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Screening for Mental Health Concerns for at-Risk Community Living Chinese Seniors

Primary Purpose

Major Depressive Disorder, Dementia

Status
Unknown status
Phase
Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Participants will be screened for depression and cognitive impairment, then receive screening results.
Sponsored by
Mount Sinai Hospital, Canada
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional screening trial for Major Depressive Disorder focused on measuring elderly, Chinese, community living, measurement, depression, dementia, Geriatric Depression Scale, MiniCog

Eligibility Criteria

55 Years - 85 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • capable of providing informed consent
  • informed consent

Exclusion Criteria:

  • Individuals who are unable to fully understand the nature of the study, its possible risks and benefits and the consequences of providing or withholding consent, and who are, therefore, not capable of providing informed consent will be excluded from the study.

Sites / Locations

  • Wellness Centre

Outcomes

Primary Outcome Measures

Rate of help seeking in intervention group
Rate of confirmed psychiatric diagnoses in intervention group
Type of intervention received

Secondary Outcome Measures

Full Information

First Posted
February 7, 2007
Last Updated
February 7, 2007
Sponsor
Mount Sinai Hospital, Canada
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1. Study Identification

Unique Protocol Identification Number
NCT00433238
Brief Title
Screening for Mental Health Concerns for at-Risk Community Living Chinese Seniors
Official Title
Screening for Mental Health Concerns for at-Risk Community Living Chinese Seniors - a Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2007
Overall Recruitment Status
Unknown status
Study Start Date
March 2007 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Mount Sinai Hospital, Canada

4. Oversight

5. Study Description

Brief Summary
The study is designed to answer the following research questions: Evaluate the acceptability of mental health screening and of the instruments used in a sample of community living Chinese seniors; Determine rates of mental health service utilization in individuals identified at screening as having psychological disturbance; Determine if identifying mental illness and informing participants of screening results and with treatment alternatives alters help-seeking pathways. The study hypotheses are: This community sample of Chinese seniors will show a higher prevalence of psychological disturbance than their counterparts in the general population; Emotional well-being will be positively correlated with individuals' physical health and social support network.
Detailed Description
A convenience sample will be drawn from 6 Congregate Dining (CD) groups in the Chinese community. There are six groups of CD programs run by Yee Hong Centre for Geriatric Care run at different locations in the Greater Toronto Area. The screening will be offered on site at regular CD meetings to participants who have given informed, written consent. All participants will attend a private post-screening interview. Those who score above the threshold for depression and/or cognitive impairment, and who have not previously been diagnosed or treated for these conditions, will be randomly assigned to one of two groups: an intervention group and a usual care group. Participants in the intervention group will receive their screening results at the post-screening interviews and will also be provided with suggestions for possible follow-up. They will be given the option of receiving further psychiatric assessment at the Wellness Centre, or seeking care with their family physician and assisted to obtain further care, if desired. Participants in the intervention group will attend an appointment 3 months after receiving screening results and follow-up options during which the rate of help seeking, rate of confirmed psychiatric diagnoses and types of intervention received will be determined. Participants in the usual care group will not be given screening results at the post-screening interview but will instead attend an appointment 3 months post screening to receive their results and information about follow-up options. The results of this research will: demonstrate whether community living Chinese elders are at greater risk of psychiatric disorders and demonstrate the need for screening in older Chinese adults living in the community; aid in the development of systematic and targeted community-based screening and outreach to at-risk members of the target population; and help determine if identification of mental health issues and education about treatment resources has any effect on help-seeking for those conditions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder, Dementia
Keywords
elderly, Chinese, community living, measurement, depression, dementia, Geriatric Depression Scale, MiniCog

7. Study Design

Primary Purpose
Screening
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
100 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Participants will be screened for depression and cognitive impairment, then receive screening results.
Primary Outcome Measure Information:
Title
Rate of help seeking in intervention group
Title
Rate of confirmed psychiatric diagnoses in intervention group
Title
Type of intervention received

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: capable of providing informed consent informed consent Exclusion Criteria: Individuals who are unable to fully understand the nature of the study, its possible risks and benefits and the consequences of providing or withholding consent, and who are, therefore, not capable of providing informed consent will be excluded from the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
K.C. Chan
Phone
416-291-3883
Ext
225
Email
kcchan@mtsinai.on.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Joel Sadavoy, M.D.
Phone
416-586-4800
Ext
5262
Email
jsadavoy@mtsinai.on.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joel Sadavoy, M.D.
Organizational Affiliation
Mt. Sinai Hospital, Toronto, Canada
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wellness Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M1V5L6
Country
Canada
Facility Contact:
First Name & Middle Initial & Last Name & Degree
K.C. Chan

12. IPD Sharing Statement

Learn more about this trial

Screening for Mental Health Concerns for at-Risk Community Living Chinese Seniors

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