Practicability and effectiveness of a digitalised prevention programme
Phase 2
- Conditions
- 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)
- Registration Number
- DRKS00022550
- Lead Sponsor
- Knappschaft Kliniken Service GMBH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 245
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
Lack of basic knowledge of German language
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The study includes 3 measuring points:<br>1) t0 takes place during the stay at the prevention clinic and measures the initial conditions.<br>2) t1 takes place 12 weeks after the start of the intervention.<br>3) t2 takes place 24 weeks after the start of the intervention. (At the end of the intervention)<br><br>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 Outcome Measures
Name Time Method 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.