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STOP DIABETES - Knowledge-based Solutions (StopDia)

Primary Purpose

Type2 Diabetes, Life Style, Diet Habit

Status
Recruiting
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
Digital lifestyle intervention group
Combined digital and face-to-face lifestyle intervention group
Sponsored by
University of Eastern Finland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Type2 Diabetes focused on measuring Prevention, Digital solutions, Type 2 diabetes, Life style modification, Physical activity, Healthy diet, Health economics, Environmental choice architecture, Socio-economic facilitators, Socio-economic barriers, Wellbeing

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • age of 18-70 years
  • 12 points or more in the Finnish diabetes risk score or previous gestational diabetes or repeated impaired fasting glucose (IFG) (fasting plasma glucose level 6,1 - 6,9 mmol/l) or impaired glucose tolerance (2-hour glucose level 7,8 - 11,0 mmol/l in oral glucose tolerance test)
  • living in the hospital district of Northern Savo, PΓ€ijΓ€t-HΓ€me or South Karelia
  • possibility to use computer, smartphone or tablet with internet connection
  • having own self-phone number
  • adequate Finnish language skill

Exclusion Criteria:

  • type 1 or 2 diabetes
  • pregnancy or breastfeeding
  • current cancer or less than 6 months from the end of cancer treatment

Sites / Locations

  • University of Eastern FinlandRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Control group

Digital lifestyle intervention group

Combined digital and face-to-face lifestyle intervention group

Arm Description

At baseline, individuals in the control group receive digital information package about lifestyle risk factors of type 2 diabetes with recommendations on healthy diet and physical activity in accordance with the Finnish Nutrition Recommendations and the national recommendation for health enhancing physical activity.

Participants are instructed to use a digital self-help tool for 12 months. This tool is developed in the StopDia-study to enact positive changes in participant's health behaviour. The digital intervention consists of 2 components which motivate, enable and trigger the participants to improve their health behaviours. B.J. Fogg's Tiny Habits -ideology. The digital intervention is based on the Fogg Behaviour Model (FBM) and the Behaviour Wizard.

Participants are using the StopDia digital solution tool as described above. In addition, they have six face-to-face group coaching (6-15 participants/group) sessions at local health centers facilitated by trained nurses. The face-to-face group intervention is based on the Self-Determination Theory and theories of self-regulation, and delivered using intrinsic motivational coaching approach designed and tested in the GOAL lifestyle intervention, and further developed in several other studies in Finland and internationally.

Outcomes

Primary Outcome Measures

Change in diet
Change in diet is assessed by the dietary score based on Finnish Nutrition Recommendations and is formulated according to food frequency questionnaire.
Change in total physical activity level
Change in total physical activity level is assessed by the physical activity questionnaire.
Change in plasma glucose levels
Assessed in the 2 hour oral glucose tolerance tests
Change in body weight
Assessed with digital weight scales

Secondary Outcome Measures

Change in waist circumference
Assessed with validated guidelines for the measure
Change in insulin concentration
Assessed in the 2 hour oral glucose tolerance tests
Change in glycated hemoglobin
Assessed from fasting blood sample
Change in plasma lipid concentration
Plasma total, HDL and LDL cholesterol, and triglyceride concentrations are measured.
Change in resting blood pressure
Resting systolic and diastolic blood pressure is measured by automatic sphygmomanometer in sitting position.
Change in inflammation markers
Serum high-sensitivity C-reactive protein (hs-CRP) and interleukine-1Ra (IL-1Ra) are measured as biomarkers of inflammation.
Change in liver function
Plasma aspartate aminotransferase (AST) and alanine aminotransferase (ALT) are measured as biomarkers of liver function.
Change in metabolite profiles
Metabolites and metabolic profiles related to diet, other lifestyle factors and predicting type 2 diabetes measured from serum and plasma samples
Change in sedentary behavior
Change in sedentary behavior is described as the total amount spent in sitting and lying position during waking hours, and is assessed by the questionnaire.
Change in sleeping behavior
Formulated according to sleeping behavior questionnaire
Change in smoking behavior
Assessed by questionnaire
Change in alcohol consumption
Assessed by food frequency questionnaire
Change in eating behavior
Eating behavior is assessed by questionnaires.
Change in mental wellbeing
Change in mental wellbeing is assessed by questionnaire.
Change in quality of life
Quality of life is assessed by questionnaire.
Use of health-care services and associated costs
Use of health-care services are assessed by questionnaire and registers. Associated costs are calculated based on these data.
Work ability and associated costs
Work ability is assessed by questionnaire. Associated costs are calculated based on these data.
User experience of the Internet intervention
Measured by the questionnaires.
Usage of the Internet intervention
Measured by the log data

Full Information

First Posted
April 13, 2017
Last Updated
May 15, 2017
Sponsor
University of Eastern Finland
Collaborators
National Institute of Health and Welfare, Technical Research Centre of Finland, University of Melbourne, University of Konstanz, Karolinska Institutet, Maastricht University, University of Oslo, Danube-University, Flinders University, Cornell University, University of Copenhagen, Roskilde University, University of Manchester, University of York
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1. Study Identification

Unique Protocol Identification Number
NCT03156478
Brief Title
STOP DIABETES - Knowledge-based Solutions
Acronym
StopDia
Official Title
STOP DIABETES - Knowledge-based Solutions
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Recruiting
Study Start Date
April 10, 2017 (Actual)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2037 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Eastern Finland
Collaborators
National Institute of Health and Welfare, Technical Research Centre of Finland, University of Melbourne, University of Konstanz, Karolinska Institutet, Maastricht University, University of Oslo, Danube-University, Flinders University, Cornell University, University of Copenhagen, Roskilde University, University of Manchester, University of York

4. Oversight

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

5. Study Description

Brief Summary
The aim of the Stop Diabetes - Knowledge based solutions (StopDia) consortium project (University of Eastern Finland, National Institute for Health and Welfare, and Technical Research Centre of Finland) is to develop and test approaches to identify individuals at increased risk of type 2 diabetes and to empower them in adopting and maintaining a healthy lifestyle by combining individual and environment level strategies into a dual-process approach targeting deliberative and automatic processes of behavior. We also aim to identify barriers and facilitators of adopting a healthy lifestyle in the society, create a model for the prevention of type 2 diabetes by joint actions of health care, third sector, and other societal actors, and develop methods to monitor the cost-effectiveness of these actions. We will carry out a 1-year randomized controlled trial on the effects of among 10 000 individuals aged 18-70 years at increased risk of type 2 diabetes living in Finland. The participants will be randomized into the control group, the digital lifestyle intervention group, or the combined digital and face-to-face lifestyle intervention group. The aim of the interventions is to enhance diet quality, increase physical activity, decrease body weight, and improve glucose tolerance in individuals at increased risk of type 2 diabetes.
Detailed Description
Type 2 diabetes is a major public health and economical problem all over the world, including Finland. A healthy diet and physical activity are the cornerstones for the prevention of type 2 diabetes. The aim of the Stop Diabetes - Knowledge based solutions (StopDia) study is to develop and test approaches to identify individuals at increased risk of type 2 diabetes and to empower them in adopting and maintaining a healthy lifestyle by combining individual and environment level strategies into a dual-process approach targeting deliberative and automatic processes of behavior. We also aim to identify barriers and facilitators of adopting a healthy lifestyle in the society, create a model for the prevention of type 2 diabetes by joint actions of health care, third sector, and other societal actors, and develop methods to monitor the cost-effectiveness of these actions. We will recruit 10 000 individuals aged 18-70 years at increased risk of type 2 diabetes living in the hospital district of Northern Savo, PΓ€ijΓ€t-HΓ€me, or South Karelia in Finland for a 1-year randomized controlled trial. We will assess body height and weight, body mass index, waist circumference, and blood pressure, take blood samples for biochemical analyses, and perform a 2-hour oral glucose tolerance test at baseline. The participants will be asked to fill out a detailed digital questionnaire on factors related to the risk of type 2 diabetes, including diet, physical activity, sedentary behavior, health status, physical, psychic, and social well-being, as well as the use of health care services and medications. The participants will be randomized into the control group, the digital lifestyle intervention group, or the combined digital and face-to-face lifestyle intervention group. The aim of the interventions is to enhance diet quality, increase physical activity, decrease body weight, and improve glucose tolerance in individuals at increased risk of type 2 diabetes. We will also investigate the effects of environmental interventions at certain workplaces and the synergistic effects of the individual level and environmental interventions in a subsample of the study population. All baseline assessments will be repeated after the 1-year follow-up. The primary outcomes will be the changes in diet, total physical activity, body weight, and plasma glucose levels from the oral glucose tolerance test. After the 1-year intervention study, follow-up examinations will be performed 3, 5, 10, 15, and 20 years after the baseline examinations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type2 Diabetes, Life Style, Diet Habit, Physical Activity, Empowerment
Keywords
Prevention, Digital solutions, Type 2 diabetes, Life style modification, Physical activity, Healthy diet, Health economics, Environmental choice architecture, Socio-economic facilitators, Socio-economic barriers, Wellbeing

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomized in 3 groups: 1) control group, 2) digital lifestyle intervention group and 3) combined digital and face-to-face lifestyle intervention group. Environmental changes will be done within some work places.Part of the participants in each group may be exposed to environmental modification that are aimed for lifestyle changes at work places.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
10000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
No Intervention
Arm Description
At baseline, individuals in the control group receive digital information package about lifestyle risk factors of type 2 diabetes with recommendations on healthy diet and physical activity in accordance with the Finnish Nutrition Recommendations and the national recommendation for health enhancing physical activity.
Arm Title
Digital lifestyle intervention group
Arm Type
Experimental
Arm Description
Participants are instructed to use a digital self-help tool for 12 months. This tool is developed in the StopDia-study to enact positive changes in participant's health behaviour. The digital intervention consists of 2 components which motivate, enable and trigger the participants to improve their health behaviours. B.J. Fogg's Tiny Habits -ideology. The digital intervention is based on the Fogg Behaviour Model (FBM) and the Behaviour Wizard.
Arm Title
Combined digital and face-to-face lifestyle intervention group
Arm Type
Experimental
Arm Description
Participants are using the StopDia digital solution tool as described above. In addition, they have six face-to-face group coaching (6-15 participants/group) sessions at local health centers facilitated by trained nurses. The face-to-face group intervention is based on the Self-Determination Theory and theories of self-regulation, and delivered using intrinsic motivational coaching approach designed and tested in the GOAL lifestyle intervention, and further developed in several other studies in Finland and internationally.
Intervention Type
Behavioral
Intervention Name(s)
Digital lifestyle intervention group
Intervention Description
Intervention with digital application for lifestyle changes
Intervention Type
Behavioral
Intervention Name(s)
Combined digital and face-to-face lifestyle intervention group
Intervention Description
Intervention with digital application and group meetings for lifestyle changes
Primary Outcome Measure Information:
Title
Change in diet
Description
Change in diet is assessed by the dietary score based on Finnish Nutrition Recommendations and is formulated according to food frequency questionnaire.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in total physical activity level
Description
Change in total physical activity level is assessed by the physical activity questionnaire.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in plasma glucose levels
Description
Assessed in the 2 hour oral glucose tolerance tests
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in body weight
Description
Assessed with digital weight scales
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Secondary Outcome Measure Information:
Title
Change in waist circumference
Description
Assessed with validated guidelines for the measure
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in insulin concentration
Description
Assessed in the 2 hour oral glucose tolerance tests
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in glycated hemoglobin
Description
Assessed from fasting blood sample
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in plasma lipid concentration
Description
Plasma total, HDL and LDL cholesterol, and triglyceride concentrations are measured.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in resting blood pressure
Description
Resting systolic and diastolic blood pressure is measured by automatic sphygmomanometer in sitting position.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up.
Title
Change in inflammation markers
Description
Serum high-sensitivity C-reactive protein (hs-CRP) and interleukine-1Ra (IL-1Ra) are measured as biomarkers of inflammation.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up.
Title
Change in liver function
Description
Plasma aspartate aminotransferase (AST) and alanine aminotransferase (ALT) are measured as biomarkers of liver function.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up.
Title
Change in metabolite profiles
Description
Metabolites and metabolic profiles related to diet, other lifestyle factors and predicting type 2 diabetes measured from serum and plasma samples
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in sedentary behavior
Description
Change in sedentary behavior is described as the total amount spent in sitting and lying position during waking hours, and is assessed by the questionnaire.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in sleeping behavior
Description
Formulated according to sleeping behavior questionnaire
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in smoking behavior
Description
Assessed by questionnaire
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in alcohol consumption
Description
Assessed by food frequency questionnaire
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in eating behavior
Description
Eating behavior is assessed by questionnaires.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in mental wellbeing
Description
Change in mental wellbeing is assessed by questionnaire.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Change in quality of life
Description
Quality of life is assessed by questionnaire.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up.
Title
Use of health-care services and associated costs
Description
Use of health-care services are assessed by questionnaire and registers. Associated costs are calculated based on these data.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up
Title
Work ability and associated costs
Description
Work ability is assessed by questionnaire. Associated costs are calculated based on these data.
Time Frame
From baseline to one year follow-up, to 3 year follow-up, to 5 year follow-up, to 10 year follow-up, to 15 year follow-up, 20 year follow-up.
Title
User experience of the Internet intervention
Description
Measured by the questionnaires.
Time Frame
During the intervention at the time point of two weeks, and at one year follow-up
Title
Usage of the Internet intervention
Description
Measured by the log data
Time Frame
During the intervention at the time point of two weeks, 3 months, 6 months, and at one year follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: age of 18-70 years 12 points or more in the Finnish diabetes risk score or previous gestational diabetes or repeated impaired fasting glucose (IFG) (fasting plasma glucose level 6,1 - 6,9 mmol/l) or impaired glucose tolerance (2-hour glucose level 7,8 - 11,0 mmol/l in oral glucose tolerance test) living in the hospital district of Northern Savo, PΓ€ijΓ€t-HΓ€me or South Karelia possibility to use computer, smartphone or tablet with internet connection having own self-phone number adequate Finnish language skill Exclusion Criteria: type 1 or 2 diabetes pregnancy or breastfeeding current cancer or less than 6 months from the end of cancer treatment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jussi PihlajamΓ€ki, MD, PhD
Phone
+358 50 344 0187
Email
jussi.pihlajamaki@uef.fi
First Name & Middle Initial & Last Name or Official Title & Degree
Timo A Lakka, MD, PhD
Phone
+358 40 7707 329
Email
timo.lakka@uef.fi
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jussi PihlajamΓ€ki, MD, PhD
Organizational Affiliation
University of Eastern Finland
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Eastern Finland
City
Kuopio
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jussi PihlajamΓ€ki, MD, PhD
Phone
+358 50 344 0187
Email
jussi.pihlajamaki@uef.fi

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35200147
Citation
Lavikainen P, Mattila E, Absetz P, Harjumaa M, Lindstrom J, Jarvela-Reijonen E, Aittola K, Mannikko R, Tilles-Tirkkonen T, Lintu N, Lakka T, van Gils M, Pihlajamaki J, Martikainen J. Digitally Supported Lifestyle Intervention to Prevent Type 2 Diabetes Through Healthy Habits: Secondary Analysis of Long-Term User Engagement Trajectories in a Randomized Controlled Trial. J Med Internet Res. 2022 Feb 24;24(2):e31530. doi: 10.2196/31530.
Results Reference
derived
PubMed Identifier
33302264
Citation
Karlund A, Kaariainen T, Kostamo VM, Kokkola T, Kolehmainen M, Lakka TA, Pihlajamaki J, Manninen A. Oxygen-18 and carbon-13 isotopes in eCO2and erythrocytes carbonic anhydrase activity of Finnish prediabetic population. J Breath Res. 2021 Jan 22;15(2). doi: 10.1088/1752-7163/abd28d.
Results Reference
derived
PubMed Identifier
32779571
Citation
Harjumaa M, Absetz P, Ermes M, Mattila E, Mannikko R, Tilles-Tirkkonen T, Lintu N, Schwab U, Umer A, Leppanen J, Pihlajamaki J. Internet-Based Lifestyle Intervention to Prevent Type 2 Diabetes Through Healthy Habits: Design and 6-Month Usage Results of Randomized Controlled Trial. JMIR Diabetes. 2020 Aug 11;5(3):e15219. doi: 10.2196/15219.
Results Reference
derived
PubMed Identifier
30823909
Citation
Pihlajamaki J, Mannikko R, Tilles-Tirkkonen T, Karhunen L, Kolehmainen M, Schwab U, Lintu N, Paananen J, Jarvenpaa R, Harjumaa M, Martikainen J, Kohl J, Poutanen K, Ermes M, Absetz P, Lindstrom J, Lakka TA; StopDia study group. Digitally supported program for type 2 diabetes risk identification and risk reduction in real-world setting: protocol for the StopDia model and randomized controlled trial. BMC Public Health. 2019 Mar 1;19(1):255. doi: 10.1186/s12889-019-6574-y.
Results Reference
derived
Links:
URL
http://www.stopdia.fi/briefly-in-english
Description
short description in English

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STOP DIABETES - Knowledge-based Solutions

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