Skip to main content
Clinical Trials/NCT01509222
NCT01509222CompletedNot Applicable

Changing Dietary Patterns: an Individually Tailored Nutrition Intervention

Wageningen University2 sites in 1 country186 target enrollmentStarted: September 2011Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
186
Locations
2
Primary Endpoint
Changes in dietary pattern

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts 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.

Outcomes

Primary Outcomes

Changes in dietary pattern

Time Frame: baseline and 6 months

Dietary 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 Outcomes

  • Dietary behaviour(baseline and 6 months)
  • Health outcomes(baseline and 6 months)
  • Markers of intake(baseline and 6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lisette de Groot

(Hooft van Huysduynen)

Wageningen University

Study Sites (2)

Loading locations...

Similar Trials