The Provider and Organization in Asthma Guidelines
2 other identifiers
interventional
36
1 country
1
Brief Summary
The purpose of this study is to examine the interaction between the personal attributes of clinicians and the organizations in which they work and the effect of interventions on their ability to implement an asthma disease management program. +
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable asthma
Started Sep 2002
Longer than P75 for not_applicable asthma
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2002
CompletedFirst Submitted
Initial submission to the registry
June 27, 2006
CompletedFirst Posted
Study publicly available on registry
June 28, 2006
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2012
CompletedNovember 9, 2012
November 1, 2012
10 years
June 27, 2006
November 8, 2012
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of Easy Breathing Surveys Distributed
4 years
Secondary Outcomes (1)
Organizational Culture
baseline; 12 months and 36 months after intervention phase
Study Arms (3)
1
NO INTERVENTION2
ACTIVE COMPARATOR3
ACTIVE COMPARATORInterventions
The arm emphasized individual provider behavior (interactive CME, feedback at the provider, clinic and program levels, expert modeling, academic detailing and opinion leaders)
Leadership, team building, benchmarking at the clinic and program level
Eligibility Criteria
You may qualify if:
- Must have used Easy Breathing Disease Management Program for more than one year.
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- UConn Healthlead
- National Heart, Lung, and Blood Institute (NHLBI)collaborator
Study Sites (1)
University of Connecticut Health Center
Farmington, Connecticut, 06030, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Michelle M Cloutier, MD
UConn Health
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Pediatrics
Study Record Dates
First Submitted
June 27, 2006
First Posted
June 28, 2006
Study Start
September 1, 2002
Primary Completion
September 1, 2012
Study Completion
September 1, 2012
Last Updated
November 9, 2012
Record last verified: 2012-11