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

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

The study is designed to answer the following research questions:

1. Evaluate the acceptability of mental health screening and of the instruments used in a sample of community living Chinese seniors;
2. Determine rates of mental health service utilization in individuals identified at screening as having psychological disturbance;
3. Determine if identifying mental illness and informing participants of screening results and with treatment alternatives alters help-seeking pathways.

The study hypotheses are:

1. This community sample of Chinese seniors will show a higher prevalence of psychological disturbance than their counterparts in the general population;
2. Emotional well-being will be positively correlated with individuals' physical health and social support network.

Study Overview

• Status: Unknown
• Conditions: Dementia; Major Depressive Disorder
• Intervention / Treatment: Behavioral: Participants will be screened for depression and cognitive impairment, then receive screening results.

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.

• Study Type: Interventional
• Enrollment: 100
• Phase: Phase 1

Contacts and Locations

Study Locations

• Canada
  • Ontario
    • Toronto, Ontario, Canada, M1V5L6
      • Wellness Centre

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 55 years to 85 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

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.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Screening
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

What is the study measuring?

Primary Outcome Measures

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

Collaborators and Investigators

• Sponsor: Mount Sinai Hospital, Canada
• Investigators: Principal Investigator: Joel Sadavoy, M.D., Mt. Sinai Hospital, Toronto, Canada

Study record dates

Study Major Dates

• Study Start: March 1, 2007

Study Registration Dates

• First Submitted: February 7, 2007
• First Submitted That Met QC Criteria: February 7, 2007
• First Posted (Estimate): February 9, 2007

Study Record Updates

• Last Update Posted (Estimate): February 9, 2007
• Last Update Submitted That Met QC Criteria: February 7, 2007
• Last Verified: February 1, 2007

More Information

Terms related to this study

• Keywords: dementia; depression; Chinese; elderly; measurement; Geriatric Depression Scale; community living; MiniCog
• Additional Relevant MeSH Terms: Mental Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Mood Disorders; Neurocognitive Disorders; Depressive Disorder; Dementia; Depressive Disorder, Major
• Other Study ID Numbers: WCMSH