HealtheTech Lifestyle Program

This study has been completed.
Sponsor:
Collaborator:
HealtheTech
Information provided by:
The Cooper Institute
ClinicalTrials.gov Identifier:
NCT00146510
First received: September 2, 2005
Last updated: March 12, 2014
Last verified: March 2014
  Purpose

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
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Single Blind
Official Title: HealtheLifestyle Behavioral Intervention Clinical Trial

Resource links provided by NLM:


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).

  Eligibility

Ages Eligible for Study:   18 Years to 60 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00146510

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

No publications provided

ClinicalTrials.gov Identifier: NCT00146510     History of Changes
Other Study ID Numbers: CI-0126
Study First Received: September 2, 2005
Last Updated: March 12, 2014
Health Authority: United States: Institutional Review Board

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

Additional relevant MeSH terms:
Obesity
Overnutrition
Nutrition Disorders
Overweight
Body Weight
Signs and Symptoms

ClinicalTrials.gov processed this record on August 20, 2014