Obesity Assessment and Education Through the Internet
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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 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label |
| Official Title: | Obesity Assessment and Education Through the Internet |
- Physician counseling about weight and weight-related behaviors
- 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 |
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 |
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| United States, Massachusetts | |
| Beth Israel Deaconess Medical Center | |
| Boston, Massachusetts, United States, 02215 | |
| Principal Investigator: | Christina C. Wee, MD, MPH | Beth Israel Deaconess Medical Center |
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00149682 History of Changes |
| Other Study ID Numbers: | OAEI (completed) |
| Study First Received: | September 6, 2005 |
| Last Updated: | January 12, 2010 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK):
|
Obesity |
Additional relevant MeSH terms:
|
Obesity Overnutrition Nutrition Disorders |
Overweight Body Weight Signs and Symptoms |
ClinicalTrials.gov processed this record on May 19, 2013