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Instrument Design and Validation to Asses the Perception of Wellbeing Associated to Plain Water.

NCT01982981 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 142

Last updated 2013-11-13

No results posted yet for this study

Summary

Nowadays, it is common to ingest beverages other than plain water, which range from flavored with a low energy input to others of high input. In Mexico, flavored beverage ingestion is believed to be displacing plain water; this phenomenon is raising concern in the health sector, due to the relation between flavored beverage intake and the increase in obesity and, consequently, chronic diseases.

Up until now, there is no instrument available to characterize the perception of the Mexican population's well-being, beliefs and knowledge regarding plain water ingestion, nor is there an instrument capable of quantifying the daily water ingestion.

The purpose of this study is design and validate a questionnaire to identify and evaluate the perception of well-being (PWBQ) related to plain water consumption in a sample of adult men and women of the city of Cuernavaca.

Conditions

  • Wellbeing

Interventions

OTHER

water provision

perception behavioral change at the beginning and at the end of the intervention

OTHER

Water provision

After participants are recruited, drink 2L of water for 8 weeks.

Sponsors & Collaborators

  • Mexican National Institute of Public Health

    lead OTHER_GOV

Principal Investigators

  • Simón Barquera, PhD · Mexican National Institute of Public Health

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
59 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2012-10-31
Completion
2012-12-31

Countries

  • Mexico

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01982981 on ClinicalTrials.gov