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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT00921466
Other study ID # 113235
Secondary ID
Status Enrolling by invitation
Phase N/A
First received June 15, 2009
Last updated June 15, 2009
Start date June 2009
Est. completion date August 2009

Study information

Verified date June 2009
Source Rogers Center for Research & Training, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Rogers Center for Research and Training, Inc Milwaukee Wisconsin

Sponsors (2)

Lead Sponsor Collaborator
Rogers Center for Research & Training, Inc. GlaxoSmithKline

Country where clinical trial is conducted

United States, 

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