Depression Clinical Trial
Official title:
Effect of a Self-care Intervention on Depression in People With Age-related Macular Degeneration or Diabetic Retinopathy
Verified date | November 2016 |
Source | Maisonneuve-Rosemont Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Health Canada |
Study type | Interventional |
The purpose of this trial is to determine the short-term effect of a self-care intervention on depression in patients with age-related macular degeneration or diabetic retinopathy.
Status | Completed |
Enrollment | 80 |
Est. completion date | February 2016 |
Est. primary completion date | February 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 50 Years and older |
Eligibility |
Inclusion Criteria: - clinical diagnosis of wet or dry AMD or diabetic retinopathy - age 50 years and older - at least mild depressive symptoms (a score of 5 or more on the PHQ-9) - no legal blindness (visual acuity better than 20/200 in better eye). Exclusion Criteria: - the current use of cognitive behavioural therapy - suicidal intent - ocular surgery during the study period (intravitreal anti-VEGF injections will be allowed, e.g. Lucentis) - cognitive impairment - inability to speak and understand French or English - profound hearing impairment. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Canada | Maisonneuve-Rosemont Hospital | Montreal | Quebec |
Lead Sponsor | Collaborator |
---|---|
Maisonneuve-Rosemont Hospital | Fondation Antoine Turmel, Fonds de la Recherche en Santé du Québec |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in depressive symptoms | Depressive symptoms will be measured by the PHQ-9, a validated 9 item instrument. | Baseline and 8 weeks | No |
Secondary | Change in severity of anxiety symptoms | The GAD-7 can be used to establish probable diagnoses of generalized anxiety disorder as well as grade its severity (mild, moderate and severe). | Baseline and 8 weeks | No |
Secondary | Change in self-efficacy | Self-efficacy will be measured with a 4-item scale, adapted from a validated diabetes self-care self-efficacy scale. Scores range from 0-12. | Baseline and 8 weeks | No |
Secondary | Change in life space | The Life Space Assessment asks about the spatial extent in which the participant has traveled over the last month. Scores range from 0-100. | Baseline and 8 weeks | No |
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