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OverweightPROTEINNCT04829851

The PROTEIN Project

An observational study of Overweight and Nutritional Deficiency, run by University of Surrey at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

New advances in information computer technology and artificial intelligence (AI) offer the possibility to create a personalized tool and support system for healthy living and eating, and this is the principal objective of the PROTEIN Project (an EU-funded consortium; Horizon 2020). Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Overweight, Nutritional Deficiency, Poor Nutrition
What is being tested?
PROTEIN Mobile App and Expert Dashboard
How many people
120 participants
Where
1 siteUnited Kingdom
Study dates
1 Oct 2021to 30 Dec 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: General public within the local area (Surrey, UK)

Who may be able to join

  • Overweight group:
  • ≥ 18 years of age
  • BMI: 25 - 30 kg/m2
  • In good physical health
  • Not a regular user of another nutrition support application (such as MyFitnessPal)
  • Able to provide written informed consent
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  • Android Smart Phone/ Tablet user
  • Individuals with poor quality diet
  • deficiencies:
  • ≥ 18 years of age
  • Diagnosed iron deficiency
  • In good physical health
  • Not a regular user of another nutrition support application (such as MyFitnessPal)
  • Able to provide written informed consent
  • Android Smart Phone/ Tablet user Individuals with poor quality diet
  • low fruit and vegetable intake:
  • ≥ 18 years of age
  • Low fruit and vegetable intakes (< 2-3 portions/ day)
  • In good physical health
  • Not a regular user of another nutrition support application (such as MyFitnessPal)
  • Able to provide written informed consent
  • Android Smart Phone/ Tablet user
  • Health care professionals
  • Registered health care professional; General Practitioner/ Dietitian/ Nutritionist/ Registered Exercise Professionals (REPs) etc who sees clients for assistance with weight management and/ or iron deficiency or diet quality.
  • Willing to trial a new nutrition support application with their patients
  • Android Smart Phone/ Tablet user

Who cannot join

  • Overweight group:
  • Those who have been diagnosed with cardiovascular disease, type 1 diabetes mellitus or type 2 diabetes mellitus.
  • Currently receiving treatment for long term medical conditions
  • Clinically significant haematological abnormalities or an active malignancy
  • Regular exercisers (more than 150 minutes of moderate exercise per week or > 75 minutes of high intensity exercise)
  • People who are unable to exercise for medical reasons or for whom exercise is otherwise contra-indicated by a health professional
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  • People with disordered eating (such as anorexia nervosa etc.)
  • Those who are not be able to provide written consent.
  • Those who are unable to read/write sufficiently to provide consent and complete study materials
  • Individuals with deficiencies and poor-quality diet:
  • Those who have been diagnosed with cardiovascular disease, type 1 diabetes mellitus or type 2 diabetes mellitus.
  • Currently receiving treatment for long term medical conditions.
  • Clinically significant haematological abnormalities or an active malignancy
  • Regular exercisers (more than 150 minutes of moderate exercise per week or > 75 minutes of high intensity exercise)
  • People who are unable to exercise for medical reasons or for whom exercise is otherwise contra-indicated by a health professional
  • People with disordered eating (such as anorexia nervosa etc.)
  • Those who are not be able to provide written consent.
  • Those who are unable to read/write sufficiently to provide consent and complete study materials
  • Health Care Professionals:
  • Not affiliated/ registered health care professional
  • Do not have any clients/ patients that fall into one of the groups above (overweight, iron deficiency or low fruit/ vegetable consumption).

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • University of Surrey

    Guildford, GU27XH

Other trials in United Kingdom

About this study

Official title: Personalised Nutrition for Healthy Living: The PROTEIN Project

New advances in information computer technology and artificial intelligence (AI) offer the possibility to create a personalized tool and support system for healthy living and eating, and this is the principal objective of the PROTEIN Project (an EU-funded consortium; Horizon 2020). In order to obtain information on the acceptability, usability and its effectiveness at facilitating behaviour change of the application within the home and store. A pilot trial will be conducted in participants who are overweight (BMI 25-29.9 kg/m2) and a separate group of participants who consume a low quality diet (low in fruit and vegetable intake) and/or have a nutrition deficiency (specifically iron-deficiency anaemia).

During this study the subjects will be asked to attend the lab (or remotely due to covid restrictions) at the beginning of the study for baseline measurements and instructions on how to use / download the mobile application. Participants will have their anthropometrics measured (including height/ weight/ waist: hip circumference). The PROTEIN application will collect self-reported data from the user, which includes: user profile input, dietary and fluid intake, daily physical activity (such as step count), biochemistry, sleep and chewing (in- meal behaviour). Information on how users will interact with the app, which screens they use, how many log ons and how often data is inputted will also be collected. Throughout the trial, the participants will be contacted via the application or by the researchers to request feedback on their progress and to encourage reporting of any issues.

Health care professionals will also be recruited to test the expert dashboard of the PROTEIN app. Through this system they will be able to provide nutrition/ physical activity advice directly to their patients and input their relevant biochemical results (such as haemoglobin for anaemic patients).

Read the detailed description

During this study the subjects will be asked to visit the lab followed between 4 and 16 weeks usage of the PROTEIN app and then a final lab visit.

In the event that COVID-19 restrictions continue and prevent, or restrict, face-to-face visits a completely remote study protocol will also be developed and used in place of the study below.

  1. Advertising and Recruitment:
  2. General public: Prospective users will be recruited by the University of Surrey via social media (e.g. Facebook and Twitter), posters and flyers in the local area and emails sent to University staff and students. With the permission on the relevant group leaders,' overweight participants will be recruited via local commercial weight loss groups. With the permission of the practice managers recruitment via GP practices will also be undertaken, with practice registers screened by a member of practice staff and information/ invitation letters sent to those who meet the inclusion criteria (no details will be shared with the research team). Flyers will also be distributed to local relevant outpatient clinics, e.g. haematology and dietetic with the permission of the clinic managers. Participants will also be recruited through health care professionals (HCP) in the local area following identification of suitable HCPs (see below) ii) Health Care Professionals (HCPs): HCPs involved in supporting the dietary or activity goals of target clients will also be recruited to the HCP arm of the study. The project will be promoted through local (and, if remote, National) professional networks and professional body membership lists, newsletters and via relevant social media channels. HCPs will have the option to participate in a desk-based expert review of the application (without registering specific clients) with respect to its usability or to register one or more of their own clients on the app via the user dashboard to participate in the efficacy review. In the latter case suitable clients identified by the HCP will be required to also register with the trial. The HCP will be provided with flyers and invitation letters to allow them to make first contact with the client who will be asked to contact the research team to confirm their willingness to participate, ensuring no personal data is shared prior to consent being received.
  3. Baseline measurements:
  4. Public, Face to face: Users will attend the lab and will then have their body composition measured (to include their height, weight, waist and hip circumference) by the researchers. ii) Public, Remote: An alternative remote protocol will utilise Zoom/ Microsoft teams video call. These will be arranged by the researchers with the participants to take them through self-completion of the baseline measures and procedures. iii) HCPs: HCPs will be contacted via email and will also be invited to either attend the lab or meet with the researchers utilizing Zoom/ Microsoft teams to discuss the usage of the expert dashboard.
  5. PROTEIN app usage for public: Following this, the users will be requested to log the following details to set-up the PROTEIN system: contact details (name/ email/phone number), age, gender, height, weight, ethnicity, morbidity status (such as cardiovascular disease/ diabetes mellitus etc.), education/ socioeconomic status, smoking status, diet or drink habits (such as vegetarian/ vegan/ dairy-free etc.), and medication. Daily food and fluid intake will be collected via the PROTEIN app and will be self-reported by the user/ participant. Users will be asked to log all dietary and fluid intake for 7 days per week (to include the weekend) into the home PROTEIN application suite. Users will either use their respective smartwatches/activity trackers or manually input the relevant data into the home PROTEIN application suite. In the former case, physical activity and sleep data will be collected in daily summaries as provided by Google Fit (or a suitable alternative, such as Garmin, FitBit, Polar, Apple watch etc.). Smart watches may be provided free of charge for a subset of users (subject to trial resources) and there may also be an opportunity for participants to use their own existing smartwatches. In the latter case, users will be requested to manually log daily activity data, for 7 days per week. Users will be monitored by the PROTEIN artificial intelligence (AI) system for deviations from their suggested plan and for any meal or activity swaps requested to check for adherence/ compliance to the recommendations suggested by the PROTEIN AI system. A subset of users who are also registered with OCADO will receive food shopping recommendations (in the form of a shopping list) tailored to their nutritional requirements and targets; budget will also be taken into account. Participants will be asked to indicate all food products that they swapped/ bought and for whom they bought them within the PROTEIN application suite. This will be conducted in partnership with OCADO.
  6. After at least 4 weeks of usage, data will be collected regarding the user and HCP experience via an online questionnaire through the PROTEIN app or sent usability questionnaires via email by the researchers.
  7. Follow-up measures:
  8. Public, Face to face: Users will attend the lab after at least 4 weeks of usage and will then have their body composition remeasured (to include their height, weight, waist and hip circumference) by the researchers. They will also be asked to provide feedback on the usability of the application by completing two questionnaires on the 1) usability of the application and 2) suitability for general public use. ii) Public, Remote: An alternative remote protocol will utilise Zoom/ Microsoft teams video call. These will be arranged by the researchers with the participants to take them through self-completion of the follow-up measures following at least 4 weeks of usage. Participants will be asked to provide feedback via two online questionnaires on the 1) usability of the application and 2) suitability for general public use. iii) HCPs: HCPs will be contacted via email and will also be invited to either attend the lab or meet with the researchers utilizing Zoom/ Microsoft teams to discuss their feedback following usage of the expert dashboard for at least 4 weeks. They will be asked to provide feedback via two questionnaires on the 1) usability of the application and 2) suitability for usage by health care professionals. A subset of participants (from all groups), representing both those who have engaged or not with the app, will also be contacted by the researchers after their trial period has ended and invited to take part in additional qualitative measures, such as focus group interviews to provide more feedback on their experience of the PROTEIN app.
Being tested
PROTEIN Mobile App, Expert Dashboard
Medical subject headings
Overweight, Malnutrition, Anemia, Iron-Deficiency

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PROTEIN Mobile AppDevice

    All recruited user groups will be expected to use the PROTEIN app. During this study the subjects will be asked to visit the lab followed by at least 4 weeks usage of the PROTEIN app and then a final lab visit.

  • Expert DashboardDevice

    Health care professionals (HCP) will be contacted via email and will also be invited to either attend the lab or meet with the researchers utilizing Zoom/ Microsoft teams to discuss the usage of the expert dashboard within the PROTEIN application.

Study groups in NCT04829851
Study groupRoleWhat they receive
Health Care ProfessionalsRegistered health care professional, such as a General Practitioner/ Dietitian/ Nutritionist/ Registered Exercise Professional (REPs) etc. who sees clients for assistance with weight management and / or iron deficiency or diet quality.
Receives: Device: Expert Dashboard
Adults who are OverweightAdults (> 18 years) who are considered to be overweight (25 - 30 kg/m2) but are otherwise in good physical health and a regular android smart phone/ tablet user.
Receives: Device: PROTEIN Mobile App
Adults with Iron Deficiency AnaemiaAdults (> 18 years) who have been diagnosed with Iron deficiency anaemia but are otherwise in good physical health and a regular android smart phone/ tablet user.
Receives: Device: PROTEIN Mobile App
Adults with Low- Fruit/ Vegetable IntakeAdults ( > 18 years) with a low fruit and vegetable intake (2-3 portions/ d) but are otherwise in good physical health and a regular android smart phone/ tablet user.
Receives: Device: PROTEIN Mobile App

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Feasibility of the PROTEIN mobile application's ability to facilitate a lifestyle change

    Users will be requested to set up the application on their smartphone / tablet, following this the users will be provided with a suggested plan through the artificial intelligence (AI) system. Users will be asked to log all dietary and fluid intake for 7 days per week into the PROTEIN application suite. Therefore, the primary outcome measure will be the adherence/ compliance to the recommendations suggested by the PROTEIN AI system following up to 4 weeks of usage of the mobile application.

    Measured: At least 4 weeks

Secondary outcomes (4)
  1. Shopping acceptability within the application

    A subset of users who are also registered with OCADO will receive food shopping recommendations (in the form of a shopping list) tailored to their nutritional requirements and targets: budget will also be taken into account. Users will be asked to indicate the acceptability of this function within the mobile application after at least 4 weeks of usage.

    Measured: At least 4 weeks

  2. Efficacy of the PROTEIN application to monitor within-meal chewing

    Within-meal behaviours will be analysed through the application on at least 4 separate occasions during their 4-week usage of the application. The users will be asked to record themselves eating a meal within the PROTEIN application, which will calculate their chew count. Therefore, the efficacy of the system will be ealuated for within-meal chewing behaviours by all users.

    Measured: At least 4 weeks

  3. User Satisfaction with the PROTEIN Application

    A subset of participants (from all groups), representing both those who have engaged or not with the app, will be contacted by the researchers after their trial period has ended and invited to take part in additional qualitative measures, such as focus group interviews to provide more user satisfaction feedback on their experience of the PROTEIN application.

    Measured: At least 4 weeks

  4. Suitability and usability review of the PROTEIN application for Health Care Professionals

    Health care professionals (HCP) will be involved in supporting the dietary or activity goals of target clients recruited. HCPs will have the option to participate in a desk-based expert review of the application (without registering specific clients) with respect to its usability or to register one or more of their own clients on the app via the user dashboard to participate in the efficacy review. They will be asked to provide feedback via two questionnaires on the 1) usability of the application and 2) suitability for usage by health care professionals.

    Measured: At least 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Apr 2021
  2. Study start1 Oct 2021
  3. Primary completion4 Nov 2022
  4. Study completion30 Dec 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
120 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04829851
Sponsor's protocol ID
PROTEIN
Acronym
PROTEIN
Status last verified
May 2023
First submitted
25 Mar 2021
Last updated
16 May 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Overweight and Nutritional Deficiency, run by University of Surrey at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 26 inclusion and 21 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 May 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Feasibility of the PROTEIN mobile application's ability to facilitate a lifestyle change (time frame: At least 4 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 May 2023.

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The PROTEIN Project (NCT04829851) | AzTrials