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N/A N=2,698 Randomized Single-blind Treatment

Using Information Technology to Improve Asthma Adherence

Asthma · Patient Compliance

Enrolled (actual)
2,698
Serious AEs
0.0%
Results posted
Aug 2010
Primary outcome: Primary: Patient Adherence to Inhaled Corticosteroids (ICS) — 21.3; 23.3 Percent of ICS medication taken

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Feedback of patient adherence information (Behavioral); Active control group (Behavioral)
Age
Pediatric, Adult · 5+ yrs
Sex
All
Sponsor
Henry Ford Health System
Primary completion
Aug 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Patient Adherence to Inhaled Corticosteroids (ICS)
21.3; 23.3
SECONDARY
Asthma-related Emergency Room Visits
SECONDARY
Asthma-related Hospitalizations
SECONDARY
Oral Steroid Use
SECONDARY
Patient Self-efficacy to ICS Treatment
SECONDARY
Readiness to Improve ICS Adherence (Transtheoretical Model)
SECONDARY
Patient-physician Communication (Patient Reported Measure)
SECONDARY
Patient Medical Care Costs

Summary

The purpose of this study is to determine whether providing patient medication adherence information on inhaled corticosteroid use to clinicians will result in improved patient adherence and asthma control.

Eligibility Criteria

Inclusion Criteria (patient-level):

  • Age 5-56 years
  • Physician diagnosis of asthma
  • Continuous HMO enrollment with prescription drug rider
  • Electronic prescription of an inhaled corticosteroid

Exclusion Criteria (patient-level):

  • Diagnosis of chronic obstructive pulmonary disease
  • Diagnosis of congestive heart failure

Inclusion Criteria (practice-level):

  • Primary care practice (i.e., pediatrics, family practice, or internal medicine) within the health system. A practice is defined as a group of physicians who by virtue of speciality or geography care for a relatively contained population of patients and who cross-cover the care of these patients.

Exclusion Criteria (practice-level):

  • None
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00459368). 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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