Skip to content

Adaptation and evaluation of an mHealth tool to improve knowledge on dementia prevention and support behavior change to reduce dementia risk (“MyBraincoach.de”) in middle-aged and older adults in Germany

Adaptation and evaluation of an mHealth tool to improve knowledge on dementia prevention and support behavior change to reduce dementia risk (“MyBraincoach.de”) in middle-aged and older adults in Germany - MyBraincoach.de

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00038349
Enrollment
75
Registered
2025-11-03
Start date
2026-11-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy ageing, health promotion and prevention

Interventions

Group 1: Arm 1: independent use of the MyBrainCoach app over a three month-period •Download the app, log in •Complete the LIBRA assessment to identify modifiable risk factors for dementia (three cate
2) factors that cannot be directly influenced, e.g. diabetes mellitus, which should continue to be monitored/ treated
3) applicable risk factors that can be directly influenced (“room for improvement”)) •Independent selection of a risk/ protective factor •Receive daily notifications/ micro-teaching content on the se

Sponsors

Universität Leipzig, Medizinische Fakultät, Institut für Sozialmedizin, Arbeitsmedizin und Public Health
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: signed consent form (online); sufficient knowledge of German; ownership of a smartphone; internet access

Exclusion criteria

Exclusion criteria: no signed consent form; insufficient knowledge of German; no ownership of a smartphone; no internet access; serious illness that could jeopardize safe participation in the study; ongoing participation in other intervention studies on healthy ageing

Design outcomes

Primary

MeasureTime frame
Pilot study without primary endpoint. Target parameters: •Practicability of recruitment, number of participants at follow-up (12 weeks after study start) •App usage (number of downloads, number of modules used, and notifications received) •Use •Usability •Changes in modifiable risk factors for dementia •Changes in knowledge about modifiable risk factors for dementia •Health -related quality of life •Self-efficacy •Motivation to change behavior

Secondary

MeasureTime frame
Pilot study without secondary outcome, see “primary endpoint”

Countries

Germany

Contacts

Public ContactAndrea Zülke

Universität Leipzig, Medizinische Fakultät, Institut für Sozialmedizin, Arbeitsmedizin und Public Health

andrea.zuelke@medizin.uni-leipzig.de+49 341 97 15483

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Sep 18, 2026