The Healthy Lifestyle Study
Weight Management for a Defined Employee Population Using an Interactive eHealth Portal
1 other identifier
interventional
500
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_1 obesity
Started Sep 2004
Longer than P75 for phase_1 obesity
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2004
CompletedFirst Submitted
Initial submission to the registry
July 6, 2005
CompletedFirst Posted
Study publicly available on registry
July 14, 2005
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2007
CompletedJuly 27, 2011
July 1, 2011
July 6, 2005
July 25, 2011
Conditions
Outcome Measures
Primary Outcomes (1)
change in body mass index
Secondary Outcomes (9)
quality of life
blood pressure
hemoglobin A1c
total cholesterol
HDL cholesterol
- +4 more secondary outcomes
Interventions
Eligibility Criteria
You may qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Aurora Health Care
Milwaukee, Wisconsin, 53215, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Alison Lux, MD
Wake Forest University Health Sciences
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- RANDOMIZED
- Masking
- NONE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
July 6, 2005
First Posted
July 14, 2005
Study Start
September 1, 2004
Study Completion
August 1, 2007
Last Updated
July 27, 2011
Record last verified: 2011-07