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N/A N=120 Randomized Single-blind Other

Effectiveness of Interventions to Teach Respiratory Inhaler Technique (E-TRaIN)

Asthma · Chronic Obstructive Pulmonary Disease (COPD)

Enrolled (actual)
120
Serious AEs
0.0%
Results posted
Oct 2019
Primary outcome: Primary: Percentage of Participants With MDI Misuse From Baseline to 30 Days Post-Discharge — 92; 84; 11; 60 percentage

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Teach-To-Goal (Behavioral); Brief Intervention (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Chicago
Primary completion
Dec 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants With MDI Misuse From Baseline to 30 Days Post-Discharge
92; 84; 11; 60
SECONDARY
Role of Health Literacy - Number of Less-Than-Adequate Health Literacy Participants With 30 Days Post Discharge Acute-Care Events
2; 7
SECONDARY
Number of Participants With Self-Efficacy
49; 38
SECONDARY
Symptom Control
-1.69; -1.43
SECONDARY
Number of Participants With Acute Care Events 30 Days Post Discharge
9; 19

Summary

The purpose of this study is to evaluate the relative effectiveness of two different ways to teach subjects while hospitalized how to use respiratory inhalers and to follow-up after discharge home from the hospital to determine durability of the education. Teach-to-Goal (TTG) education employs instruction followed by patient "teach-back," then repeated cycles of learning and assessment until a skill is mastered. By contrast, Brief Intervention (BI) education only consists of providing the patient with verbal and written instruction. The investigators hypothesize that hospital-based TTG compared to BI increases a patient's ability to retain instructions on respiratory inhaler technique. The investigators will test this hypothesis separately for the MDI and Diskus® devices after discharge.

Eligibility Criteria

Inclusion Criteria

  • 18 years and older
  • Admitting diagnosis of asthma or COPD
  • Physician- diagnosed asthma, asthma/COPD, or COPD. We will enroll patients even if the primary reason for admission is not asthma or COPD (e.g., patients admitted for heart failure, but with a physician diagnosis of COPD are eligible)
  • Patient will be discharged home on a Metered Dose Inhaler (MDI; e.g., albuterol)

Exclusion Criteria

  • Currently in an intensive care unit
  • Physician declines to provide consent
  • Patient unable to provide consent (e.g., history of cognitive impairment, unable to understand English) or declines to provide consent
  • Previous participant in this study
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01426581). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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