An Educational Intervention to Improve Disease Management Knowledge of Hospitalized Patients With COPD



Status:Recruiting
Conditions:Chronic Obstructive Pulmonary Disease, Pulmonary
Therapuetic Areas:Pulmonary / Respiratory Diseases
Healthy:No
Age Range:18 - Any
Updated:10/28/2017
Start Date:August 30, 2016
End Date:January 31, 2019
Contact:Tyler Weiss
Email:Tyler_Weiss@rush.edu
Phone:312-563-2050

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The objective of this study is to determine if inpatient COPD education would result in
improved patient knowledge of COPD.

A prospective cohort study utilizing a pre-test/post-test design will be used to test a COPD
education intervention on a convenience sample of 30 patients with a diagnosis of COPD. Study
participants will complete the Chronic Obstructive Pulmonary Disease questionnaire (COPD-Q)
to assess their COPD knowledge. Next, a respiratory therapist will provide the first scripted
COPD education session. The patient will complete the COPD-Q 24 hours and 30 days
post-discharge. Demographic data, smoking status, pack-years, COPD spirometry grade, COPD
symptom and exacerbation grade, previous hospital admissions, support system for managing
COPD, attendance at previous formal education for COPD, current and home medications,
pulmonary function test (PFT) results, vaccinations, and level of education data will be
collected. Data related to patient recruitment will also be collected. Means and standard
deviation will be reported for interval data. Total frequency and percentages will be
reported for nominal data, and median and 25th and 75th percentile will be reported for COPD
severity. Repeated measures ANOVA (p< 0.05) will be used to evaluate if an inpatient COPD
self-management intervention can increase the patient's knowledge of COPD after 24 hours and
again at 30 days after the initial education session.

This study is expected to show that an inpatient education of COPD can increase the patient's
COPD knowledge prior to discharge and that it will be retained for at least one month
post-discharge.

Inclusion Criteria:

- History of COPD

- Spirometry confirmation of COPD either from chart or bedside spirometry i. FEV1(forced
expiatory volume in 1 second)/FVC (forced vital capacity) <70% ii. FEV1 < 80%
predicted

- Willingness to participate

- English-speaking

- Working phone

Exclusion Criteria:

- Cognitively impaired (including sedation)

- Intubated

- Non-English-speaking

- Receiving palliative or hospice service

- Enrolled in any other educational research s
We found this trial at
1
site
1653 W. Congress Parkway
Chicago, Illinois 60612
(312) 942-5000
Principal Investigator: Tyler Weiss, MS
Phone: 312-563-2050
Rush University Medical Center Rush University Medical Center encompasses a 664-bed hospital serving adults and...
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from
Chicago, IL
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