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Virtual Reality in the Rehabilitation in Patients With Lower Limb Amputation.

U

University Hospital Erlangen

Status

Enrolling

Conditions

Rehabilitation
Lower Limb
Lower Extremity
Amputation
Activities of Daily Living
Virtual Reality

Treatments

Device: virtual reality rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT05773560
VR-amputation

Details and patient eligibility

About

The goal of this clinical trial is to test the impact of virtual reality on rehabilitation for the patients after a major amputation.

The main questions it aims to answer are:

  • Does the virtual-reality-assisted rehabilitation improve the life quality of patients (i.e. lesser pain, better spirit)?
  • Does the virtual-reality-assisted rehabilitation improve the daily life function of the patients? Participants will received a virtual-reality-assisted rehabilitation on the second postoperative day for ten days. The rehabilitation would be carried out two times per day and 30 minutes per training.

Full description

Despite the increasing development of revascularisation techniques, lower limb amputation often represent the last chance of survival for the vasculopathic patient with chronic limb threatening ischemia (CLTI). First goal after lower limb amputation is represented by a rapid prosthesis application. The patient in the immediate post-operative period must undergo intensive rehabilitation and physiotherapy, which involves not only a physical but also a psychological approach.

"Classical" recovery following lower limb amputation includes adequate pain therapy and physiotherapy to regain independence, strength, mobility and finally prothesis application to improve quality of life and restore mobility. The aim of this study is to investigate the effect of adding virtual reality to traditional rehabilitation following a lower limb amputation in patients due to limited circulation, with particularly attention to a possible improvement of psychological state, reduction of post-operative pain and more rapid improvement in regaining functional mobility

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • > 18 years
  • critical limb ischemia or acute limb ischemia
  • amputation above/below knee
  • unilateral lower limb amputees

Exclusion criteria

  • physical disability (paralysis, plegia)
  • inability to give informed consent
  • neurological or psychiatric problem that reduces compliance
  • loss of planned post-operative assessments
  • traumatic amputation in a patient without circulatory disorders

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Patients receiving rehabilitation with virtual reality.
Experimental group
Description:
Single Group Assignment Patients after a major amputation would received at least 10 days of rehabilitation with the assistance of virtual reality. Before the operation, patients consent, life quality, pain score and motivation score were be evaluated. The rehabiliation with virtual reality started on the second postoperative day. The pain score would be evaluated everyday before and after the rebilitation. On the fifth and tenth day, motivation, life quality and functional index would be carried out again as the evaluation of the outcome of training.
Treatment:
Device: virtual reality rehabilitation

Trial contacts and locations

1

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Central trial contact

Ulrich Rother, PD Dr. med.; Werner Lang, Prof. Dr. med.

Data sourced from clinicaltrials.gov

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