Study to Evaluate the 'eNutri' Online Personalised Nutrition App in the United Kingdom (UK) (EatWellEUR)
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| ClinicalTrials.gov Identifier: NCT03897972 |
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Recruitment Status : Unknown
Verified November 2019 by Julie Lovegrove, University of Reading.
Recruitment status was: Active, not recruiting
First Posted : April 1, 2019
Last Update Posted : November 29, 2019
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Dietary Modification Dietary Habits | Behavioral: Non-personalised diet advice delivered via the eNutri app (control) Behavioral: Personalised diet advice delivered via the eNutri app (intervention) | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 216 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Participant) |
| Primary Purpose: | Prevention |
| Official Title: | Proof-of-principle Pilot Study to Investigate Whether Online Personalised Dietary Advice Given by the eNutri Diet App Encourages Greater Dietary Behaviour Change Than General Advice in UK Adults After 12 Weeks |
| Actual Study Start Date : | August 5, 2019 |
| Estimated Primary Completion Date : | December 2019 |
| Estimated Study Completion Date : | December 2019 |
| Arm | Intervention/treatment |
|---|---|
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Active Comparator: Non-personalised general diet advice
Control group to receive non-personalised dietary advice based on general public health dietary recommendations for Northern Europe. Advice will be delivered to the participant via the eNutri web application.
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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). |
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Experimental: Personalised diet advice
Intervention group to receive personalised dietary advice generated by the eNutri app from their actual dietary intakes and tailored according to their body mass index and food preferences. Advice will be delivered to the participant via the eNutri app web application and will be generated based on their adherence to an 11-item diet quality score suitable for Northern European populations.
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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). |
- eNutri diet quality score (DQS) [ Time Frame: Baseline & week 12 ]Dietary intake at baseline and week 12 will be assessed via the eNutri food frequency questionnaire (FFQ) from which an 11-item eNutri DQS will be calculated. The eNutri DQS was developed for Northern Europe and quantifies diet quality (i.e. the healthiness of a diet). It is composed of 11 food and nutrient components (contributing 10 points each) that are summed to give an overall score (between 0-110 points), where higher scores reflect the healthiest diets based on adherence to dietary recommendations.
- Body mass index (BMI) [ Time Frame: Baseline & week 12 ]Self reported measurements of weight and height will be used to determine BMI.
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Living in the UK
- Can understand written English
Exclusion Criteria:
- Food allergies or food intolerances (diagnosed or self-diagnosed)
- Receiving professional nutritional advice from a dietitian, nutritionist or medical professional
- Following a specialised diet (e.g. vegan, calorie-controlled/weight-loss diet)
- Athletes or those following a or sports nutrition regimen
- Pregnant, lactating or planning a pregnancy within the next 3 months
- Diagnosed medical conditions that require specific dietary guidance (e.g. diabetes, Crohn's disease or eating disorders), those who are currently undergoing rigorous medical treatment (e.g. chemotherapy for cancer) or conditions that affect memory (e.g. dementia)
- Medications that impact on diet (e.g. weight-loss medication) or involve dietary restrictions
- Those who eat less than 2 meals per day
- Excessive use of herbal or dietary supplements (e.g. 3 or more per day)
- Taking part in another nutrition study
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03897972
| United Kingdom | |
| Hugh Sinclair Unit of Human Nutrition, Department of Food and Nutritional Sciences, University of Reading | |
| Reading, Berkshire, United Kingdom, RG6 6AP | |
| Principal Investigator: | Julie Lovegrove, Professor | Hugh Sinclair Unit of Human Nutrition |
| Responsible Party: | Julie Lovegrove, Director of the Hugh Sinclair Unit of Human Nutrition, University of Reading |
| ClinicalTrials.gov Identifier: | NCT03897972 |
| Other Study ID Numbers: |
08/19 |
| First Posted: | April 1, 2019 Key Record Dates |
| Last Update Posted: | November 29, 2019 |
| Last Verified: | November 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Personalised nutrition |

