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Portable Oxygen Concentrator to Improve Quality of Life in Chronic Obstructive Pulmonary Disease

NCT01948544 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 27

Last updated 2018-08-20

No results posted yet for this study

Summary

* Evaluate subjects in an prospective observational study
* Subjects will be administered scientifically validated questionnaires
* Determine the affect of the Portable Oxygen Concentrator (POC) on improvements in:

1. Exercise capability, dyspnea and quality of life as primary endpoints
2. Utilize:

1. Baseline Dyspnea Index (BDI)
2. Transitional Dyspnea Index (TDI)
3. Chronic Respiratory Disease Questionnaire (CRQ)
4. Six minute walk test (6MWT)
5. Epworth Sleepiness Scale (ESS)
* The secondary endpoints will be:

1. Rate of exacerbations, sleep quality
2. Health care utilization (emergency room encounters, hospital admissions)

Conditions

Sponsors & Collaborators

  • StratiHealth

    lead INDUSTRY

Principal Investigators

  • Isabel Pereira, MD · Tri-City Medical Center

Eligibility

Min Age
65 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2014-04-30
Completion
2014-04-30

Countries

  • United States

Study Locations

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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 NCT01948544 on ClinicalTrials.gov