Evaluation: Development and Implementation of a multimodal, cross-sectoral and cross-provider based care concept for major amputatio

Not Applicable

• Conditions: Z89; Acquired absence of limb

• Registration Number: DRKS00014664
• Lead Sponsor: Klinik für Rehabilitationsmedizin, Medizinische Hochschule Hannover

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-09-27
• Study Completion: 2021-12-31
• Results First Posted: 2023-01-24
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 40

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

double-sided amputation; amputation performed outside of Germany

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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).<br>