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Segmental Exclusion of the Upper Limb and Peri-personal Space

Segmental Exclusion of the Upper Limb and Peri-personal Space

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04778111
Acronym
EPPEX
Enrollment
30
Registered
2021-03-02
Start date
2021-05-02
Completion date
2021-12-31
Last updated
2022-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients With Musculoskeletal Disorders of the Upper Limb With Symptoms of Exclusion

Brief summary

This study is based on previous studies on the search of the limit of the peri-personal space. In a previous study, Gouzien et al. (2017) evaluated the peri-personal space of action of patients with upper limb amputations and sought a link between this space and the level of integration of their myoelectric prosthesis. We have decided to implement part of this protocol to evaluate the peri-personal space for another population with upper limb patholog: segmental exclusion of the upper limb. Exclusion is a phenomenon that is very little studied but known to orthopedic surgeons and physical medicine and rehabilitation physicians. It is characterized by the non-use or underuse of a limb segment in the absence of central nervous system involvement. This phenomenon is compared to peripheral neglect. Most of the time, the patient is unaware of his disorder he forgets his finger without realizing it, but this phenomenon can be reversible under verbal exhortation from a third party. The aim of this study is to observe if there is a change in peri-personal space in patients with unilateral segmental exclusion.

Interventions

OTHERMeasurement of the actual and perceived maximum reachable distance

A device (a table) will present luminous targets (green circles) to the subjects. Subjects will be asked to determine whether or not they are able to reach this target with their upper limb.

Sponsors

Union de Gestion des Etablissements des Caisses d'Assurance Maladie - Nord Est
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adult (age greater than or equal to 18 years old). * Person with a symptom of unilateral exclusion. * Person with no contraindication to hard work in activities of daily living due to the lesions. * Person who has given informed consent.

Exclusion criteria

* Person under 18 years of age. * Person with visual impairment * A person with a central neurological pathology. * A person with cognitive impairment related to a brain injury, psychiatric illness or intellectual disability. * A person who has difficulty understanding instructions. * A person of full age who is subject to a legal protection measure or who is unable to give consent.

Design outcomes

Primary

MeasureTime frameDescription
Delta-MRDDuring one evaluation sessionDifference (in cm or in % of error) between actual maximum reachable distance and perceived maximum reachable distance

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026