Electronic Tools to Assist With Identification of and Counseling for Overweight Patients
1 other identifier
interventional
2,600
1 country
1
Brief Summary
The purpose of this study is to design and assess the impact of an electronic alert and tool set to assist with physician identification and counseling of overweight patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2010
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
September 8, 2009
CompletedFirst Posted
Study publicly available on registry
September 9, 2009
CompletedStudy Start
First participant enrolled
March 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2010
CompletedJuly 27, 2011
July 1, 2011
6 months
September 8, 2009
July 26, 2011
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Documented diagnosis of overweight
September 1, 2009-February 28, 2010
Secondary Outcomes (2)
Documented counseling for overweight.
September 1, 2009-February 28, 2010
Documentation of specific behavior change goals
September 1, 2009-February 28, 2010
Study Arms (2)
Electronic tools
EXPERIMENTALUsual care
NO INTERVENTIONInterventions
Physicians randomized to the "electronic tools" arm will receive access to a tool set to aid with counseling of overweight patients. This tool set includes the following components: automatic calculation of BMI, alert for overweight status, counseling template for weight loss goal-setting, linkage to referral options, and access to relevant patient handouts. Physicians randomized to the "usual care" arm will not receive access to these tools, and will continue to provide their usual care for overweight patients.
Eligibility Criteria
You may qualify if:
- Consenting physicians from the Northwestern Memorial General Internal Medicine (NMFF GIM) practice
You may not qualify if:
- Study investigators will be excluded from participation (Dr. David Baker, Dr. Joyce Tang)
- Adults ages 18-65 seen at the NMFF GIM who are patients of consenting physicians
- Have at least one appointment at the NMFF GIM clinic between 9/1/09-2/28/10
- Body mass index (BMI) 27-29.9 at one or more visits between 9/1/09-2/28/10
- Patients without at least one recorded height measurement from any prior visit or without weight information from a visit within the 6 month target window will be excluded due to inability to calculate BMI.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Northwestern Memorial Faculty Foundation General Internal Medicine Clinic
Chicago, Illinois, 60611, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Joyce W Tang, MD
Northwestern University, Department of General Internal Medicine
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 8, 2009
First Posted
September 9, 2009
Study Start
March 1, 2010
Primary Completion
September 1, 2010
Study Completion
September 1, 2010
Last Updated
July 27, 2011
Record last verified: 2011-07