MedPath

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

Not Applicable
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
© Copyright 2025. All Rights Reserved by MedPath