View Clinical Trial (Medical Research Study)
Pediatric Quality of Life Among Population With BMI Greater Than or Equal to 85%: Impact of a Behavioral Intervention Program
| City: |
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Brighton |
| State: |
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Massachusetts |
| Zip Code: |
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02135 |
| Conditions: |
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Pediatric Obesity |
| Purpose: |
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We are currently experiencing an epidemic of obesity in the Pediatric Population. This
epidemic affects many areas including quality of life.
We have been conducting a nutrition and exercise program since 2003. We have noticed that
many of the participants seem to have a better quality of life after finishing the one year
program compared to when they started. We would like to objectively quantify this
improvement using a validated questionnaire at the beginning and at the end of the study.
Questionnaires will be given to participants and to their caretakers at the same time.
There will be two groups in the study: one intervention (minimum attendance of 4 sessions)
and one control group.
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| Study Summary: |
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We are currently experiencing an obesity epidemic in the Pediatric population. The latest
NHANES data indicates that 16.5% has a BMI greater than or equal to 85% < 95% and 17.1% has
a BMI greater than or equal to 95%. The quality of life of children who are obese has been
shown to be lower than that of children with cancer. Health related quality of life
measurements have emerged as an important health outcome in clinical trials, clinical
practice improvement strategies, and healthcare services research and evaluation. We have
conducted a behavioral nutrition and exercise program since 2003. The name of the program
is the TEEEN (teens, empowerment, exercise, education, nutrition). We meet once a month on a
Saturday afternoon for four hours. During this time we cover: registration (monitoring of
sedentary activities and liquid choices; motivational interview, exercise testing);
exercise; educational interactive lectures; didactic games and projects. We have noticed
that participants seem to have a better quality of life after participating in the program
compared to baseline. We would like to objectively quantify this subjective finding. We
will be using the PedsQL(TM)4.0 questionnaire which has been validated in the pediatric
population. We will have an intervention and a control group. Both participants and their
caretakers will be given a questionnaire at the beginning and at the end of the study.
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| Criteria: |
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Inclusion Criteria:
- Ages 10-20
- BMI greater or equal to 85%
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| NCT ID: |
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NCT00714870 |
| Primary Contact: |
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Principal Investigator
Shirley Gonzalez, MD
Steward St. Elizabeth's Medical Center
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| Backup Contact: |
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N/A |
| Location Contact: |
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Brighton, Massachusetts 02135
United States
Shirley Gonzalez, MD
Phone: 617-926-0114
Email: shirleyg2008@gmail.com
Site Status: Recruiting |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 19, 2013 |
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