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SMS-based telemedical after-care of patients of Jena University Hospital's Pain Day Clinic

Not Applicable
Completed
Conditions
F45.41
Registration Number
DRKS00008068
Lead Sponsor
niversitätsklinikum Jena
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
45
Inclusion Criteria

Intervention group:
- meeting inclusion criteria for multi-modal pain therapy
- informed consent
- availability of a mobile phone
- ability to read and write SMS
- knowledge of German language.

Comparison group:
- meeting inclusion criteria for multi-modal pain therapy
- informed consent

Exclusion Criteria

- not meeting one or more of the inclusion criteria

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Feasibility test of a telemedical intervention and its acceptance by the patient population. Acceptance is assessed by use of a patient questionnaire that will be completed 2 months after end of the telemedical intervention.
Secondary Outcome Measures
NameTimeMethod
2. change of pain intensity (assessed by use of BPI)<br>3. change of pain-caused impairments (assessed by use of Korff-scale)<br>4. change of health-related quality of life (assessed by use of SF-12)<br><br>Time of assessment: 4 weeks and 2 months after end of intervention
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