Complex Regional Pain Syndrome Clinical Trials

Find Complex Regional Pain Syndrome Clinical Trials Near You

Study of the Representation of Action Peripersonal Space in Participants With Unilateral Segmental Exclusion of the Upper Limb Compared to Asymptomatic Subjects

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Observational
SUMMARY

This study aims to evaluate the representation of action peripersonal space (PPS) in subjects suffering from unilateral segmental exclusion syndrome of the upper limb compared to healthy control subjects. Segmental exclusion is defined by non-use or under-use of a limb segment without central nervous system damage. The study hypothesizes that this syndrome leads to a modification (shrinkage) of the PPS representation. Participants will perform reachability judgments in a Virtual Reality (VR) environment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Age ≥ 18 years.

• Presenting unilateral exclusion symptom of the upper limb or part of the hand evolving for \> 3 months.

• No contraindication to force work in daily activities.

• For patients with finger exclusion: at least 2 perturbed items related to exclusion on tests 3 and 4 of the Bilan 400 points.

• Affiliated to a social security scheme.

• Able to understand simple orders.

• Age ≥ 18 years.

• No history of upper limb impairment with sequelae.

Locations
Other Locations
France
Institut Régional de Médecine Physique et de Réadaptation (IRR), Centre Louis Pierquin.
RECRUITING
Nancy
Contact Information
Primary
Amélie Touillet, MD
amelie.touillet@ugecam.assurance-maladie.fr
+33 3 83 52 98 80
Backup
Jonahtan Pierret, PhD
jonathan.pierret@ugecam.assurance-maladie.fr
+33 3 83 52 67 61
Time Frame
Start Date: 2025-12-04
Estimated Completion Date: 2028-01
Participants
Target number of participants: 60
Treatments
Patients with Exclusion
Patients presenting with unilateral segmental exclusion of the upper limb or part of the hand evolving for more than 3 months.
Healthy Controls
symptomatic volunteers with no history of upper limb impairment with sequelae.
Related Therapeutic Areas
Sponsors
Leads: Union de Gestion des Etablissements des Caisses d'Assurance Maladie - Nord Est

This content was sourced from clinicaltrials.gov