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

Rogers Center for Research & Training, Inc.

Status: Unknown

Conditions: Healthy

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT00921466

113235

Details and patient eligibility

About

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.

Enrollment: 20 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

20 participants in 2 patient groups

Hospital Patients/Hospital Employees

Hospital employees

Description:

A group of 10 hospital employees used as baseline