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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01023126
Other study ID # 972833
Secondary ID
Status Completed
Phase N/A
First received December 1, 2009
Last updated December 1, 2009
Start date May 2007
Est. completion date September 2009

Study information

Verified date December 2009
Source Feevale
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

Adherence to obesity treatment programs has been a limiting factor to good results in loosing weight. This study aimed to verify if obese subjects submitted to a physical exercise program and group psychotherapy would have a greater adherence, than obese people exercising only.


Description:

The sample was forty people, both genders, mean age: 42,2 ± 10,7 years old. Physical exercise consisted of walking and stretching three times a week, during 50 minutes, with intensity verified by the Borg Scale, during three months. One of the days were supervised by the authors while two were freely chosen by the participant, without supervision. The verified variables were: total body mass, height, body mass index, physical activity level, caloric expenditure, waist circumference and fat percentile. Half of the sample participated of group psychotherapy once weekly.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date September 2009
Est. primary completion date August 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 25 Years to 62 Years
Eligibility Inclusion Criteria:

- BMI >= 30 kg/m2

Exclusion Criteria:

- Age less than 25 or more than 62

Study Design

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


Related Conditions & MeSH terms


Intervention

Behavioral:
Group Psychotherapy
Group psychotherapy once a week, under a psychiatrist supervision

Locations

Country Name City State
Brazil Centro Universirário Feevale Novo Hamburgo RS

Sponsors (1)

Lead Sponsor Collaborator
Feevale

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Weight loose three months No
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