Office-Based Asthma Screening Intervention
This study has been completed.
Sponsor:
University of Rochester
Collaborators:
Halcyon Hill Foundation
Robert Wood Johnson Foundation
Information provided by:
University of Rochester
ClinicalTrials.gov Identifier:
NCT00156468
First received: September 8, 2005
Last updated: May 11, 2011
Last verified: May 2011
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Purpose
In prior work, we found that even children who have been seen by their physicians within the prior six months were frequently misclassified as having mild rather than persistent asthma. This study evaluations whether systematic office-based screening assists primary care physicians in identifying children with significant asthma and improves preventive care for asthma. We hypothesize that standardized screening in the office setting will improve the physician's ability to (a) identify children with significant asthma and (b) prescribe appropriate preventive medications.
| Condition | Intervention |
|---|---|
|
Asthma |
Behavioral: Provider Prompt |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single Blind Primary Purpose: Prevention |
| Official Title: | Office-Based Asthma Screening Intervention |
Resource links provided by NLM:
Further study details as provided by University of Rochester:
Primary Outcome Measures:
- "Preventive Medication Actions (PMA)" taken by the provider at the time of the child's visit. A "PMA" is defined as a new medication prescription or change in medication dose.
Secondary Outcome Measures:
- Alternate actions taken by the provider such as: discussion of environmental controls, medication refills, etc.
| Estimated Enrollment: | 365 |
| Study Start Date: | October 2003 |
| Estimated Study Completion Date: | September 2005 |
Eligibility| Ages Eligible for Study: | 2 Years to 12 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Children ages 2-12
- Children arriving for an office visit in two Rochester, NY pediatric clinics
- Children with a prior diagnosis of asthma AND an exacerbation of symptoms within the previous 2 years
Exclusion Criteria:
- Children arriving at the office visit with an adult that is not their parent or guardian
- Children arriving at the office visit with a parent or guardian that does not speak English
- Children with other medical conditions making the assessment of asthma severity difficult (cystic fibrosis, heart conditions, etc.)
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00156468
Locations
| United States, New York | |
| University of Rochester | |
| Rochester, New York, United States, 14642 | |
Sponsors and Collaborators
University of Rochester
Halcyon Hill Foundation
Robert Wood Johnson Foundation
Investigators
| Principal Investigator: | Jill S Halterman, MD, MPH | University of Rochester |
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00156468 History of Changes |
| Other Study ID Numbers: | 10035 |
| Study First Received: | September 8, 2005 |
| Last Updated: | May 11, 2011 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Asthma Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases |
Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |
ClinicalTrials.gov processed this record on May 22, 2013