General Mental Health and Well-BeingPREWELLNCT07868146
PREWELL Digital Well-being Promotion Intervention With the BitHabit App
A study testing Digital wellbeing promoting intervention with the BitHabit app in people with General Mental Health and Well-Being and Mental Disorders, run by University of Eastern Finland at 1 site in Finland.
Trial summary
Mental wellbeing is a major public health concern, and digital interventions have emerged as a scalable approach for promoting mental well-being and healthy lifestyle behaviors. However, evidence regarding long-term effectiveness and the role of user engagement remains limited. Read more about this study
- Who is it for?
- Ages 18 to 64 yearsHealthy volunteers can take part
- Conditions the study is for
- General Mental Health and Well-Being, Mental Disorders, Common Mental Disorders (CMD)
- What is being tested?
- Digital wellbeing promoting intervention with the BitHabit app
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,700 participants
- Where
- 1 siteFinland
- Study dates
- 10 May 2024to 31 Dec 2035
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 to 64 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- age between 18 and 64 years
- living in North Savo, Finland
Who cannot join
- no access to personal mobile devices or to the internet
Trial locations and contacts
1 site in 1 country.
Finland1 site
University of Eastern Finland & Wellbeing Services County of North Savo
Kuopio, Northern Savonia, FI-70211
About this study
Official title: PREcision Promotion of Positive Mental WELLbeing Among High-risk Adult Population (PREWELL): Capabilities, Gamification, and Digital Intervention
Mental wellbeing is a major public health concern, and digital interventions have emerged as a scalable approach for promoting mental well-being and healthy lifestyle behaviors. However, evidence regarding long-term effectiveness and the role of user engagement remains limited. This study evaluates the effectiveness of the BitHabit digital wellbeing application in promoting mental wellbeing and healthy lifestyle among adults living in North Savo, Finland.
The BitHabit application is a digital behavior change intervention designed to support mental wellbeing through the adoption of small, self-selected wellbeing-promoting habits. The application incorporates principles of self-determination theory, habit formation, self-monitoring, and behavior change techniques. Participants select habits from a library of well-being-promoting activities and track their implementation over time.
Read more
The intervention study uses a stepped-wedge randomized controlled design in which all participants eventually receive access to the intervention, while participants awaiting access serve as controls. Adults aged 18 to 64 years living in North Savo were recruited between 2024 and 2025 through population registry sampling and open public recruitment. Following informed consent and baseline assessment, participants were randomly allocated to receive access to the intervention at different time points during the study.
Power calculations using Monte Carlo simulations indicated that approximately 1,600 participants would provide 80% power to detect a standardized mean difference of 0.30 in mental wellbeing (SWEMWBS), assuming four intervention sequences, five measurement occasions, a within-person intraclass correlation coefficient of 0.70, and 30% attrition.
The primary outcome mental wellbeing is assessed using the Short Warwick-Edinburgh Mental Wellbeing Scale (SWEMWBS). Secondary outcomes include depressive symptoms measured with the Patient Health Questionnaire (PHQ-9), self-reported capabilities, loneliness measured with the UCLA 3-item Loneliness Scale (UCLA-3), life satisfaction measured on a 0-10 scale, and self-reported health behaviours. Outcomes are measured at baseline and repeated follow-up assessments throughout the study. We hypothesize that participants receiving the intervention will show greater improvement in all primary and secondary outcome measures compared with the control condition. App usage data are used to evaluate intervention adoption and engagement and to examine whether effectiveness differs according to actual intervention use.
Statistical analyses will be conducted using mixed-effects regression models that account for the stepped-wedge design and repeated measurements within participants. Models will include fixed effects for intervention exposure and time, and a random intercept for participants. Estimates will be reported with 95% confidence intervals and a two-sided significance level of 0.05.
In addition to quantitative outcome assessments, participant experiences and acceptability of the intervention will be evaluated with user satisfaction questionnaires and qualitative interviews conducted among a subset of participants. These data will be used to assess perceived usefulness, user experiences, and opportunities for further development of the intervention.
In addition to questionnaire and app usage data, participants will be linked to regional and national administrative registers. Register-based follow-up covers the period from one year before study enrolment until up to ten years after study completion. Data sources include health and social care registers, prescription and reimbursement registers, employment-related registers, and population registers. These data will be used to evaluate the long-term effectiveness and cost-effectiveness of the intervention, including health service use, medication use, social outcomes, and associated costs.
- Being tested
- Digital wellbeing promoting intervention with the BitHabit app
- Keywords
- Mental health, Health promotion, Mobile applications, Health behavior, Self-management, Depression, Loneliness, Quality of life, Adults, Behavior Therapy, Lifestyle, Patient engagement, Preventive health services, Public health, Randomized controlled trial
- Medical subject headings
- Mental Disorders, Psychological Well-Being, Health Behavior, Depression, Patient Participation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Digital wellbeing promoting intervention with the BitHabit appBehavioural
The BitHabit intervention is a digital wellbeing application designed to support mental wellbeing through the adoption of small, self-selected wellbeing-promoting habits. Participants choose habits from a library covering areas such as physical activity, sleep, stress management, social relationships, recovery, and healthy daily routines. The intervention is based on self-determination theory, habit formation principles, and evidence-based behavior change techniques. Users can monitor their habit performance, receive reminders and notifications, and gradually integrate wellbeing-promoting behaviors into everyday life. Access to the intervention is provided through a web-based application and participants may continue using the application throughout the intervention period.
| Study group | Role | What they receive |
|---|---|---|
| Intervention | Experimental | Digital wellbeing promoting intervention with the BitHabit app Receives: Behavioral: Digital wellbeing promoting intervention with the BitHabit app |
| Control/Treatment as Usual | No intervention | Control group |
What is being measured
The primary outcome is the main question the study is designed to answer.
Short Warwick-Edinburgh Mental Well-Being Scale (SWEMWBS)
A self-reported validated measure of health and wellbeing measured with the Warwick-Edinburgh Mental Wellbeing Scale (Sarasjärvi et al 2025; Tennant et al 2007). Scores range from 7 to 35 and higher scores indicate higher positive mental wellbeing.
Measured: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.
Secondary outcomes (4)
PHQ-9 depression scale
Depressive symptoms were assessed using the validated 9-item Patient Health Questionnaire (PHQ-9), which measures the frequency of depressive symptoms during the past two weeks on a scale from 0 ("not at all") to 3 ("nearly every day"). Higher scores indicate greater depressive symptom severity.
Measured: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.
Self-reported capabilities
Validated self-report measure based on the Capability Approach (Mäki-Opas et al 2022). It assesses individuals' perceived opportunities and freedoms to achieve valued ways of living across multiple life domains, including health, social relationships, participation, security, and personal development. Single items are coded from 1 to 7, higher indicating better perceived capabilities.
Measured: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.
UCLA-3 short loneliness scale
Loneliness was measured using the three-item short form of the UCLA Loneliness Scale (UCLA-3), which assesses feelings of lacking companionship, being left out, and being isolated from others. Responses are rated on a three-point scale, with higher scores indicating greater loneliness.
Measured: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.
Life satisfaction
A single-item measure asking participants to rate their overall satisfaction with life on a scale from 0 to 10, where 0 indicates "completely dissatisfied" and 10 indicates "completely satisfied." Higher scores reflect greater subjective well-being and overall life satisfaction.
Measured: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Oct 2026
- Study start10 May 2024
- Primary completion31 Dec 2026 (estimated)
- Study completion31 Dec 2035 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for General Mental Health and Well-BeingStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Sequential
- Model description
- This study uses a stepped-wedge randomized controlled design in which all participants eventually receive the intervention. Participants were randomly assigned to one of four intervention sequences in two waves determining when access to the intervention was initiated. At each step, a proportion of participants transitioned from the control condition to the intervention condition, while participants awaiting intervention served as controls. Questionnaire data were collected at baseline and repeated follow-up assessments (request send every three months but respondents can also give follow-ups more often when they wish) throughout the study. This design enabled within- and between-participant comparisons of outcomes before and after intervention exposure while ensuring that all participants ultimately received access to the intervention.
- Masking
- None (open label)
- Enrolment
- 1,700 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Eastern Finland
- Sponsor type
- University, hospital or other
- Collaborators
- University of Bern, London School of Economics and Political Science, Wellpro Impact Solutions Ltd, Wellbeing Services County of North Savo
- Responsible party
- Principal investigator, Tomi Mäki-Opas, University of Eastern Finland
- Investigators
- Tomi E Mäki-Opas, Professor, Principal investigator, University of Eastern Finland & Wellbeing Services County of North Savo
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07868146
- Sponsor's protocol ID
- 844/13.00/2023
- Other IDs
- 363107
- Acronym
- PREWELL
- Status last verified
- Oct 2026
- First submitted
- 1 Oct 2026
- Last updated
- 29 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: We do not have permission to share IPD from the participants.
Study at a glance
From the registry record, last updated by the sponsor on 29 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- PREcision Promotion of Positive Mental WELLbeing Among High-risk Adult Population (PREWELL): Capabilities, Gamification, and Digital Intervention
- ClinicalTrials.gov ID
- NCT07868146
- Acronym / sponsor ID
- PREWELL / 844/13.00/2023
- Keywords
- Mental health, Health promotion, Mobile applications, Health behavior, Self-management, Depression, Loneliness, Quality of life
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 1,700 participants (actual)
- Lead sponsor
- University of Eastern FinlandUniversity, hospital or other
- Collaborators
- University of Bern, London School of Economics and Political Science, Wellpro Impact Solutions Ltd, Wellbeing Services County of North Savo
- Study start
- 10 May 2024 (actual)
- Primary completion
- 31 Dec 2026 (estimated)
- Study completion
- 31 Dec 2035 (estimated)
- First posted
- 9 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Mental wellbeing is a major public health concern, and digital interventions have emerged as a scalable approach for promoting mental well-being and healthy lifestyle behaviors. However, evidence regarding long-term effectiveness and the role of user engagement remains limited. This study evaluates the effectiveness of the BitHabit digital wellbeing application in promoting mental wellbeing and healthy lifestyle among adults living in North Savo, Finland.
The BitHabit application is a digital behavior change intervention designed to support mental wellbeing through the adoption of small, self-selected wellbeing-promoting habits. The application incorporates principles of self-determination theory, habit formation, self-monitoring, and behavior change techniques. Participants select habits from a library of well-being-promoting activities and track their implementation over time.
The intervention study uses a stepped-wedge randomized controlled design in which all participants eventually receive access to the intervention, while participants awaiting access serve as controls. Adults aged 18 to 64 years living in North Savo were recruited between 2024 and 2025 through population registry sampling and open public recruitment. Following informed consent and baseline assessment, participants were randomly allocated to receive access to the intervention at different time points during the study.
Power calculations using Monte Carlo simulations indicated that approximately 1,600 participants would provide 80% power to detect a standardized mean difference of 0.30 in mental wellbeing (SWEMWBS), assuming four intervention sequences, five measurement occasions, a within-person intraclass correlation coefficient of 0.70, and 30% attrition.
The primary outcome mental wellbeing is assessed using the Short Warwick-Edinburgh Mental Wellbeing Scale (SWEMWBS). Secondary outcomes include depressive symptoms measured with the Patient Health Questionnaire (PHQ-9), self-reported capabilities, loneliness measured with the UCLA 3-item Loneliness Scale (UCLA-3), life satisfaction measured on a 0-10 scale, and self-reported health behaviours. Outcomes are measured at baseline and repeated follow-up assessments throughout the study. We hypothesize that participants receiving the intervention will show greater improvement in all primary and secondary outcome measures compared with the control condition. App usage data are used to evaluate intervention adoption and engagement and to examine whether effectiveness differs according to actual intervention use.
Statistical analyses will be conducted using mixed-effects regression models that account for the stepped-wedge design and repeated measurements within participants. Models will include fixed effects for intervention exposure and time, and a random intercept for participants. Estimates will be reported with 95% confidence intervals and a two-sided significance level of 0.05.
In addition to quantitative outcome assessments, participant experiences and acceptability of the intervention will be evaluated with user satisfaction questionnaires and qualitative interviews conducted among a subset of participants. These data will be used to assess perceived usefulness, user experiences, and opportunities for further development of the intervention.
In addition to questionnaire and app usage data, participants will be linked to regional and national administrative registers. Register-based follow-up covers the period from one year before study enrolment until up to ten years after study completion. Data sources include health and social care registers, prescription and reimbursement registers, employment-related registers, and population registers. These data will be used to evaluate the long-term effectiveness and cost-effectiveness of the intervention, including health service use, medication use, social outcomes, and associated costs.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- This study uses a stepped-wedge randomized controlled design in which all participants eventually receive the intervention. Participants were randomly assigned to one of four intervention sequences in two waves determining when access to the intervention was initiated. At each step, a proportion of participants transitioned from the control condition to the intervention condition, while participants awaiting intervention served as controls. Questionnaire data were collected at baseline and repeated follow-up assessments (request send every three months but respondents can also give follow-ups more often when they wish) throughout the study. This design enabled within- and between-participant comparisons of outcomes before and after intervention exposure while ensuring that all participants ultimately received access to the intervention.
| Arm | Type | Receives |
|---|---|---|
| Intervention | Experimental | Behavioral: Digital wellbeing promoting intervention with the BitHabit appDigital wellbeing promoting intervention with the BitHabit app |
| Control/Treatment as Usual | No intervention | –Control group |
Who may qualify
- Ages
- 18 to 64 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- age between 18 and 64 years
- living in North Savo, Finland
Key exclusion criteria (1 listed)
- no access to personal mobile devices or to the internet
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Digital wellbeing promoting intervention with the BitHabit appThe BitHabit intervention is a digital wellbeing application designed to support mental wellbeing through the adoption of small, self-selected wellbeing-promoting habits. Participants choose habits from a library covering areas such as physical activity, sleep, stress management, social relationships, recovery, and healthy daily routines. The intervention is based on self-determination theory, habit formation principles, and evidence-based behavior change techniques. Users can monitor their habit performance, receive reminders and notifications, and gradually integrate wellbeing-promoting behaviors into everyday life. Access to the intervention is provided through a web-based application and participants may continue using the application throughout the intervention period. | Behavioural | Intervention |
Primary outcome
Short Warwick-Edinburgh Mental Well-Being Scale (SWEMWBS)
Time frame: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.
A self-reported validated measure of health and wellbeing measured with the Warwick-Edinburgh Mental Wellbeing Scale (Sarasjärvi et al 2025; Tennant et al 2007). Scores range from 7 to 35 and higher scores indicate higher positive mental wellbeing.
4 secondary outcomes
PHQ-9 depression scale
Time frame: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.
Self-reported capabilities
Time frame: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.
UCLA-3 short loneliness scale
Time frame: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.
Life satisfaction
Time frame: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Oct 2026.
- PREWELL www-pageLink provided by the sponsor.
- Individual participant dataSharing planned: No. We do not have permission to share IPD from the participants.
Related trials for General Mental Health and Well-Being
Recruiting
Effect of a Brief Daily Digital Meditation on Well-Being in US Young Adults (BEGIN II)
Mental Health and General Well-being
Active, not recruiting
Future School of Comprehensive Well-Being
Learning, Comprehensive Wellbeing
Not yet recruiting
CannaRiver CBD Calm for Anxiety, Sleep, and Well-Being in Adults With Generalized Anxiety Disorder
Generalized Anxiety Disorder
Not yet recruiting
QAIAx - SGI/SI Smart Health Cities: Microcity Enclave Program (Quantum SI/AGI Agency a/k/a AI City Hall Project - UPSTO App Nos. 64/074,526, 64/063,557, 64/105,164, 63/903,181, 63/729,428, 64/125,360; USPTO EO 9424 Assignment ID: 2101042 / ARN: REEL/FRAME: 76481/0026 - OUSD-R&E, Department of War)
Asperger's Disorder, Asperger Disorder
Not yet recruiting
Miles for Mental Health
Generalized Anxiety Disorder (GAD), Depressive and Anxiety Disorders
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Tomi E Mäki-Opas, Professor principal investigator
University of Eastern Finland & Wellbeing Services County of North Savo
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Digital wellbeing promoting intervention with the BitHabit app in people with General Mental Health and Well-Being and Mental Disorders, run by University of Eastern Finland at 1 site in Finland.
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 2 inclusion and 1 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: under way, not looking for participants, as of the sponsor's last update on 29 Oct 2026. 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 Finland. 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?
This study is still under way. Results are not available in the source record yet.
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?
Short Warwick-Edinburgh Mental Well-Being Scale (SWEMWBS) (time frame: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.). 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 29 Oct 2026.