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

NCT00921466 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2009-06-16

No results posted yet for this study

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.

Conditions

  • Healthy

Sponsors & Collaborators

  • GlaxoSmithKline

    collaborator INDUSTRY

  • Rogers Center for Research & Training, Inc.

    lead OTHER

Principal Investigators

  • John H Greist, MD · Rogers center for Research and Training, Inc

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2009-07-31
Completion
2009-08-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00921466 on ClinicalTrials.gov