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Changing Dietary Patterns: an Individually Tailored Nutrition Intervention (OKE-study)

Changing Dietary Patterns: an Individually Tailored Nutrition Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01509222
Enrollment
186
Registered
2012-01-12
Start date
2011-09-30
Completion date
2013-04-30
Last updated
2013-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Health promotion, Dietary Counseling

Brief summary

The main objective of this study is to investigate the effect of a personalized nutrition intervention on the dietary pattern of apparently healthy adults with one or more children aged 4 to 12 years.

Detailed description

Giving personalized nutrition advice is perceived to be more effective in changing dietary patterns than giving general information about healthy eating.

Interventions

BEHAVIORALPersonalized nutrition counseling

Sponsors

Wageningen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* At least aged 18 years * Having one child aged 4 to 12 years * Written informed concent has been obtained

Exclusion criteria

* Not meeting the inclusion criteria * Unable or unwilling to comply with the study procedures * Enrolled in another study during the same study period * Not being able to communicate (read, speak and write) in the Dutch language * Having a partner who has been enrolled in the study * Being pregnant or lactating during the study period or planning to become pregnant during the study period * Having a BMI lower than 18.5 or higher that 35 kg/m2 * Using medication to lower cholesterol or being under control by a doctor for having too high cholesterol levels * Using medication to lower blood pressure or being under control by a doctor for having a high blood pressure. * Having diabetes type I or type II * Following a diet (medical or self-initiated) or planning to follow a diet during the study period * Undergoing a medical treatment that interferes with the intervention. * Having gained or lost more than 5 kg of body weight during the last 6 months.

Design outcomes

Primary

MeasureTime frameDescription
Changes in dietary patternbaseline and 6 monthsDietary pattern will be measured by scoring several aspects of the diet. There are 10 aspets included in the score; fruit consumption, vegetable consumption, fiber intake, fatty acids intake, trans fatty acids intake, physical activity, consumption occasions, alcohol intake, fish consumption and sodium intake. The range of the score is from 0 to 100. The score will be based on the information of a Food Frequency Questionnaire and two 24 hour dietary recalls.

Secondary

MeasureTime frameDescription
Dietary behaviourbaseline and 6 monthsBehavioral factors influencing dietary intake like barriers for having a healthy diet.
Health outcomesbaseline and 6 monthsHealth outcome measure are; BMI, waist and hip circumference, blood lipids (cholesterol and triglycerides) and blood pressure
Markers of intakebaseline and 6 monthsBlood values of carotenoids and fish fatty acids will be used to assess whether measured changes in dietary pattern are also found in the blood. Urinary potassium and sodium ratios will also be used to assess changes in dietary pattern.

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026