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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01358773
Other study ID # #0135/04
Secondary ID
Status Recruiting
Phase Phase 0
First received December 3, 2010
Last updated June 29, 2016
Start date February 2004
Est. completion date December 2016

Study information

Verified date June 2016
Source Federal University of São Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

Obese adolescents are submitted to a multiprofessional weight loss program, which is formed by doctors, nutritionists, physiotherapists, psychologists,and physiologists. The volunteers have intervention 3 times a week during one year, where they practice exercises, have nutrition and psychology counseling, and physiotherapy orientation. Once a month they have an appointment with the doctor. The hypothesis of this study is that a multiprofessional therapy is able to improve anthropometric and biochemical parameters, and also the quality of life of obese adolescents.


Description:

The volunteers are submitted to 10 exams (electrocardiogram, polysomnography, blood collection, body composition, rest metabolic rate, DXA, abdominal and carotid ultrasonography, lung function evaluation, ergospirometric test) 3 times a year (baseline, middle and at the end of the year). They also answer nutrition, sleep and psychology questionnaires.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date December 2016
Est. primary completion date December 2004
Accepts healthy volunteers No
Gender Both
Age group 15 Years to 19 Years
Eligibility Inclusion Criteria:

- present obesity ( BMI > 95th)

- aged between 15-19 years old

- be able to practice exercise

Exclusion Criteria:

- pregnancy

- use of drugs

- secondary obesity

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
multidisciplinary intervention
Comparison of the polysomnography results, blood collection parameters, resting metabolic rate values, body composition variables, carotid artery thickness values, abdominal and subcutaneous fat and lung function variables baseline, middle and at the end of the one year of interdisciplinary weight loss program combined exercise training with physiotherapy, clinical, nutritional and psychological therapies.

Locations

Country Name City State
Brazil CEPE São Paulo SP

Sponsors (4)

Lead Sponsor Collaborator
Ana R. Damaso Ana Claudia Pelissari Kravchychyn, Raquel Munhoz da Silveira Campos, Sofia Emanuelle Castro

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Body composition The body composition was measured by plethysmography and by densitometry. six months Yes
Secondary visceral and subcutaneous fat were analyzed by ultrasound The visceral and subcutaneous fat were analyzed by ultrasound six months Yes
Secondary Serum analysis The serum analysis was done by blood samples that were collected at the outpatient clinic around 8 a.m. after an overnight fast by a skilled and qualified technician. six months Yes
Secondary Lung function The lung function was measured with a spirometer EasyOne® model 2001 (Zurich, CH) according to American Thoracic Society criteria. six months Yes
Secondary Arterial intima-media thickness The arterial intima-media thickness was measured by High-resolution ultrasound equipment with a 7-14 MHz linear array transducer. six months Yes
Secondary Sleep parameters The sleep parameters were evaluated by polysomnography and specific questionnaires. six months Yes
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