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Adolescent
Depression Study:
Data Sheet, Study Flow,
Data Collection Tips, FAQs |
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Overview:
This study is designed to evaluate the prevalence of depression in
adolescent (13 - 17 y.o.) patients presenting to Emergency
Department. Patients are screened for depression using the
Beck Depression Inventory. |
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Primary Endpoints:
1. Depression as assessed by Beck Depression Inventory 2.
Demographic and behavioral correlates. |
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Eligible Patients:
The patient must be between 13 and 17 years old and be in stable
medical condition. Patient MUST be accompanied by legal
guardian able to consent OR be an
emancipated minor. |
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Study Design:
Prospective observational |
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Anticipated Benefits:
If child's screening test indicates that they may be depressed, the
parents will be given more information about the test and what it
means. In addition, they will be given a list of doctors and
counselors that they can see for further evaluation. |
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Potential Risks:
A positive screening for depression may induce feelings of
anxiety, embarrassment, or stress in the patient. The test
results may also be wrong, meaning that a depressed child is missed
by the screening or vice versa. |
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Research Associate’s Role:
The RA will identify and enroll eligible patients. The RA
will need to obtain the CONSENT of the parent/guardian and ASSENT of
the patient. RA needs to ask the patient the Beck Depression
Inventory and to ask the parent/guardian the parent questionnaire. |
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Physician’s Role:
If the patient screens as "suicidal", the physician needs to further
evaluate the patient and consider an admission to CIC. |
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Location of Study Packets:
Special Care |