Pilot Study to Assess Feasibility, Reliability and Validity of the e-SSRS-IVR

• Conditions: Healthy

• Registration Number: NCT00921466
• Lead Sponsor: Rogers Center for Research & Training, Inc.

Brief 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.

Detailed Description

Not available

Study Timeline

• Status Verified: 2009-06
• Study Start: 2009-06
• Study First Submitted: 2009-06-15
• Study First Submitted QC: 2009-06-15
• Last Update Submitted: 2009-06-15
• Study First Posted: 2009-06-16
• Last Update Posted: 2009-06-16
• Primary Completion: 2009-07
• Study Completion: 2009-08

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 20

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

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

Rogers Center for Research and Training, Inc; 🇺🇸 Milwaukee, Wisconsin, United States