MedTrace Logo

Comparison of an Electronic Version of Selected COPD PRO Instruments With the Original Versions

NCT01875302 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2013-06-19

No results posted yet for this study

Summary

This protocol defines the requirements to demonstrate that the PRO instruments which were designed as paper-based are equivalent to the nSpire Health ePRO (electronic patient reported outcome), following the ISPOR's ePRO Good Research Practices Task Force recommendations. All validation studies of the questionnaires were conducted using the original paper versions.

Conditions

Sponsors & Collaborators

  • nSpire Health, Inc.

    lead INDUSTRY

Principal Investigators

  • Michelle Vig, MS · nSpire Health

Eligibility

Min Age
40 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2013-04-30
Completion
2013-05-31

More Related Trials

Entities

Diseases

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 NCT01875302 on ClinicalTrials.gov