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Effectiveness of Brief Counseling for Weight Management

Information source: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Information obtained from ClinicalTrials.gov on June 20, 2008
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: 1. Obesity

Intervention: orlistat (Drug); Brief cognitive behavioral counseling (Behavioral)

Phase: Phase 4

Status: Completed

Sponsored by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Official(s) and/or principal investigator(s):
John P Foreyt, PhD, Principal Investigator, Affiliation: Baylor College of Medicine

Summary

The purpose of this study is to test the effectiveness of three different methods for delivering weight management information. Two methods utilize an obesity drug and the third method utilizes brief behavioral counseling sessions only.

Clinical Details

Official title: Effectiveness of Brief Counseling for Weight Management

Study design: Treatment, Randomized, Open Label, Uncontrolled, Parallel Assignment, Efficacy Study

Primary outcome:

1. Changes in body weight at 6, 12 and 24 months.

2. Changes in body mass index (BMI) at 6, 12 and 24 months.

Secondary outcome:

1. Changes in blood pressure at 6, 12 and 24 months.

2. Changes in lipids at 6, 12 and 24 months.

3. Changes in serum glucose at 6, 12 and 24 months.

Detailed description: There is a growing demand for effective obesity treatments that don't require much time to implement especially in a primary health-care setting where time is especially limited. Brief interventions that might provide benefits similar to those produced by more time-intensive and costly lifestyle interventions would be very useful. There is also increasing interest in the efficacy of primary drug therapies for obesity. The purpose of this 12-month study, and 24-month follow-up, is to examine the efficacy of a brief behavioral counseling intervention alone or in combination with a drug already approved for the long-term management of obesity (orlisat)and compare both interventions to a drug alone condition.

Eligibility

Minimum age: 25 Years. Maximum age: 55 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Body Mass Index of 30 to 40

- Male or females ages of 25 to 55 years

- Normal blood pressure or controlled with medicine

- Females not lactating, able to get pregnant or using acceptable birth control

- Current allowed medications prescribed at least 2 months prior to study

Exclusion Criteria:

- Pregnant, planning to get pregnant or becomes pregnant

- Insulin dependent diabetes

- Uncontrolled hypertension

- Prescence or history of significant medical conditions that could impact the outcome

of the study

- Prescence of active gastrointestinal disorders

- History of mental disorders including eating disorders

- Weight loss greater than 10 pounds in the last 3 months

- History of alcohol or drug dependency

- Use of any weight-loss medication in the last 6 months

- Known allery to orlistat or any of its components

Locations and Contacts

Baylor College of Medicine, Houston, Texas 77030, United States
Additional Information

Starting date: January 2002
Ending date: August 2004
Last updated: December 14, 2007

Page last updated: June 20, 2008

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