Z89
Conditions
Interventions
Group 1: People in study arm 1 (intervention) will already be accompanied by a care manager during their acute phase in hospital, who supports the patients and coordinates the treatment procedures. Th
Sponsors
Klinik für Rehabilitationsmedizin, Medizinische Hochschule Hannover
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Major-Amputation (OPS 5-864.0 bis 5-865.3) on one of the lower limbs, able to walk before amputation
Exclusion criteria
Exclusion criteria: double-sided amputation; amputation performed outside of Germany
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome is the physical functioning. It will be measured at four different moments during the questionnaire (t1= before rehabilitation, t2= after rehabilitation, t3= 6 month after amputation, t4= 12 month after amputation) using the scale "physical functioning". | — |
Secondary
| Measure | Time frame |
|---|---|
| The following secondary outcomes will be assessed by questionnaire before follow-up rehabilitation, at the end of rehabilitation and at 6-month follow-up and 12-month follow-up: social participation (IMET), work-ability (WAI), health-related quality of life (COPSOQ), mobility, pain (GCPS), anxiety and depression (PHQ-4), as well as satisfaction with prosthetic care (ZUF-8). | — |
Countries
Germany
Contacts
Public ContactStella Lemke
Universität zu LübeckInstitut für SozialmedizinArbeitsgruppe Rehabilitation & Arbeit
Outcome results
None listed