Effectiveness and Theory-based Evaluation of a Personalised Digital Intervention (EviBody) for Healthy and Sustained Lifestyle Behaviours and Well-being Among Adults
Led by Sophiahemmet University · Updated on 2026-04-29
1500
Participants Needed
1
Research Sites
104 weeks
Total Duration
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AI-Summary
Brief Title
Who Can Participate
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Your Study Journey
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Sophiahemmet University
Lead Sponsor
K
Karolinska Institutet
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the impact of a personalized digital intervention called EviBody on well-being, lifestyle behaviors, and mental health in adults. This quasi-experimental observational study compares users of the EviBody app with a control group from the general population. The study aims to answer questions about the effectiveness of the digital support for healthy habits over 6 months and 24 months, and how factors like engagement and sociodemographics influence outcomes.
The study uses a four-armed design with three levels of the EviBody digital intervention—Basic, Standard, and Premium—and a control group without exposure. The app includes features for healthy eating, physical activity, and mental balance, such as tracking, goal setting, feedback, AI chat, recipe and exercise databases, and webinars. Higher membership levels offer social support and individual coaching via private online health consultations. Participants choose their membership level when enrolling.
Participants will complete seven questionnaires over two years and allow researchers to collect app usage data. The research will measure well-being at 6 and 24 months as primary outcomes, with secondary measures including stress, burnout, and sleep. The study will track how participants maintain healthy habits and mental health, and analyze patterns of user engagement, motivation, and perceived barriers during the 24-month period.
CONDITIONS
Brief Title
Evaluation of a Personalised Digital Intervention (EviBody) for Healthy and Sustained Lifestyle Behaviors and Well-being Among Adults: a Real-world Quasi-experimental Study
Who Can Participate
Age: 18Years +
All Genders
Healthy Volunteers
Eligibility Criteria
You may qualify if you...
Adults aged 18 years or older
Signing up for the EviBody app using electronic identification (intervention group)
Consent to participate in the research study
Adults aged 18 years or older (control group)
You will not qualify if you...
Individuals discharged from the app for violating terms of service (intervention group)
Currently using a digital product designed to support behavior change
Well-being score above 70 (excluded from primary analyses)
Friends, colleagues, or family of anyone in the research or owner group
Users of the EviBody app (control group)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Outpatient Treatment
Duration - Up to 24 months
Participants use the EviBody app tailored to their chosen membership level (Basic, Standard, or Premium) to support healthy eating, physical activity, and mental balance. This includes tracking behaviors, goal setting, action planning, feedback, digital rewards, AI chat, and access to resources such as recipes, exercises, and webinars. Some participants may receive social support and private online health consultations depending on their membership.
7 questionnaire assessments over 2 years
Long-term Monitoring
Duration - Up to 24 months
Participants' well-being, stress, burnout, and sleep are monitored through questionnaires and app data over the course of 24 months to evaluate the sustained impact of the digital intervention.
Data extracted continuously from app analytics; questionnaire assessments as scheduled
Effectiveness and theory-based evaluation of a personalised digital intervention (EviBody®) for healthy and sustained lifestyle behaviours and well-being among adults: Study protocol for a real-world quasi-experimental study.