Health Care Management for the Elderly in Community Through Screening
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
Depression in late life has been associated with losses in functioning and quality of life, mortality, and increased health care costs. Although late life depression can be successfully treated with antidepressant medication or psychotherapy, few older adults receive adequate trials of such treatment in community in Korea. Barriers, such as loss of loved ones, medical illnesses, and social stigma associated with depression, lack of social and financial support, to effective treatment of depression can be especially problematic for older adult. Screening has been valuable in overcoming barriers to diagnosis. Over 60 year old community dwelling people will be screened for symptoms of four geriatric conditions (depression, dementia, urinary incontinence, and sleep disorder). Those who will be screened positive for each condition will be refer to clinic for diagnosis. Among them only those cases confirmed as depression by psychiatrists will be enrolled in this study. Enrolled patients will be randomly assigned to either case management or usual care conditions.
The objective of the study is to test whether a system of screening, assessment, and follow-up provided by case manager improves in recognizing the target geriatric conditions (depression, dementia, urinary incontinence, and sleep disorder) and healthcare outcomes.
| Condition | Intervention |
|---|---|
|
Major Depressive Disorders Senile; Depression |
Other: case management |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Screening |
- Geriatric Depression Score [ Time Frame: 6 months after baseline ] [ Designated as safety issue: No ]
- quality of life [ Time Frame: 6 months after baseline ] [ Designated as safety issue: No ]
- treatment compliance [ Time Frame: 6 months after baseline ] [ Designated as safety issue: No ]
- suicide ideation [ Time Frame: 6 months after baseline ] [ Designated as safety issue: No ]
| Enrollment: | 57 |
| Study Start Date: | May 2011 |
| Study Completion Date: | April 2012 |
| Primary Completion Date: | April 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: usual care
providing usual care
|
Other: case management
confirmation of hospital visit date, checking the adverse effect and treatment compliance
|
Eligibility| Ages Eligible for Study: | 60 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- over 60 year old
- having medicare insurance
Exclusion Criteria:
- dementia and other psychiatric disorders
Contacts and Locations| Korea, Republic of | |
| City of Choongju public health center | |
| Choongju, Choongchungbuk-Do, Korea, Republic of | |
| Principal Investigator: | Hyeon Woo Yim, MD. Ph.D. | The Catholic University of Korea |
More Information
No publications provided
| Responsible Party: | Hyeon Woo Yim, Professor, National Clinical Research Coordination Center, Seoul, Korea |
| ClinicalTrials.gov Identifier: | NCT01347138 History of Changes |
| Other Study ID Numbers: | A102065 |
| Study First Received: | April 27, 2011 |
| Last Updated: | March 14, 2013 |
| Health Authority: | Korea: Ministry for Health, Welfare and Family Affairs |
Keywords provided by National Clinical Research Coordination Center, Seoul, Korea:
|
Screening depression case management |
Additional relevant MeSH terms:
|
Depression Depressive Disorder Depressive Disorder, Major |
Behavioral Symptoms Mood Disorders Mental Disorders |
ClinicalTrials.gov processed this record on June 18, 2013