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

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00921466

Acronym

e-SSRS-IVR

Enrollment

Registered

2009-06-16

Start date

2009-06-30

Completion date

2009-08-31

Last updated

2009-06-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

Evaluate the clinical content of the e-SSRS-IVR

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.

Interventions

None listed

Study design

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Yes

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

Countries

United States

Outcome results