Depression Clinical Trial
Official title:
Examining the Feasibility and Effectiveness of Case Manager Delivered Problem Solving Therapy on Late Life Depression; an Open-label Prospective Pilot Study.
Verified date | March 2018 |
Source | Lawson Health Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study seeks to determine the feasibility and efficacy of a Problem Solving Therapy intervention for the treatment of late life depression (LLD). Participants diagnosed with LLD will participate in six sessions of Problem Solving Therapy, a form of talk-therapy, over a period of eight weeks. A Case Manager (CM) will lead the PST. The primary outcome measure is depression severity and will be measured throughout the study at weeks 0, 4, and 8. the secondary outcome measure is quality of life and will be measured at week 0 (pre-intervention) and week 12.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | October 2019 |
Est. primary completion date | October 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 60 Years to 85 Years |
Eligibility |
Inclusion Criteria: - Are of either gender and greater than 60 years of age. - Reside in a community setting (either independent living environment or retirement home). - Meet diagnostic criteria for major depressive disorder (MDD) according to the Diagnostic and Statistical Manual of Mental Disorders-V (DSM-V) criteria. - Have a Hamilton Depression Rating Scale (HAMD) 17-item total score of >= 8 and < 24 at baseline. - Have a Mini Mental Status Exam score of >= 20. - Have adequate hearing and vision to be able to participate in Problem Solving Therapy. Exclusion Criteria: - Have suicidal ideation requiring inpatient admission to hospital for stabilization. - Have an unstable medical condition requiring hospital admission. - Have a life expectancy of less than 6 months or are currently receiving palliative care. - Have psychotic symptoms. - Have a lifetime history of bipolar disorder or schizophrenia. - Are currently alcohol dependent or have another substance dependence. - Are diagnosed with moderate to severe dementia. - Are planning admission to a long-term care facility within next 6 months. |
Country | Name | City | State |
---|---|---|---|
Canada | London Health Sciences Centre | London | Ontario |
Lead Sponsor | Collaborator |
---|---|
Lawson Health Research Institute | Queen's University, University of Western Ontario, Canada |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in depression symptoms | Depression in study participants will be self rated on the Patient Health Questionnaire (PHQ-9) | Baseline, week 4, and week 8 | |
Secondary | Change in Quality of Life | Participants will complete a Short Form-12 to assess the change in their quality of life. | Baseline and week 12 | |
Secondary | Change in Depression Symptoms- Clinician Rated | Hamilton scale for Depression-17 item (HAM-D 17), as rated by a clinician trained to complete this scale | Baseline, Week 4 and Week 8 | |
Secondary | Change in Depression Symptoms- Overall improvement | Clinical Global Impression- CGI, as rated by a clinician trained to complete this scale | Baseline, Week 4 and Week 8 |
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