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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-06-30

Study Completion Date

2009-08-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Healthy

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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Hospital Patients/Hospital Employees

No interventions assigned to this group

Hospital employees

A group of 10 hospital employees used as baseline

No interventions assigned to this group

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes