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

Major Depressive Disorder Clinical Trial

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT00433238
• Other study ID #: WCMSH
• Status: Not yet recruiting
• Phase: Phase 1
• First received: February 7, 2007
• Last updated: February 7, 2007
• Start date: March 2007

Study information

• Verified date: February 2007
• Source: Mount Sinai Hospital, Canada
• Contact: K.C. Chan
• Phone: 416-291-3883
• Email: kcchan[@]mtsinai.on.ca
• Is FDA regulated: No
• Health authority: Canada: Ethics Review Committee
• Study type: Interventional

Clinical Trial Summary

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.

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.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 55 Years to 85 Years

Eligibility

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 Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Screening

Related Conditions & MeSH terms

• Dementia
• Depression
• Depressive Disorder
• Depressive Disorder, Major
• Major Depressive Disorder

Intervention

Behavioral:
• Participants will be screened for depression and cognitive impairment, then receive screening results.

Locations

Country	Name	City	State
Canada	Wellness Centre	Toronto	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
Mount Sinai Hospital, Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of help seeking in intervention group
Primary	Rate of confirmed psychiatric diagnoses in intervention group
Primary	Type of intervention received