Evaluating the Effectiveness of the Acute Respiratory Infection Smart Form
NCT ID: NCT00235040
Last Updated: 2012-01-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
18257 participants
INTERVENTIONAL
2005-11-30
2007-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparing ASHC and CDSMP Outcomes In Arthritis
NCT00207441
A Prospective Virtual Study of Patient Reported Behaviors and Health Outcomes in Individuals With COVID-19
NCT05042232
Reimagining Interventions for Support and Education in Hypersensitivity Pneumonitis
NCT06811389
The Management of Work-Disability Associated With Co-Morbid Pain and Depression: A Feasibility Study
NCT05174429
Chronic-disease Self-management Program in Patients Living With Long-COVID in Puerto Rico
NCT06208696
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Hypothesis 1: A documentation-based clinical decision support tool (CDSS) "smart form" physician feedback system, can be designed and implemented to facilitate documentation and physician order-entry, provide individualized, evidence-based recommendations for the management of patients acute respiratory infections (ARIs), and are usable by primary care physicians.
Specific Aim 2: To determine the effectiveness of documentation-based CDSS and physician feedback on documentation and the clinical management of patients respiratory tract infections.
Hypothesis 2A: A documentation-based CDSS "smart form" will increase the documentation of important clinical data in patients with ARI when compared to usual practice.
Hypothesis 2B: A documentation-based CDSS "smart form" will increase adherence with guidelines for the management of patients with ARI when compared to usual practice.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
Intervention
Smart Form
Computer Decision Support System
2
Control
Smart Form
Computer Decision Support System
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Smart Form
Computer Decision Support System
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Agency for Healthcare Research and Quality (AHRQ)
FED
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Partners Healthcare Systems, Inc.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Blackford Middleton, MD, MPH, MSc
Role: PRINCIPAL_INVESTIGATOR
Partners Healthcare Systems Inc
References
Explore related publications, articles, or registry entries linked to this study.
Linder JA, Schnipper JL, Middleton B. Method of electronic health record documentation and quality of primary care. J Am Med Inform Assoc. 2012 Nov-Dec;19(6):1019-24. doi: 10.1136/amiajnl-2011-000788. Epub 2012 May 19.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
R01HS015169-1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.