care)Intervention (CaPRA)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Farah Ahmad, MBBS, MPH, PhD

    University of Toronto / York University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 22, 2011

First Posted

September 2, 2011

Study Start

July 1, 2010

Primary Completion

October 1, 2010

Study Completion

October 1, 2010

Last Updated

September 2, 2011

Record last verified: 2011-08