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Clinical Trials/NCT00119964
NCT00119964
Completed
Phase 1

Weight Management for a Defined Employee Population Using an Interactive eHealth Portal

Robert Wood Johnson Foundation1 site in 1 country500 target enrollmentSeptember 2004
ConditionsObesity

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Obesity
Sponsor
Robert Wood Johnson Foundation
Enrollment
500
Locations
1
Primary Endpoint
change in body mass index
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to determine if an internet-based intervention will be effective in improving the lifestyle and weight of an obese employee population.

The intervention will last 12 months, and includes a weight tracker, a food intake tracker, an activity tracker, a calorie balance tool, an electronic discussion board, and electronic greeting cards.

Detailed Description

The study will compare two groups over time, one of which will utilize the electronic tools, and one of which will not. The samples will be drawn from the employees of a metro-Milwaukee hospital, and will consist of obese (Body Mass Index, or BMI, of 30 or greater) employees only. The primary outcome will be change in weight over the study time period as measured by the BMI. Secondary outcome measures will include quality of life, blood pressure, tests of blood sugar, cholesterol, presence of depression, lifestyle wellness score, health care costs and productivity.

Registry
clinicaltrials.gov
Start Date
September 2004
End Date
August 2007
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Robert Wood Johnson Foundation

Eligibility Criteria

Inclusion Criteria

  • Obesity as defined by a BMI of 30 or greater
  • The ability to speak and understand english
  • Health insurance coverage through First Health (Aurora's employee insurance plan)
  • Not currently on another formal weight management program
  • Not currently taking any weight loss medications
  • Not currently disabled in such a way that participation would be precluded

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

change in body mass index

Secondary Outcomes

  • hemoglobin A1c
  • total cholesterol
  • HDL cholesterol
  • HANDS depression score
  • wellness score on Summex Health Risk Appraisal
  • health care costs
  • unscheduled paid time off
  • quality of life
  • blood pressure

Study Sites (1)

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