MedPath

Usability of myfood24 in Clinical Populations

Early Phase 1
Completed
Conditions
Gastroenterology Surgery
Colorectal Surgery
Weight Loss
Weight Change, Body
Interventions
Other: usual care
Other: myfood24
Registration Number
NCT04758559
Lead Sponsor
University of Leeds
Brief Summary

Many patients would benefit from dietary/nutritional support to better manage their conditions but evaluating current intake in relation to personal targets is labour-intensive and often does not feature as part of clinical consultations.

Primary objective: test usability and acceptability of 'myfood24 Health' for monitoring dietary intake in a group of patients.

Recruit 60 gastroenterology surgery patient (Leeds) and 60 Tier 3 Weight Management patients (30 Leeds/ 30 York).

Randomise to 3 groups

1. usual care

2. myfood24Health

3. myfood24Health plus personalised feedback 'diet optimisation engine' which suggests changes to amounts or types of foods

During a 2-month follow-up, patients in group 2 or 3 will be asked to record daily diet in myfood24, including weekend and weekdays and use it a minimum of 4 times.

HCPs will be able to review diet/nutrients for group 2 and 3 patients and can support dietary change or nutritional goals, as part of patients' ongoing clinical management, during existing scheduled clinic visits (N.B. not all participants will have a scheduled clinic appointment during the study).

2 months after recruitment, all participants will receive a link to an online feedback questionnaire.

At end of study, HPCs will be invited to provide feedback during a 30 minute interview.

Detailed Description

See published results at https://www.mdpi.com/2072-6643/14/9/1768

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
48
Inclusion Criteria
  • Able to use a smartphone or tablet
  • Have regular access to the internet
  • Aged 18 years or over
  • Not receiving palliative treatment for their condition
  • No pre-existing condition, eg. diabetes which requires a specific diet or eating disorder
  • No food allergies
  • Be receiving ongoing gastrointestinal surgery or weight management treatment
  • Be able to read and understand English
Exclusion Criteria

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Usual careusual carePatients receive usual care concerning dietary advice.
myfood24myfood24Patients receive myfood24 a new online app to support tracking of food and nutrient intakes, and allows patients and healthcare professionals to communicate, seeing results of intakes to promote healthy dietary behaviour changes.
myfood24 + diet optimisationmyfood24Personalised feedback. Patients use myfood24 with an additional feature of new technology providing guidance of how to optimise their diets against targets, using information they provide about current intakes.
Primary Outcome Measures
NameTimeMethod
Usability of myfood246 weeks

System usability scale 1 to 10. HIgher score is better. Online survey.

Secondary Outcome Measures
NameTimeMethod
Correlation between diet and routine measure of body mass index6 weeks

To explore correlations between mean energy intake (kcal/day) as recorded by multiple online 24-hour dietary recalls, with routine BMI in kg/m\^2

Response rate6 weeks

response rates prior to undertaking a full scale randomised controlled trial

Ability of myfood24+ diet optimisation to change diet to meet diet targets6 weeks

myfood24 app allows the healthcare professional to set personalised nutrition targets for the patient. Nutrient intakes will be measured in myfood24 and myfood24+ diet optimisation groups. We will explore differences in nutrient intakes between the groups. Nutrients measured will be daily intake average for energy (kcal), protein (g), fat (g), carbohydrate (g), fibre (g) sodium (g).

Trial Locations

Locations (2)

Gastroenterology surgery

🇬🇧

Leeds, W. Yorks, United Kingdom

Tier 3 Weight Management Clinic

🇬🇧

York, United Kingdom

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