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Personalised Nutrition for Healthy Living (PROTEIN)

Primary Purpose

Diabetes Mellitus, Type 2, PreDiabetes

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Usage of the PROTEIN-Application
Sponsored by
Prof. Dr. med. Andreas F. H. Pfeiffer
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: ≥ 18 years of age Diabetes Type 2 or Prediabetes BMI: 20-kg kg/m2 Android Smart Phone/ Tablet use In good physical health Able to provide written informed consent Exclusion Criteria: Severe endocrine, gastrointestinal, metabolic, cardiovascular, pulmonary, inflammatory or psychiatric disorder Active or recent relevant cancer Currently receiving treatment with Insulin People with disordered eating (such as anorexia nervosa etc.) Those who are not be able to provide written consent

Sites / Locations

  • Charité Univesitätsmedizin Berlin

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Start-Group

Wait-Group

Arm Description

The Start-Group starts with the Protein-Application and wereables for 3 Months and afterwards uses only wereables for 6 Weeks.

The Wait-Group starts with 6 Weeks of using only wereables and afterwards adds the usage of the Protein-Application.

Outcomes

Primary Outcome Measures

Improvement of Time In Range (TIR) by 5%
Our primary objective is to increase the time in range (TIR) of the study participants by 5%
Improve eating behavior towards healthier choices
Improve eating behaviour towards healthier choices during the intervention time

Secondary Outcome Measures

Adherence to dietary recommendations of the app
Adherence to dietary recommendations of the PROTEIN-App
Improvement of glycaemic metabolism
Fasting glucose, HbA1c, HOMA-IR
Reduction in sedentary time
Reduction in sedentary time, defined as: Activity time through fitness trackers or increase in physical activity or increase in steps per day
Aproximation of the energy intake
Approximation of the energy intake (calorie intake and distribution of macronutrients) towards the agreed goals
Measurable change in the faecal microbiome
Measurable change in the faecal microbiome by extraction of DNA and its analysis to identify the relevant species of bacteria
Calculation of the Polygenic Risk Score
Calculation of the Polygenic Risk Score by Isolation of DNA from whole blood

Full Information

First Posted
May 4, 2023
Last Updated
July 24, 2023
Sponsor
Prof. Dr. med. Andreas F. H. Pfeiffer
Collaborators
European Union
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1. Study Identification

Unique Protocol Identification Number
NCT05951140
Brief Title
Personalised Nutrition for Healthy Living
Acronym
PROTEIN
Official Title
Personalised Nutrition for Healthy Living: PROTEIN
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
October 1, 2020 (Actual)
Primary Completion Date
November 30, 2022 (Actual)
Study Completion Date
November 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Prof. Dr. med. Andreas F. H. Pfeiffer
Collaborators
European Union

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The topic of diet and physical activity are of great importance in the treatment of T2D. In the daily routine of a practice or clinic, a doctor has an average of eight minutes per patient, leaving little time for lifestyle issues (Irving et al. 2017). An individualised procedure requires more time and therefore more resources. Currently, an app can be programmed with evidence-based information so that it provides appropriate personalised behavioural recommendations via machine learning. The user gets direct feedback and can make a behavioural change himself. On the one hand, this approach allows better use of doctor-patient time and, on the other hand, the patient learns through positive reinforcement in such a way that his or her behaviour change is supported and reinforced in the longer term and potentially sustainably. The aim of this intervention pilot study within the scope of the EU-Horizon 2020 project is to investigate lifestyle support through a mobile app and wearables to improve lifestyle (personalised nutrition) and important metabolic outcomes in patients with type 2 diabetes or prediabetes. In addition, exploratory genetic and microbiome data will be explored to answer the question of personalisation of the recommendations.
Detailed Description
An inadequate diet and increasing sedentary lifestyle are major contributors to the rise of non-communicable diseases. Individualized recommendations can lead to a healthier lifestyle. The scientific evidence of the effectiveness of health apps offering personalized recommendations is limited. The aim of this intervention pilot study within the scope of the EU-Horizon 2020 project is to investigate lifestyle support through a mobile app and wearables to improve lifestyle (personalised nutrition) and important metabolic outcomes in patients with type 2 diabetes or prediabetes. The Investigators want to asess whether the use of this mobile application that incorporates information of wearables (continuous glucose monitoring and fitness tracker), improves lifestyle and metabolic outcomes in patients with type 2 diabetes (T2D) or prediabetes. Our primary outcome is to improve time in range (TIR) by 5%. It is a prospective randomized control pilot trial with an intervention period of 12 weeks. Participants will use the Protein app, a continuous glucose monitoring system (CGM) and an activity tracker to collect real world data to enable personalisation. In order to identify the effect of the PROTEIN-Application, 300 participants with T2DM or prediabetes will be randomly allocated into two groups: the (1) start-group or the (2) wait-group. The start-group will use an activity tracker, a CGM and the PROTEIN app for 12 weeks followed by a six-week period without the app, but they will use the wearables. The wait-group will use an activity tracker and a CGM, but not the PROTEIN app for six weeks followed by a period of 12 weeks using the PROTEIN app. This study design allowed us to have a control group within the whole cohort and clearly see the influence of the PROTEIN app.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, PreDiabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Start-Group
Arm Type
Experimental
Arm Description
The Start-Group starts with the Protein-Application and wereables for 3 Months and afterwards uses only wereables for 6 Weeks.
Arm Title
Wait-Group
Arm Type
Experimental
Arm Description
The Wait-Group starts with 6 Weeks of using only wereables and afterwards adds the usage of the Protein-Application.
Intervention Type
Other
Intervention Name(s)
Usage of the PROTEIN-Application
Intervention Description
Participants were randomly distributed into 2 groups: (1) Start-Group used the developed Application and wereables to investigate the effect of this support. Participants used the devices and the App for 3 Months followed by a 6-Weeks time of only using wereables and no app, to be able to compare the effects of the Application. (2) The Wait-Group used wereables for 6 Weeks before adding the Protein-App for also 3 Months.
Primary Outcome Measure Information:
Title
Improvement of Time In Range (TIR) by 5%
Description
Our primary objective is to increase the time in range (TIR) of the study participants by 5%
Time Frame
12 Weeks
Title
Improve eating behavior towards healthier choices
Description
Improve eating behaviour towards healthier choices during the intervention time
Time Frame
12 Weeks
Secondary Outcome Measure Information:
Title
Adherence to dietary recommendations of the app
Description
Adherence to dietary recommendations of the PROTEIN-App
Time Frame
12 Weeks
Title
Improvement of glycaemic metabolism
Description
Fasting glucose, HbA1c, HOMA-IR
Time Frame
12 Weeks
Title
Reduction in sedentary time
Description
Reduction in sedentary time, defined as: Activity time through fitness trackers or increase in physical activity or increase in steps per day
Time Frame
12 Weeks
Title
Aproximation of the energy intake
Description
Approximation of the energy intake (calorie intake and distribution of macronutrients) towards the agreed goals
Time Frame
12 Weeks
Title
Measurable change in the faecal microbiome
Description
Measurable change in the faecal microbiome by extraction of DNA and its analysis to identify the relevant species of bacteria
Time Frame
12 Weeks
Title
Calculation of the Polygenic Risk Score
Description
Calculation of the Polygenic Risk Score by Isolation of DNA from whole blood
Time Frame
12 Weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥ 18 years of age Diabetes Type 2 or Prediabetes BMI: 20-kg kg/m2 Android Smart Phone/ Tablet use In good physical health Able to provide written informed consent Exclusion Criteria: Severe endocrine, gastrointestinal, metabolic, cardiovascular, pulmonary, inflammatory or psychiatric disorder Active or recent relevant cancer Currently receiving treatment with Insulin People with disordered eating (such as anorexia nervosa etc.) Those who are not be able to provide written consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lazaros Gymnopoulos, Dr
Organizational Affiliation
Information Technologies Institute, Centre for Research and Technology Hellas
Official's Role
Study Director
Facility Information:
Facility Name
Charité Univesitätsmedizin Berlin
City
Berlin
ZIP/Postal Code
12203
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No

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Personalised Nutrition for Healthy Living

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