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Study to Evaluate the 'eNutri' Online Personalised Nutrition App in the United Kingdom (UK)

NCT03897972 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 216

Last updated 2019-11-29

No results posted yet for this study

Summary

The proof-of-principle EatWellEUR pilot study will investigate whether online personalised dietary advice encourages greater dietary behaviour change after 12 weeks compared with general population-based diet advice. Dietary change will be quantified from an 11-item diet quality score (DQS) suitable for Northern European populations that is calculated from the results of the eNutri food frequency questionnaire (FFQ) at baseline and week 12.

Conditions

  • Dietary Modification
  • Dietary Habits

Interventions

BEHAVIORAL

Non-personalised diet advice delivered via the eNutri app (control)

Non-personalised dietary advice to improve food choices based on standard population guidelines delivered by the eNutri app and irrespective of the dietary intakes from the food frequency questionnaire (control group).

BEHAVIORAL

Personalised diet advice delivered via the eNutri app (intervention)

Personalised dietary advice to improve food choices based on adherence to an 11-item diet quality score, which is determined by the eNutri app in response to the dietary intakes from the food frequency questionnaire (intervention group).

Sponsors & Collaborators

  • University of Reading

    lead OTHER

Principal Investigators

  • Julie Lovegrove, Professor · Hugh Sinclair Unit of Human Nutrition

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-08-05
Primary Completion
2019-12-31
Completion
2019-12-31

Countries

  • United Kingdom

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 NCT03897972 on ClinicalTrials.gov