Healthy Clinical Trial
— e-SSRS-IVROfficial title:
Pilot Study to Assess Feasibility, Reliability and Validity of the e-SSRS-IVR
The proposed study is designed to evaluate the clinical contents of the e-SSRS-IVR with respect to 1.the intent of the instrument (assess face and content validity), 2. system validation with respect to programming integrity, 3. implementation feasibility in clinical ill and healthy patient populations, and 4. criterion/predictive validity to discriminate patient population with known clinical status differences.
Status | Enrolling by invitation |
Enrollment | 20 |
Est. completion date | August 2009 |
Est. primary completion date | July 2009 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - English speaking adults, able/willing to read and provide written consent Exclusion Criteria: - Dementia, delirium, psychosis or deafness. - Control subjects will be excluded for any MINI lifetime MDD or dysthymia diagnosis of a DSM-IV disorder except for specific phobia or dependence on nicotine and caffeine. - Inpatients not admitted with suicidal ideations |
Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Rogers Center for Research and Training, Inc | Milwaukee | Wisconsin |
Lead Sponsor | Collaborator |
---|---|
Rogers Center for Research & Training, Inc. | GlaxoSmithKline |
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