Healthy adults
Conditions
Interventions
Group 1: Healthy adults are recruited. After a baseline survey of primary and secondary patient-reported outcomes (e.g. well-being, body weight), participants receive access to the ChatBot-based lifes
Sponsors
Carl Gustav Carus Universitätsklinikum, Technische Universität Dresden
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: . Participant at least 18 years old · Capable of understanding and communicating in German · Participant willing to wear a wearable · Participant willing to use a ChatBot to track and communicate about their lifestyle · Participant with internet access and a computer and/or smartphone compatible with the ChatBot · Digital literacy to use a smartphone adequately and willingness to use it for their Well-being · Sufficient understanding of user interface (UI) of the Lifestyle-ChatBot · Participant willing and able to comply with all scheduled visits and other study procedures · Participant capable of giving personal informed consent
Exclusion criteria
Exclusion criteria: - Participant using other Apps or participating in other programs for improving their lifestyle · Participant with impairments – including mental or psychic impairments – or conditions which, in the opinion of the investigator, would seriously compromise the integrity of the study · Participant under 18 years of age · Participant using an insulin pump or continuous glucose monitoring (CGM)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoints are the change in general well-being (measured with the Who-5 questionnaire) and physical activity (expressed as daily step count, measured via the Garmin Smartwatch) after 1 months of using VitaLo. For this the WHO-5 questionnaire will be accessed at baseline and after 30 days. The daily step count will be assessed continuously over the 30-days study period. | — |
Secondary
| Measure | Time frame |
|---|---|
| - acceptance and usability of the VitaLo measured with the user experience questionnaire (UEQ) and usage data of VitaLo further exploratory endpoints - lifestyle data generated by the GARMIN device (e.g. sleep data, heart frequency) - patient-reported outcomes like body weight, self-efficacy and physical activity questionnaire (Messung der Sport- und Bewegungsaktivität; BSA) | — |
Countries
Germany
Contacts
Public ContactPeter Schwarz
Carl Gustav Carus Universitätsklinikum, Technische Universität Dresden
Outcome results
None listed