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OpenTrials
Completed

NCT Number: NCT00149682

Obesity Assessment and Education Through the Internet

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.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Beth Israel Deaconess Medical Center

Boston, Massachusetts, 02215, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

6-month educational program

Behavioral

6-month standard care program

Behavioral

Primary outcomes

  1. Physician counseling about weight and weight-related behaviors

Secondary outcomes

  1. Changes in cardiovascular risk factors

  2. Improvements in physical activity and dietary behavior

Sponsors and collaborators

Lead sponsor

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Nih

Registry information

Important dates

Study start
2005
Study completion
2007
First posted
Sep 8, 2005
Registry last updated
Jan 13, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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