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The Relationship of TV Viewing to Energy Balance in Adults (TView)

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ClinicalTrials.gov Identifier: NCT00622050
Recruitment Status : Completed
First Posted : February 22, 2008
Last Update Posted : October 16, 2008
United States Department of Agriculture (USDA)
Information provided by:
University of Vermont

Brief Summary:

The specific objectives of this project are to:

  1. Investigate the effects of reducing TV viewing time on energy intake, eating behavior, and energy expenditure in overweight or obese adult subjects, thus providing a basis for evaluating if reducing TV viewing time might be a useful adjunct therapy in obesity prevention and treatment
  2. Analyze the types of foods eaten in conjunction with TV viewing
  3. Determine if there is an association between location of TV and BMI.

Condition or disease Intervention/treatment Phase
Obesity Overweight Behavioral: No TV viewing reduction Behavioral: TV viewing reduction Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 44 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Investigator)
Primary Purpose: Treatment
Official Title: The Effects of Limiting TV Viewing on Diet, Exercise, and Sleep in Overweight and Obese Adults
Study Start Date : January 2008
Actual Primary Completion Date : August 2008
Actual Study Completion Date : August 2008

Arm Intervention/treatment
Experimental: 1
This arm will be experiencing the same protocol as the control group, only their TV viewing time will be reduced. The TV viewing time reduction is the experimental intervention.
Behavioral: TV viewing reduction
In the experimental arm, TV viewing time will be reduced for half of the study protocol time (3-4 weeks of a 6-8 week protocol).

Active Comparator: Control
The control group will be experiencing the exact protocol; only their TV viewing time will not be reduced.
Behavioral: No TV viewing reduction
In the control group, no intervention will be acted upon. This group will receive the exact same protocol as the intervention group, but with observation only.

Primary Outcome Measures :
  1. Energy Intake [ Time Frame: Phase I and Phase II ]

Secondary Outcome Measures :
  1. Energy expenditure [ Time Frame: Phase I and Phase II ]

Information from the National Library of Medicine

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Ages Eligible for Study:   21 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • BMI between 25-50
  • Watch at least 3 hours of TV per day or 21 hours per week.
  • Between the ages of 21-65 years.
  • Willing to have study staff enter home several times.
  • Willing to have TV viewing time reduced.

Exclusion Criteria:

  • Live greater than 45 minutes from UVM campus.
  • Enrolled in a weight loss study
  • Pregnant or planning to become pregnant during active study protocol.
  • Breastfeeding for 6 months or less.

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): NCT00622050

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United States, Vermont
UVM Department of Nutrition and Food Sciences
Burlington, Vermont, United States, 05405
Sponsors and Collaborators
University of Vermont
United States Department of Agriculture (USDA)
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Jean Harvey-Berino/ Chair, Department of Nutrition and Food Sciences, Universtiy of Vermont
ClinicalTrials.gov Identifier: NCT00622050    
Other Study ID Numbers: CHRBS 08-052
First Posted: February 22, 2008    Key Record Dates
Last Update Posted: October 16, 2008
Last Verified: October 2008
Additional relevant MeSH terms:
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Body Weight