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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04463407
Other study ID # BIOEPUCV-H145-2017
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 28, 2017
Est. completion date September 28, 2017

Study information

Verified date July 2020
Source Pontificia Universidad Catolica de Valparaiso
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present study aimed to investigate the effects of a single nutritional preventive session previous to a critical period linked to fat gain in university students with overweight and obesity, emulating a nutritional session of a public health system.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date September 28, 2017
Est. primary completion date September 27, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Body mass index [BMI] =25 kg/m2

- Not having metal plates

- Not studying Nutrition and Dietetics or Physical Education

- Not being pregnant

Exclusion Criteria:

- Presente gastrointestinal problems (vomit or diarrheas) during the three weeks that last the experiment.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Educational talk about physical activity and nutritional recommendations before a critical period of fat gain in university students
An intervention was performed emulating a traditional nutritional session from a primary healthcare center (public health system). Traditionally, this session lasts around 20 minutes and includes a body composition measurement, nutritional assessment, and a brief educational talk about healthy eating. Just the intervention group received a series of healthy recommendations specially focused on the National Holiday.

Locations

Country Name City State
Chile School of Physical Education, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile Valparaíso Valparaiso

Sponsors (1)

Lead Sponsor Collaborator
Pontificia Universidad Catolica de Valparaiso

Country where clinical trial is conducted

Chile, 

Outcome

Type Measure Description Time frame Safety issue
Primary Body composition measurements Changes on fat mass measured by DXA 3 weeks
Secondary Feeding questionnaires and food guide recommendations Changes on the Global Food Index 3 weeks
Secondary Feeding questionnaires and food guide recommendations Changes on the KIDMED index (questionnaire establishes the adherence to the Mediterranean diet) 3 weeks
Secondary Feeding questionnaires and food guide recommendations Changes on the Food Guide Recommendation 3 weeks
Secondary Physical activity level Modification on physical activity level measured by accelerometry 3 weeks
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