Pain complaints in the area of the locomotor body parts (e.g., back) Health impairments of the inner organs (e.g. high blood pressure, obesity) Mental impairments (e.g., occupational overload, stress) Individual risk factors like smoking, poor eating habits, lack of physical activity or obesity) Poor work conditions (e.g. stress because of shift work, work density, performance pressure, noise, cold, heat, monotonous body posture)
Conditions
Interventions
Group 1: Digital prevention - intervention group (Caspar)
After a two-weeks stay at the rehabilitation centre, persons will be supervised by the digital platform Caspar for six months.
Group 2: Traditional prevention - control grup (Betsi)
Persons take part in the traditional prevention program Betsi (RV Fit). See here https://www.azr.de/ambulante-gesundheitsfoerderung/praeventionsmassnahme-der-rentenversicherung/
Sponsors
Knappschaft Kliniken Service GMBH
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: The following CAN characteristics distinguish the target group: - Healthy test persons with a claim to prevention - Pain complaints in the area of the movement organs (e.g. back) - Health impairments of the internal organs (e.g. high blood pressure, overweight) - Psychological impairments (e.g. excessive demands at work, stress) - Individual risk factors (e.g. smoking, poor diet, lack of exercise) - unfavourable working conditions (e.g. shift work, monotonous posture, noise, cold, etc.)
Exclusion criteria
Exclusion criteria: Lack of basic knowledge of German language
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The study includes 3 measuring points: 1) t0 takes place during the stay at the prevention clinic and measures the initial conditions. 2) t1 takes place 12 weeks after the start of the intervention. 3) t2 takes place 24 weeks after the start of the intervention. (At the end of the intervention) At all three measurement points, work ability (WAI), subjective health (SF-12) and motivation (BREQ-2) are measured. In addition, the drop-out rate in the intervention and control group is measured from measurement time t1. | — |
Secondary
| Measure | Time frame |
|---|---|
| The study also includes interviews with different groups of probands - patients and therapists - which are conducted between t0 and t2 with the aim of exploring the user-friendliness, practicability and acceptance of the users. | — |
Countries
Germany
Contacts
Public ContactJulian Fritsch
Karlsruher Institut für TechnologieInstitut für Sport und Sportwissenschaft
Outcome results
None listed