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Evaluation of a new treatment concept for short-term care in rehabilitation facilities for internal diseases- StarK.

Not Applicable
Conditions
N17.9
I73
I74
R68.8
R65
I25.5
I50
I42
I11
T98.3
Registration Number
DRKS00025393
Lead Sponsor
Institut für Rehabilitationsmedizinische Forschung an der Universität Ulm
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
50
Inclusion Criteria

Insured persons of AOK-BW
- AOK-BW is the responsible rehabilitation provider
- Recognizable motivation
- Exclusion of dementia
- negative COVID test on admission
- Exclusion of multi-resistant germs
- acute medical treatment must be completed
- central i.V. Accesses must be removed
- Drains of large body cavities must be removed
- Partial mobilization and room mobility must be available
- Exclusion of urinary and fecal incontinence

Exclusion Criteria

- Premorbid geriatric multimorbidity
- Insufficient knowledge of German
- Existing rehabilitation capability
- Existing level of care

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Intervention group: <br>Measured by written survey (questionnaire).<br>Measurement time points: (admission (t1) and end of short-term rehabilitative care (t2)). <br><br>Primary endpoints are the acceptance of and satisfaction with the StarK intervention, the rate of patients who did not start or prematurely discontinued the AHB<br>and the survey of interface problems.
Secondary Outcome Measures
NameTimeMethod
Secondary endpoints will be assessed using focus groups by participating professions at the rehabilitation facility, as well as interviews with participating staff at the acute care hospitals. <br><br><br>Secondary endpoints: Potential for improvement regarding the process of the intervention, suggestions for improvement with regard to the designed checklist, and review of the referred target group or adjustment of the inclusion/exclusion criteria.
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