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Obesity Assessment and Education Through the Internet
This study has been completed.
Sponsored by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Information provided by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ClinicalTrials.gov Identifier: NCT00149682
  Purpose

The purpose of this study is to develop a web-based obesity risk assessment and counseling tool and examine its feasibility and effectiveness in improving the rate and quality of physician counseling about obesity, dietary change, and physical activity.


Condition Intervention Phase
Obesity
Behavioral: 6-month educational program
Behavioral: 6-month standard care program
Phase II

MedlinePlus related topics: Obesity
U.S. FDA Resources
Study Type: Interventional
Study Design: Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: Obesity Assessment and Education Through the Internet

Further study details as provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK):

Primary Outcome Measures:
  • Physician counseling about weight and weight-related behaviors

Secondary Outcome Measures:
  • Changes in cardiovascular risk factors
  • Improvements in physical activity and dietary behavior

Estimated Enrollment: 100
Study Start Date: July 2005
Estimated Study Completion Date: December 2007
Detailed Description:

Despite the high prevalence of obesity and its associated health risks, physicians do not address weight and behaviors that contribute to obesity because of lack of knowledge, training, and access to resources. To address these physician barriers to counseling, the investigator has developed a web-based tool that collects and integrates relevant patient clinical and behavioral information online and generates patient-specific recommendations and links to resources in the form of electronic patient and physician reports. In doing so, the tool provides physicians with a time saving device that identifies at risk patients who are motivated to make behavioral changes; at the same time, the tool provides tailored resources and recommendations that help physicians deliver more effective counseling.

The pilot study described in this application randomizes overweight primary care patients to a control group and the web-based intervention. The aims of the study are to examine the feasibility of incorporating the web-based tool into primary care practice and to collect preliminary data on its potential effectiveness on improving the rate and quality of physician-patient discussions about weight and on improving several clinical and behavioral outcomes.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Received invitation from participating primary care practices
  • Scheduled non-urgent appointment with their usual primary care provider
  • BMI > 25 kg/m2
  • Willing and able to participate in a web-based computerized self-administered questionnaire
  • English-speaking

Exclusion Criteria:

  • Pregnancy
  • Terminal illness
  • Not competent to give consent
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00149682

Locations
United States, Massachusetts
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States, 02215
Sponsors and Collaborators
Investigators
Principal Investigator: Christina C. Wee, MD, MPH Beth Israel Deaconess Medical Center
  More Information

Publications:
Study ID Numbers: OAEI
Study First Received: September 6, 2005
Last Updated: July 31, 2007
ClinicalTrials.gov Identifier: NCT00149682  
Health Authority: United States: Federal Government

Keywords provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK):
Obesity

Study placed in the following topic categories:
Body Weight
Signs and Symptoms
Obesity
Nutrition Disorders
Overweight
Overnutrition

ClinicalTrials.gov processed this record on January 16, 2009