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Active, not recruitingNCT07868146PREWELLUpdated Oct 9, 2026

PREWELL Digital Well-being Promotion Intervention With the BitHabit App

An interventional study of Digital wellbeing promoting intervention with the BitHabit app in General Mental Health and Well-Being, Mental Disorders and Common Mental Disorders (CMD), sponsored by University of Eastern Finland. Active, not recruiting at 1 site in Finland. Open to participants aged 18 Years to 64 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by University of Eastern Finland · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 2 years 4 months after the study started (first participant enrolled May 2024, registered Oct 2026).
Updated Oct 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
1,700
Allocation
Randomized
Ages
18 Years to 64 Years
Sex
All
01

Study 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. 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. 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.

02

Conditions studied

  • General Mental Health and Well-Being
  • Mental Disorders
  • Common Mental Disorders (CMD)

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
03

In context

Mental Disorders

2,148 studies on the registry are indexed under Mental Disorders; 425 are open to participants now.

This study's enrollment of 1,700 is above the median of 96 across 1,607 interventional studies indexed under Mental Disorders.

Browse Mental Disorders studies →

Lead sponsor

University of Eastern Finland is the lead sponsor of 53 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 64 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • age between 18 and 64 years
  • living in North Savo, Finland

Exclusion criteria

Exclusion Criteria:

  • no access to personal mobile devices or to the internet
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
1,700 participants (actual)

Study arms

  • Experimental
    Intervention

    Digital wellbeing promoting intervention with the BitHabit app

    Behavioral: Digital wellbeing promoting intervention with the BitHabit app

  • No intervention
    Control/Treatment as Usual

    Control group

Interventions

  • BehavioralDigital wellbeing promoting intervention with the BitHabit app

    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.

06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.

Secondary outcomes

  1. 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.

    Time frame: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.

  2. 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.

    Time frame: At baseline, 3 months, 6 months, 9 months, 12 months and 24 months.

07

Study locations

1 site
  • University of Eastern Finland & Wellbeing Services County of North Savo
    Kuopio, Northern Savonia FI-70211, Finland
08

References and documents

Individual participant data

Plan to share: No — We do not have permission to share IPD from the participants.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started May 2024 (actual). Primary completion is estimated for Dec 2026, 31 months after the start.

Of 841 non-industry interventional studies with no phase under Mental Disorders, half reached primary completion within 29 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 45. This study's planned 31 months is close to that.

Counting every sponsor, half of 856 studies reached it within 29 months; a quarter within 13 and three quarters within 45.

Mental Disorders covers many different conditions, not one, so the studies compared here vary widely. Read these figures as a rough guide.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 1, 2026
First posted
Oct 9, 2026
StartActual
May 10, 2024
Primary completionEst.
Dec 31, 2026
CompletionEst.
Dec 31, 2035
Last update
Oct 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 9, 2026
Show all 1 update
  1. Oct 9, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07868146
Lead sponsor
University of Eastern Finland
Collaborators
University of Bern, London School of Economics and Political Science
Responsible party
Tomi Mäki-Opas (Professor, social and public policy, University of Eastern Finland) — Principal investigator
First posted
Oct 9, 2026
Start date
May 10, 2024
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2035 (estimated)
Last update
Oct 9, 2026

Study contacts

Tomi E Mäki-Opas, Professor
principal investigator · University of Eastern Finland & Wellbeing Services County of North Savo

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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