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Clinical Trials/NCT05931198
NCT05931198
Recruiting
N/A

Incorporation de prothèses Chez Les Patients amputés de Membre supérieur à l'IRMA

Institut Robert Merle d'aubigné1 site in 1 country36 target enrollmentSeptember 12, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Appropriate Affect
Sponsor
Institut Robert Merle d'aubigné
Enrollment
36
Locations
1
Primary Endpoint
Proprioceptive drift
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this observational study is to compare the strength of the incorporation according to the type of prosthesis (aesthetic, mechanical, myoelectric) with the experience the illusion of the rubber hand. The investigators will replace is the rubber by the patient's prothesis. The population will be people with upper arm amputation above the hand and they will be their own comparation.

Participants will do the the experience the illusion of the rubber hand in asynchronic and synchronic way and to answer questionnaries.

Registry
clinicaltrials.gov
Start Date
September 12, 2023
End Date
June 1, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Institut Robert Merle d'aubigné
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • At least one upper limb amputation
  • Informed and consented to participate to the study

Exclusion Criteria

  • having a history of severe neurological, visual or musculoskeletal impairments (other than the loss of a limb)
  • with severe serious psychiatric disorders (e.g. schizophrenia)
  • having problems understanding French in order to guarantee a good understanding of the questionnaires
  • under guardianship or curatorship

Outcomes

Primary Outcomes

Proprioceptive drift

Time Frame: Immediately after the intervention

Before and after each intervention, we are going to ask to the patient to point where we touch the residual limb on a graduated board.

Secondary Outcomes

  • Influence of patient's characteristic(During the patient's inclusion / Baseline)
  • Appropriate affect(Immediately after the intervention)

Study Sites (1)

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