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Clinical Trials/NCT03323190
NCT03323190
Withdrawn
N/A

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

Rush University Medical Center1 site in 1 countryAugust 30, 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
Rush University Medical Center
Locations
1
Primary Endpoint
Gained knowledge
Status
Withdrawn
Last Updated
5 years ago

Overview

Brief Summary

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

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
August 30, 2016
End Date
August 30, 2017
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Gained knowledge

Time Frame: 1 year

Change from baseline on the Chronic Obstructive Pulmonary Disease Questionnaire (COPD-Q).

Secondary Outcomes

  • Pulmonary rehab enrollment(1 year)

Study Sites (1)

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