Assessment of the Health and Lifestyle Tool

Study to Evaluate the Digital Health and Lifestyle Tool Developed at the University of Gothenburg

The overall aim of the study is to evaluate a digital lifestyle intervention that has been developed in an academic setting at the University of Gothenburg, Sweden. The tool is based on self-affirmation theory and has large emphasis on self-reflection to enable sustainable lifestyle changes. The effects of the tool on HbA1c, reflecting long-term blood glucose, will be evaluated in patients with type 2 diabetes. The study will contain two phases. The study consists of a three-month period in which participants are randomly assigned to usual care or access to the intervention tool, followed by an open-label three-year observation period during which participants have access to the tool in addition to ordinary healthcare and are compared with matched controls on usual care.

Study Overview

• Status: Active, not recruiting
• Conditions: Diabetes Mellitus, Type 2
• Intervention / Treatment: Behavioral: Health and lifestyle tool; Other: Usual care

Detailed Description

Considerable evidence suggest that lifestyle interventions can prevent or delay the onset of type 2 diabetes, and self-care behaviors largely determine HbA1c. Modifiable lifestyle factors have been established as key drivers of disease onset, progression, and prognosis, motivating the use of "lifestyle as medicine". Despite this, a substantial number of patients with type 2 diabetes (T2D) have difficulties attaining adequate glycemic control.

Lifestyle interventions are often complex and difficult to implement on a large scale. Digital health interventions are increasingly incorporated into diabetes care, and have the potential to improve both behavioral and clinical outcomes on a broad basis. However, low levels of uptake, reduced user engagement over time, and low acceptance among patients, raise concerns about their effectiveness. Knowledge on how to design interventions aimed at inducing change by promoting motivation and personal engagement, as well as a better understanding of patient interaction with digital health interventions, could help overcome these challenges and inform the development of a novel and effective health support.

The objective or this study is to evaluate a new web-based tool, developed at the University Gothenburg, Sweden, that aims to support patient autonomy and motivation to make sustainable lifestyle changes.

The investigators will test the hypothesis that users of the tool get improved HbA1c relative to baseline as compared with controls on usual care.

Overall study design The study is an investigator-initiated single-center study conducted at Skåne University Hospital, Sweden, and will follow participants over three years.

Participants with T2D will be recruited by sending letters with study information to patients in the ANDIS (All New Diabetics In Scania) registry in Sweden or by advertisements. If HbA1c is 52 mmol/mol or above participants are included and attend study visits every three months during the first year and every sixth month during the following two years for blood sampling and physical examination.

The study has an initial 3-month randomization period. Thereafter, all participants get access to the tool and used it during an open-label observation period of up to three years.

Study procedures All participants receive an email with a link to their personal account on the tool. This email is sent immediately after the initial visit. Via the link participants set a password, complete an initial questionnaire and are then randomized to immediate access the tool or to be on a three-month wait list (1:1 ratio).

The randomization is performed by a web-based system, using a block size of eight. Randomization is unknown to all participants when completing the initial questionnaire and is also unknown to the study personnel at the initial study visit. Thereafter, randomization is non-blinded, i.e. there is full transparency as to who get access to the tool and not.

Those randomized to the wait list receive usual care, which means that participants are followed by their ordinary healthcare provider. Those participants do not receive any information about the tool or its content during the three-month period. Participants who are randomized to wait receive an invitation to a second study visit after three months. Following the visit, an email is sent with a link to complete the questionnaire after which the tool can be accessed.

Study visits Every physical study visit lasts appr. 20 minutes and includes measurements of length and weight, blood pressure, and estimations of fat and muscle mass by bioimpedance. Fasting blood samples are taken for analysis of HbA1c and other cardiometabolic proteins. Participants will not receive any counselling or lifestyle advice at the study visits. Technical problems are referred to the study coordinator, who may also respond to requests to clarify content in a general manner without providing personal advice. Patients are followed by their ordinary physician throughout the study, i.e. the tool is provided on top of ordinary anti-diabetic treatment and healthcare contacts.

The intervention The tool is web-based and used via a computer or mobile phone. It is used at each individual's preferred pace but participants are recommended to login at least every other week. Every round the participants choose a themes (out of appr. 80 possible covering e.g. food, exercise, stress, self-reflection aspects), which takes appr. 15-30 minutes to complete. Participants then reflect on the content and how it could be implemented in daily life. When returning for next round participants are asked to reflect on any changes done since last time. There is no interaction between individual participants.

Statistics As one primary endpoint an intention-to-treat analysis is used to compare HbA1c between the two randomization groups based on data between first and second visit (DeltaHbA1c). Patients lost to follow-up between first and second visit will not be included in the analysis.

The standard deviation of DeltaHbA1c is 6 mmol/mol over 3 months in ANDIS patients with baseline HbA1c at 52 mmol/mol or above. With 80% power at alpha=0.05, 142 participants are needed to each randomization arm to detect a significant difference between the groups, assuming that the true treatment effect of the intervention is 2 mmol/mol over 3 months.

Enrollment will continue until the required number of participants are reached, accounting for those lost to follow-up during the randomization period.

As another primary endpoint, investigators will during the open-label observation period compare DeltaHbA1c at one year relative to baseline between patients using the tool as recommended and matched controls with usual care(1:2 ratio between exposed and controls).

The standard deviation of DeltaHbA1c is 7 mmol/mol over one year (as observed in patients with baseline HbA1c at 52 mmol/mol or above in the ANDIS cohort). With 80% power at alpha=0.05, 24 participants using the tool as recommended and 48 matched controls are needed to detect a significant difference between the groups, assuming that the true treatment effect of the intervention is 5 mmol/mol.

Subanalysis of MOD patients A data-driven cluster analysis of 9,000 diabetes patients has been performed in the ANDIS registry based on six variables measured at diagnosis: GAD antibodies, age, BMI, HbA1c (reflecting long-term blood glucose), HOMA2-B (reflecting insulin secretion) and HOMA2-IR (reflecting insulin resistance). Four clusters of T2D patients were highlighted, each with different characteristics and risk of complications. One of these cluster, MOD (Mild Obesity-related Diabetes), is characterized by high BMI and insulin resistance but relatively well-preserved insulin secretion. It has been suggested that patients with MOD characteristics would benefit particularly from lifestyle changes. The investigators therefore hypothesize that patients with MOD characteristics would benefit particularly well from the intervention. As a subanalysis the investigators will therefore analyse the interaction between MOD/non-MOD subgroup and exposure to the intervention using a linear model with a term for the cluster variable, a term for the exposure to the intervention and an interaction term.

• Study Type: Interventional
• Enrollment (Estimated): 300
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Sweden
  • Skane
    • Malmö, Skane, Sweden, 20502
      • Clinical Research Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 35 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Patients with type 2 diabetes at or above 35 years of age
• Diagnosis of diabetes mellitus was based on prior documentation or treatment with anti-hyperglycemic medication or diagnosed according to the WHO criteria (random plasma glucose >11.1 mmol/L or fasting glucose >7.0 mmol/L or HbA1C ≥6.5%).
• written informed consent.

Exclusion Criteria:

• type 1 diabetes, MODY or secondary diabetes
• conditions or treatments that in the judgement of the Investigator could affect the study evaluation
• inability to understand written Swedish
• connection with the study team, funders, authorities, universities or other public or private bodies in such a way that specific interests in the study outcomes could be suspected.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Access to tool; Access to the digital tool. They use the tool at their own and do the different themes that are available. They are recommended to use it at least every other week.	Behavioral: Health and lifestyle tool; Health and lifestyle tool used online
Placebo Comparator: Usual care; They are followed by their ordinary healthcare provider.	Other: Usual care; Usual care at ordinary healthcare provider

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change of long-term blood glucose concentration measured as glycated hemoglobin at 3 months	Intraindividual change of long-term blood glucose concentration measured as glycated hemoglobin (HbA1c) at 3 months relative to baseline compared between participants with access to the tool and on usual care.	3 months
Change of long-term blood glucose concentration measured as glycated hemoglobin at one year	Intraindividual change of long-term blood glucose concentration measured as glycated hemoglobin (HbA1c) at one year relative to baseline between participants who use the tool as recommended and matched controls on usual care	One year of the open-label observation period

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change of long-term blood glucose concentration measured as glycated hemoglobin at three years	Intraindividual change of long-term blood glucose concentration measured as glycated hemoglobin (HbA1c) at three years relative to baseline between participants who use the tool as recommended and matched controls on usual care	Three years of the open-label observation period
Body weight	Body weight between groups	3 months, 1 year and 3 years
Insulin resistance	Insulin resistance measured as HOMA-IR	3 months, 1 year and 3 years
Fasting blood glucose concentration	Fasting blood glucose concentration between groups	3 months, 1 year and 3 years
Physical activity in calories per day	Physical activity in calories per day estimated by International Physical activity questionnaire between users of the tool and controls on usual care. Score measures calorie consumption and ranges from 0 to unlimited	3 years
Insulin secretion	Insulin secretion estimated by HOMA-B	1 year and 3 years

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change of long-term blood glucose concentration measured as glycated hemoglobin in participants with and without Mild Obesity-related Diabetes, respectively.	As a subanalysis we will analyse the effect of the intervention specifically on patients with Mild Obesity-related Diabetes (MOD). This will be analysed by a formal interaction test between MOD and non-MOD participants exposed or not exposed to the intervention by using a linear model with a term for MOD/non-MOD, a term for the exposure/non-exposure to the intervention and an interaction term.	1 year and 3 years

Collaborators and Investigators

• Sponsor: Region Skane
• Investigators: Principal Investigator: Anders Rosengren, Region Skane

Publications and helpful links

General Publications

• Dwibedi C, Abrahamsson B, Rosengren AH. Effect of Digital Lifestyle Management on Metabolic Control and Quality of Life in Patients with Well-Controlled Type 2 Diabetes. Diabetes Ther. 2022 Mar;13(3):423-439. doi: 10.1007/s13300-022-01214-2. Epub 2022 Feb 12.

Study record dates

Study Major Dates

• Study Start (Actual): January 1, 2021
• Primary Completion (Estimated): December 31, 2026
• Study Completion (Estimated): December 31, 2026

Study Registration Dates

• First Submitted: October 30, 2020
• First Submitted That Met QC Criteria: November 5, 2020
• First Posted (Actual): November 10, 2020

Study Record Updates

• Last Update Posted (Actual): July 16, 2025
• Last Update Submitted That Met QC Criteria: July 13, 2025
• Last Verified: July 1, 2025

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Endocrine System Diseases; Metabolic Diseases; Glucose Metabolism Disorders; Diabetes Mellitus; Diabetes Mellitus, Type 2
• Other Study ID Numbers: Health1

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: Individual participant data that underlie the results will be shared after deidentification.
• IPD Sharing Time Frame: Data will be available after publication.
• IPD Sharing Access Criteria: To researchers who provide a methodologically sound proposal in order to achieve the aims of that proposal. Proposals should be directed by email to internetverktyg@gu.se

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No