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

Status unconfirmed

Conditions studied: Healthy

In brief

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.

Key facts

Study ID

NCT00921466

Run by

Rogers Center for Research & Training, Inc.

People needed

20

Starts

2009-06-01

Expected to finish

2009-08-01

Last updated by the study team

2009-06-16

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• English speaking adults, able/willing to read and provide written consent

You may not qualify if…

• 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

Where it is running

• Rogers Center for Research and Training, Inc — Milwaukee, Wisconsin, United States

Full record on ClinicalTrials.gov

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