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HealtheTech Lifestyle Program

This study has been completed.
ClinicalTrials.gov Identifier:
First Posted: September 7, 2005
Last Update Posted: March 13, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
The Cooper Institute
The purpose of the study is to determine the efficacy of resting metabolic rate (RMR) using BodyGem and BalanceLog in helping overweight and obese individuals manage their weight.

Condition Intervention Phase
Obesity Behavioral: HealtheLifestyle Program Behavioral: step counters with monthly feedback on logs Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Single
Official Title: HealtheLifestyle Behavioral Intervention Clinical Trial

Further study details as provided by The Cooper Institute:

Primary Outcome Measures:
  • HealtheLifestyle participants will have greater weight loss

Secondary Outcome Measures:
  • HealtheLifestyle Program will increase efficacy of products

Estimated Enrollment: 130
Study Start Date: March 2004
Estimated Study Completion Date: February 2006
Detailed Description:
The study plans are to develop and test the efficacy of a practical, structured, and time-limited behavioral intervention (HealtheLifestyle Program) as a supplement to standard HealtheTech products. Approximately 130 participants will be recruited and randomized to either the HealtheTech Program (focusing on calorie and exercise goals using the BalanceLog for tracking), the HealtheLifestyle Program (using step counters, monthly email letters and calls providing information on activity, nutrition, and weight loss), or a delayed treatment program (after 3 months undergo the intervention above).

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria: healthy adult men and women, 18-60 years -

Exclusion Criteria: not currently participating in a structured diet or exercise program

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00146510

United States, Texas
The Cooper Institute
Dallas, Texas, United States, 75230
Sponsors and Collaborators
The Cooper Institute
Study Director: Heather Kitzman, MPH The Cooper Institute
  More Information

ClinicalTrials.gov Identifier: NCT00146510     History of Changes
Other Study ID Numbers: CI-0126
First Submitted: September 2, 2005
First Posted: September 7, 2005
Last Update Posted: March 13, 2014
Last Verified: March 2014

Keywords provided by The Cooper Institute:
weight control
physical activity
Health Behavior
Patient Compliance