Effectiveness of Primary Care Physicians in Delivering Weight Control Counseling

Obesity Clinical Trial

Official title:

Treatment of Obesity in the Primary Care Setting

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00017706
• Other study ID #: Simkin-Silverman (completed)
• Secondary ID: DK52050
• Status: Completed
• Phase: N/A
• First received: June 7, 2001
• Last updated: January 12, 2010
• Est. completion date: May 2001

Study information

• Verified date: January 2010
• Source: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

This randomized clinical trial will determine the efficacy of physicians providing weight control advice to their overweight and obese patients in primary care practice.

Description:

Enrolled physicians are randomly assigned to receive brief training in either: 1) behavioral weight control intervention or 2) obesity education. Enrolled patients are asked to see their physician for 2 weight control consultations during the year to discuss their weight and physical activity. Regardless of the training the physician receives, the weight control advice is tailored to the individual patient. Patients include men and women between the ages of 21 - 70 years, with a Body-Mass Index of 27 or greater, and they have met medical and other study eligibility criteria in order to safely participate. As a participant in the trial, all patients are asked to attend an initial baseline assessment, and two follow-up assessments; 3 and 12 months after their first weight control consultation visit with their physician in order to evaluate any changes in their weight, waist circumference, physical activity, eating patterns, and mood. The findings of this important study will shed light upon the role physician advice may have in helping overweight and obese patients lose weight and become more physically active.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Est. completion date: May 2001
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 21 Years to 70 Years

Eligibility

Inclusion Criteria:

• Body-Mass Index greater than or equal to 27

• Able to walk without assistance

• No untreated hypothyroidism or Cushing Disease

• No unstable medical or psychiatric condition

• No signs or symptoms of cardiovascular disease

• No history of gallstones

• No terminal illness

• No other acute or chronic medical condition in which weight loss is contraindicated

• Medically cleared for physical activity

Exclusion Criteria:

• Pregnant, nursing or planning to become pregnant in the next year

• Had an in-patient hospital stay in the last 3 months

• Lost more than 10 lbs in the last 4 months

• Taking an OTC or prescribed medication for weight loss

• In treatment for an eating disorder

• In treatment for depression (if patient is on an anti-depressant and has not had a recent episode of depression in the past 3 months then he/she is eligible)

Study Design

Allocation: Randomized, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Obesity

Intervention

Behavioral:
• physician-delivered weight control

Locations

Country	Name	City	State
United States	University of Pittsburgh, GSPH	Pittsburgh	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Simkin-Silverman LR, Wing RR. Management of obesity in primary care. Obes Res. 1997 Nov;5(6):603-12. — View Citation