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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00622050
Other study ID # CHRBS 08-052
Secondary ID
Status Completed
Phase N/A
First received February 12, 2008
Last updated October 15, 2008
Start date January 2008
Est. completion date August 2008

Study information

Verified date October 2008
Source University of Vermont
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 21 Years to 65 Years
Eligibility 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.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

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.
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).

Locations

Country Name City State
United States UVM Department of Nutrition and Food Sciences Burlington Vermont

Sponsors (2)

Lead Sponsor Collaborator
University of Vermont United States Department of Agriculture (USDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Energy Intake Phase I and Phase II No
Secondary Energy expenditure Phase I and Phase II No
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