Status:

COMPLETED

Evaluation of the Remote Intervention for Diet and Exercise (RIDE)

Lead Sponsor:

Pennington Biomedical Research Center

Collaborating Sponsors:

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

Conditions:

Overweight

Obesity

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

A large proportion of the adult population in the United States qualifies for weight loss treatment based on the NIH treatment recommendations, but traditional clinic-based weight loss treatments have...

Detailed Description

The prevalence of overweight and obesity has increased significantly over the past four decades, resulting in 66% of the adult population in the United States (U.S.) being classified as overweight or ...

Eligibility Criteria

Inclusion

  • Body mass index (BMI) is \> 25 kg/m2 and \< 35 kg/m2.
  • Willing to use cell phones provided by the PBRC or personal cell phones to take pictures of foods during the study and to receive messages from study personnel.
  • Willing to wear an activity monitor on your shoe and to use the internet to send information as frequently as once daily.
  • Willing to weigh on a scale provided by the PBRC as frequently as once per day
  • Willing to accept random assignment to either the e-Health (RIDE group) or control group.
  • Weight stable, defined as no greater than 4.4 lbs. (2 kg) weight change over the previous 60 days.

Exclusion

  • Diagnosed with a chronic disease that affects body weight, appetite, or metabolism, namely diabetes, cardiovascular disease, cancer, and thyroid diseases or conditions.
  • Currently in a weight loss program.
  • Unable to engage in moderate intensity exercise.
  • Unable to diet or exercise due to your medical history or current health status.
  • Current use of prescriptions or over-the-counter medications or herbal products that affect appetite, body weight, or metabolism (e.g., weight loss medications such as sibutramine, antipsychotic medications such as olanzapine, ephedrine, and diuretics).
  • Diagnosed with uncontrolled hypertension (high blood pressure), defined as systolic blood pressure \>159 mmHg \& diastolic blood pressure \>99 mmHg.
  • For females, current pregnancy, or plans to become pregnant in the duration of the study.

Key Trial Info

Start Date :

May 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

January 1 2011

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT00883350

Start Date

May 1 2009

End Date

January 1 2011

Last Update

December 3 2024

Active Locations (1)

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Pennington Biomedical Research Center

Baton Rouge, Louisiana, United States, 70808