- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00580476
Assessing Depression in a Geriatric Cancer Population
Study Overview
Status
Conditions
Detailed Description
We have a few questionnaires that have been used to measure depression, but we do not know how these measures work with people with cancer. This study will help us answer this question. To complete this study, we need people who may or may not be feeling down or depressed.
If you choose to take part, you will be asked to do the following:
Fill out questionnaires that ask about:
- Your age, eduction, race, and income
- Your mood
In all, these questionnaires will take about 10 minutes to complete.
- Answer questions about your mood. This will also take about 10 minutes to complete.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
New York
-
New York, New York, United States, 10065
- Memorial Sloan Kettering Cancer Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age 70 and older
- Diagnosis of early or late stage prostate cancer, or diagnosis of early or late stage breast cancer
- Actively engaged in one of the following cancer treatments: chemotherapy, radiation therapy, hormone therapy
- Able to provide informed consent
- Ability to converse, write and read English
Exclusion Criteria:
1.Major psychopathology or cognitive impairment likely in the judgment of the research staff to interfere with the participation or completion of the protocol.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
1
150 patients will be women with breast cancer (75 early stage and 75 late stage)
|
|
2
150 will be men with prostate cancer (75 early stage and 75 late stage)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Test the sensitivity and specificity of the Geriatric Depression Scale-Short Form and two other widely used assessments of depression to detect major and minor depression in a geriatric breast and prostate cancer population.
Time Frame: 2 years
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
To develop a cut-off score for the GDS that is specific to a cancer population.
Time Frame: 2 years
|
2 years
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Christian Nelson, Ph.D., Memorial Sloan Kettering Cancer Center
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 06-100
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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