- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04758559
Usability of myfood24 in Clinical Populations
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
- usual care
- myfood24Health
- 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.
Studieoversigt
Status
Intervention / Behandling
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Tidlig fase 1
Kontakter og lokationer
Studiekontakt
- Navn: Janet Cade
- Telefonnummer: +447875698368
- E-mail: j.e.cade@leeds.ac.uk
Undersøgelse Kontakt Backup
- Navn: Jean Uniacke
Studiesteder
-
-
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York, Det Forenede Kongerige
- Rekruttering
- Tier 3 Weight Management Clinic
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Kontakt:
- David Locker
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W. Yorks
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Leeds, W. Yorks, Det Forenede Kongerige
- Rekruttering
- Gastroenterology surgery
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Kontakt:
- Cath Moriarty
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-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
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:
-
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Placebo komparator: Usual care
Patients receive usual care concerning dietary advice.
|
Patients will receive standard advice as provided by the clinical team, this may or may not include nutrition.
|
Eksperimentel: myfood24
Patients 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.
|
An app to support monitoring of food and nutrient intake using robust validated methodology.
Andre navne:
|
Eksperimentel: myfood24 + diet optimisation
Personalised 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.
|
An app to support monitoring of food and nutrient intake using robust validated methodology.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Usability of myfood24
Tidsramme: 6 weeks
|
System usability scale 1 to 10. HIgher score is better.
Online survey.
|
6 weeks
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Ability of myfood24+ diet optimisation to change diet to meet diet targets
Tidsramme: 6 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).
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6 weeks
|
Response rate
Tidsramme: 6 weeks
|
response rates prior to undertaking a full scale randomised controlled trial
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6 weeks
|
Correlation between diet and routine measure of body mass index
Tidsramme: 6 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
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6 weeks
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Publikationer og nyttige links
Generelle publikationer
- Wark PA, Hardie LJ, Frost GS, Alwan NA, Carter M, Elliott P, Ford HE, Hancock N, Morris MA, Mulla UZ, Noorwali EA, Petropoulou K, Murphy D, Potter GDM, Riboli E, Greenwood DC, Cade JE. Validity of an online 24-h recall tool (myfood24) for dietary assessment in population studies: comparison with biomarkers and standard interviews. BMC Med. 2018 Aug 9;16(1):136. doi: 10.1186/s12916-018-1113-8.
- Carter MC, Albar SA, Morris MA, Mulla UZ, Hancock N, Evans CE, Alwan NA, Greenwood DC, Hardie LJ, Frost GS, Wark PA, Cade JE; myfood24 Consortium. Development of a UK Online 24-h Dietary Assessment Tool: myfood24. Nutrients. 2015 May 27;7(6):4016-32. doi: 10.3390/nu7064016.
Hjælpsomme links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- IRAS 266347
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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