A Study of the Effect of Replacing Sugary Drinks by Low-sugar Alternatives on Body Weight and Fat Mass in Children (DRINK)

June 13, 2012 updated by: Margreet R. Olthof, VU University of Amsterdam

A Double-blind, Randomized Trial of the Efficacy of Replacing Sugary Drinks by Low-sugar Alternatives on Body Weight and Fat Mass in School Children

Obesity results from an imbalance between energy intake and energy expenditure. There is much speculation about foods that are particularly fattening, and sugary drinks are seen as major culprits. It is hypothesized that a high intake of calories from sugary drinks would not be compensated for by reduced food intake at subsequent meals. As a result, body weight would increase. In this double-blind, long term, randomized controlled trial the effect of replacing sugar-containing beverages by low-sugar alternatives on body weight and fat mass in children will be investigated.

Study Overview

Detailed Description

Rationale: Liquid carbohydrates (including soft drinks as well as fruit juices) are thought to be less satiating then solid carbohydrates (e.g., bread or fruits). The hypothesis is that calories from sugary drinks might not be compensated for by eating less at subsequent meals and body weight would increase. In this way liquid carbohydrates might be one of the causes of becoming overweight and obesity. However, the evidence for a causal relation between sugary drinks and weight gain is inconclusive.

Objective: To test the effect of replacing sugar-containing beverages by beverages low in sugar on body weight and fat mass in children aged 5-10 years.

Study design: A double-blind, long term, randomized controlled trial.

Study population: Healthy school children in the age of 5-10 years old. We consider it unethical to encourage children to drink sugary drinks. Therefore children are only eligible if they already habitually consume 250 mL per day or more of sugary drinks.

Intervention: Six hundred healthy children (5-10 years) will be divided randomly into 2 groups. Group 1 (n=300) receives 250 mL per day of sugar-containing lemonade. Group 2 (n=300) receives 250 mL per day of lemonade low in sugar. The low-sugar drinks are sweetened with artificial sweeteners. The drinks will be consumed during the morning break during the weekdays at school and at home during weekends and holidays. The intervention period will be 18 months.

Before the main trial starts feasibility and logistics will be tested in a pilot study. The design of the pilot study will be a 2-month randomized controlled trial in approximately 80 school children aged 5-10 years.

Main study parameters/endpoints: The primary outcome of the study is children's body weight (body mass index, corrected for age). Secondary endpoints are waist circumference, skin folds and bioelectrical impedance. These outcomes will be measured four times during the study, at 0, 6, 12 and 18 months. As a secondary outcome we will also perform a sensory evaluation at 0, 6, 12 and 18 months and a questionnaire about dental health at 12 and 18 months.

Study Type

Interventional

Enrollment (Actual)

641

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Amsterdam, Netherlands, 1081 HV
        • VU University Amsterdam

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

5 years to 10 years (CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Healthy school boys and girls
  • Age 5 years and older, children still have to be in elementary school at the end of the study
  • Children who already habitually consume 250 mL per day or more of sugary drinks

Exclusion Criteria:

  • Using medication or under medical treatment for obesity
  • Any acute or chronic disease such as diabetes, growth disorders, celiac disease, or serious gastroenterological diseases
  • Medical history or surgical events known to interfere with the study
  • Participation in another intervention trial up to 3 months before and during the study, if the intervention interferes with the current study
  • Physical disabilities that hamper the measurements
  • Intention to change location of residence and primary school during the study period

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: TRIPLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: dietary intervention 1
250 milliliters of lemonade with sugar daily for 18 months
EXPERIMENTAL: dietary intervention 2
250 milliliters of lemonade low in sugar daily for 18 months

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Body Mass Index Z-score
Time Frame: 0, 6, 12, and 18 months
0, 6, 12, and 18 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Skinfolds
Time Frame: 0, 6, 12 and 18 months
0, 6, 12 and 18 months
Waist to height ratio
Time Frame: 0, 6, 12 and 18 months
0, 6, 12 and 18 months
Bioelectrical Impedance
Time Frame: 0, 6, 12 and 18 months
% fat mass
0, 6, 12 and 18 months
Dental health
Time Frame: 12 and 18 months
12 and 18 months
Sensory evaluation
Time Frame: 0, 6 ,12 and 18 months

We perform a sensory evaluation, to relate the effects at the end of the trial to properties of our drinks, asking:

  1. How much do you want to drink the study drink?
  2. How satiated do you feel?
  3. What do you eat together with the study drink?
  4. How much do you like the study drink?

The questionnaire includes pictures, and was tested at baseline

0, 6 ,12 and 18 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Martijn B Katan, Prof. Dr., VU University of Amsterdam
  • Principal Investigator: Margreet R Olthof, Dr., VU University of Amsterdam

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2009

Primary Completion (ACTUAL)

July 1, 2011

Study Completion (ACTUAL)

July 1, 2011

Study Registration Dates

First Submitted

May 4, 2009

First Submitted That Met QC Criteria

May 4, 2009

First Posted (ESTIMATE)

May 6, 2009

Study Record Updates

Last Update Posted (ESTIMATE)

June 14, 2012

Last Update Submitted That Met QC Criteria

June 13, 2012

Last Verified

June 1, 2012

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ZONMW120520010-NHS2008B096

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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