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Electronic Tools to Assist With Identification of and Counseling for Overweight Patients

Primary Purpose

Overweight

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Electronic tool set for counseling overweight patients
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Overweight focused on measuring Overweight, Diagnosis, Counseling, Medical Records Systems, Computerized

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria (physicians):

  • Consenting physicians from the Northwestern Memorial General Internal Medicine (NMFF GIM) practice

Exclusion Criteria (physicians):

  • Study investigators will be excluded from participation (Dr. David Baker, Dr. Joyce Tang)

Inclusion Criteria (patients):

  • 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

Exclusion Criteria (patients):

  • 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.

Sites / Locations

  • Northwestern Memorial Faculty Foundation General Internal Medicine Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Electronic tools

Usual care

Arm Description

Outcomes

Primary Outcome Measures

Documented diagnosis of overweight

Secondary Outcome Measures

Documented counseling for overweight.
Documentation of specific behavior change goals

Full Information

First Posted
September 8, 2009
Last Updated
July 26, 2011
Sponsor
Northwestern University
Collaborators
Agency for Healthcare Research and Quality (AHRQ)
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1. Study Identification

Unique Protocol Identification Number
NCT00973661
Brief Title
Electronic Tools to Assist With Identification of and Counseling for Overweight Patients
Official Title
Electronic Tools to Assist With Identification of and Counseling for Overweight Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2011
Overall Recruitment Status
Completed
Study Start Date
March 2010 (undefined)
Primary Completion Date
September 2010 (Actual)
Study Completion Date
September 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Northwestern University
Collaborators
Agency for Healthcare Research and Quality (AHRQ)

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.
Detailed Description
Overweight adults (Body Mass Index [BMI] 25-29.9) are at high risk for developing obesity, but rates of physician identification and counseling of overweight adults are low. Alerts and tools embedded in the electronic medical record have shown promise in enhancing quality improvement efforts. Our aim is to design and assess the impact of an electronic alert and tool set to assist with identification and counseling of overweight patients with a BMI 27-29.9. Although the category of overweight patients spans BMI 25-29.9, we are including only patients with BMI 27-29.9 in order to focus resources on the most at-risk pre-obese population. We will develop a tool set including 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 in the Northwestern Memorial Faculty Foundation General Internal Medicine (NMFF GIM) practice who consent to participate in the study will be randomized into two groups, with one group of physicians receiving access to these tools. The other group of physicians will continue to provide their usual care for overweight patients. Outcome measures will include the following: tool usage; documentation of overweight in the problem list, encounter diagnosis, or note text; counseling for overweight and documentation of specific behavioral goals. Measures will be obtained via retrospective chart review.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight
Keywords
Overweight, Diagnosis, Counseling, Medical Records Systems, Computerized

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Electronic tools
Arm Type
Experimental
Arm Title
Usual care
Arm Type
No Intervention
Intervention Type
Behavioral
Intervention Name(s)
Electronic tool set for counseling overweight patients
Intervention Description
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.
Primary Outcome Measure Information:
Title
Documented diagnosis of overweight
Time Frame
September 1, 2009-February 28, 2010
Secondary Outcome Measure Information:
Title
Documented counseling for overweight.
Time Frame
September 1, 2009-February 28, 2010
Title
Documentation of specific behavior change goals
Time Frame
September 1, 2009-February 28, 2010

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria (physicians): Consenting physicians from the Northwestern Memorial General Internal Medicine (NMFF GIM) practice Exclusion Criteria (physicians): Study investigators will be excluded from participation (Dr. David Baker, Dr. Joyce Tang) Inclusion Criteria (patients): 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 Exclusion Criteria (patients): 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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joyce W Tang, MD
Organizational Affiliation
Northwestern University, Department of General Internal Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern Memorial Faculty Foundation General Internal Medicine Clinic
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States

12. IPD Sharing Statement

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