NCT03286686

Brief Summary

To produce hand's movement directed towards a target, the investigator must combine several sensory information, such as vision or proprioception. The posterior parietal cortex (PPC) is a region of the cortex involved in this multisensory integration. A lesion of the PPC cause a visuo-motor trouble called optic ataxia but these patients also have perceptual troubles. The aim of the study is to understand the different functions of the PPC and especially how the processes of spatial coding of the sensory information influences perception and motor planning. In this study, the investigator want to explore the sensory motor and the perceptual performance of patients with optic ataxia compared with healthy subjects, using 6 behavioral tests. Objectify the consequences of PPC impairment (visual-motor and perceptual consequences) on patients' quality of life and autonomy.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
160

participants targeted

Target at P75+ for not_applicable healthy-volunteers

Timeline
58mo left

Started Feb 2018

Longer than P75 for not_applicable healthy-volunteers

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress63%
Feb 2018Feb 2031

First Submitted

Initial submission to the registry

September 14, 2017

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 18, 2017

Completed
5 months until next milestone

Study Start

First participant enrolled

February 22, 2018

Completed
13 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 22, 2031

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 22, 2031

Last Updated

January 20, 2026

Status Verified

January 1, 2026

Enrollment Period

13 years

First QC Date

September 14, 2017

Last Update Submit

January 16, 2026

Conditions

Keywords

optic ataxiaposterior parietal cortex functionsmultisensory integration

Outcome Measures

Primary Outcomes (3)

  • response error - number of pointing error

    Day 0 after each stimulation

  • response error -measure of reaction times

    Day 0 after each stimulation

  • response error - percentage of right responses

    Day 0 after each stimulation

Study Arms (6)

Experience 1

EXPERIMENTAL
Behavioral: point targets

Experience 2

EXPERIMENTAL
Behavioral: point targets

Experience 3

EXPERIMENTAL
Behavioral: tactile stimulation

Experience 4

EXPERIMENTAL
Behavioral: visual images

Experience 5

EXPERIMENTAL
Behavioral: visual images

Experience 6

EXPERIMENTAL
Behavioral: visual images

Interventions

point targetsBEHAVIORAL

In the experiences 1 and 2, the participant needs to point different visual targets (LED) in the dark.

Experience 1Experience 2

In the experience 3, a tactile stimulation is applied to the middle finger of the 2 hands. The participant needs to indicate into a microphone when he feels the stimulation.

Experience 3
visual imagesBEHAVIORAL

Target dots or visual images are presented on a computer screen. The participant is required to point to the targets or to react as soon as possible by pressing a response button when they are detected.

Experience 4Experience 5Experience 6

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • All patients and healthy subjects:
  • male and female, age from 18 to 75 years included
  • normal vision or corrected vision
  • covered by social security
  • signed written informed consent
  • Patients:
  • neurological injury in posterior parietal cortex supported by a cerebral MRI
  • present optic ataxia symptoms Healthy subjects
  • no known neurological injury

You may not qualify if:

  • \- unable to comply with the tasks (neurological, psychiatric, sensory or motor troubles)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

U1028 INSERM - CNRS UMR 5292 Equipe ImpAct

Bron, 69500, France

RECRUITING

Study Officials

  • Laure PISELLA, PhD

    INSERM U1028 - Impact - CRNL

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Laure PISELLA, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 14, 2017

First Posted

September 18, 2017

Study Start

February 22, 2018

Primary Completion (Estimated)

February 22, 2031

Study Completion (Estimated)

February 22, 2031

Last Updated

January 20, 2026

Record last verified: 2026-01

Locations