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TerminatedNCT03386188CORTEXUpdated Apr 22, 2026

Role of the Posterior Parietal Cortex in the Processing of Sensory Information

An interventional study of Transcranial Magnetic Stimulation (TMS) and Electrical Muscle Activity (EMG) in Healthy Subject, sponsored by University Hospital, Lille. Terminated at 1 site in France. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-22.

Sponsored by University Hospital, Lille · Not applicable, Interventional, and Basic science

Why this study was terminated
sponsor decision
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years to 40 Years
Sex
All
01

Study summary

Although the primary motor cortex is considered has the common final pathway of motor commands, it is influenced by several structures as, for example, the premotor cortex and the posterior parietal cortex which are involved in motor planning and programming and which integrates movement-induced sensory impute (parieto-frontal circuits). Several studies have shown that there are some direct functional connections between the premotor cortex and the posterior parietal cortex and from these two regions to the primary motor cortex. The posterior parietal cortex can then be considered as a sensorimotor interface whose function in planification and motor control of upper limb is well demonstrated. The hypothesis is that the posterior parietal cortex could participate to the modulation of motor cortex excitability by proprioceptive sensory inputs namely long latency afferent inhibition and afferent induced facilitation.

02

Conditions studied

  • Healthy Subject
03

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Right handed
  • No neurological troubles
  • Informed consent signed
  • Affiliated to a social security

Exclusion criteria

Exclusion Criteria:

  • Psychiatric antecedent
  • Neurological disease
  • Contra-indication to TMS
  • Under psychiatric treatment
  • Pregnancy
  • Contra-indication to MRI
04

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    Healthy arm

    posterior parietal cortex (PPC) transitory inactivation

    Device: Transcranial Magnetic Stimulation (TMS) · Device: Electrical Muscle Activity (EMG)

Interventions

  • DeviceTranscranial Magnetic Stimulation (TMS)

    Transitory inactivation of the posterior parietal cortex and measure of sensorimotor integration.

  • DeviceElectrical Muscle Activity (EMG)

    Electrodes for the collection of EMG activity will be glued on the skin next to the first interosseus dorsalis muscle, the Abductor digiti minimi, the Extensor carpi radialis and the Abductor pollicis brevis. EMG signals will be stored on computer for off-line analysis using Signal © software (Cambridge Electronic Design, Cambridge, UK)

05

What researchers measure

Primary outcomes

  1. Afferent induced facilitation

    Motor cortex facilitation following median nerve stimulation at interstimulus intervals of 70ms

    Time frame: Baseline

Secondary outcomes

  1. Interaction between long latency afferent inhibition and long latency intracortical inhibition (LICI)

    Effect of median nerve stimulation on LICI at 100ms interval

    Time frame: Baseline

06

Study locations

1 site
  • Hôpital Roger Salengro, CHRU de Lille
    Lille, France
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03386188
Lead sponsor
University Hospital, Lille
Responsible party
Sponsor
First posted
Dec 29, 2017
Start date
Jan 8, 2016
Primary completion
Jul 18, 2021
Completion
Jul 18, 2021
Last update
Apr 22, 2026

Study contacts

Philippe Derambure, MD, PhD
principal investigator · University Hospital, Lille

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

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