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Clinical Trials/NCT03250858
NCT03250858
Completed
N/A

Randomized Control Trial to Evaluate the Effectiveness of Online Nutrition Advice in the UK (The EatWellUK Study)

University of Reading1 site in 1 country324 target enrollmentAugust 15, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Dietary Modification
Sponsor
University of Reading
Enrollment
324
Locations
1
Primary Endpoint
Dietary intake
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The EatWellUK study aims to investigate the effectiveness of a mobile web application (e-Nutri), capable of delivering automated personalised nutrition advice, in increasing diet quality.

Dietary assessment is via the validated Food4Me FFQ (with an updated user interface that has been designed for better usability) and dietary feedback is derived according to adherence to an 11-item modified US Alternative Healthy Eating Index (m-AHEI).

Registry
clinicaltrials.gov
Start Date
August 15, 2017
End Date
January 30, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Julie Lovegrove

Professor

University of Reading

Eligibility Criteria

Inclusion Criteria

  • aged \> 18 years old

Exclusion Criteria

  • aged \< 18 years old
  • not living in the UK
  • pregnant/lactating
  • no or limited access to internet
  • following a prescribed diet for any reason
  • intolerance or food allergy
  • subject with diabetes, or any other metabolic disorder or illness that alters nutritional requirements

Outcomes

Primary Outcomes

Dietary intake

Time Frame: baseline, 6 weeks, 12 weeks

Change from baseline in dietary intake at 6 and 12 weeks assessed via a Food Frequency Questionnaire (FFQ). An 11-item modified US Alternative Healthy Eating Index (m-AHEI), which is calculated from the results of the FFQ, will be used to quantify the dietary intake changes.

Secondary Outcomes

  • Weight(baseline, 6 weeks, 12 weeks)
  • Physical activity(baseline, 6 weeks, 12 weeks)

Study Sites (1)

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