Skip to main content
Clinical Trials/NCT05808504
NCT05808504
Recruiting
Not Applicable

Investigation of the Benefits of Electrical Non-invasive Stimulation on Cognitive Symptoms in Parkinson's Disease

Institut National de la Santé Et de la Recherche Médicale, France1 site in 1 country90 target enrollmentMay 3, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parkinson Disease
Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Enrollment
90
Locations
1
Primary Endpoint
Difference in cognitive performance measured by the stop signal reaction time (SSRT) compared between real and sham stimulation conditions
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Parkinson's disease is the second most common neurodegenerative disease after Alzheimer's disease.

It is mostly characterized by the presence of motor difficulties. However, it can also be accompanied by cognitive disorders which have an equally significant impact on the quality of life of patients and which are not relieved by any treatment.

Among the functions affected by Parkinson's disease, inhibition is an essential process for adapting our behaviors in daily life. Inhibition allows us to stop an action that is no longer required or appropriate to the situation in which we find ourselves in. For example, it comes into play when we have to stop at a "stop" sign while driving.

Recent studies suggest that it could be possible to improve the functioning of these processes by using non-invasive brain stimulation tools. Transcranial alternating current electrical stimulation has thus showed promising results in improving functions such as working memory. This technique is completely painless and non-invasive and consists in applying an electric current of very low intensity (barely perceptible) at the level of the scalp, using electrodes.

The investigators are conducting a study to test whether transcranial alternating current electrical stimulation could improve the functioning of the inhibition process which is altered in patients. For this, the investigators will measure this process using a task performed on a computer (the Stop Signal Reaction Time Task), as well as brain activity using a method called "electroencephalography", before and after stimulation. For this study, the investigators will include 50 patients and 40 healthy participants to investigate the effect of the stimulation on inhibition.

Registry
clinicaltrials.gov
Start Date
May 3, 2023
End Date
January 15, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • For all participants:
  • Affiliation to a social security scheme or beneficiary of such a scheme.
  • Age over 18 years old.
  • Age less than 75 years old
  • Correct or correctly corrected view (on simple declaration by the patient).
  • Subject having received information on the protocol and having provided informed and written consent to participate.
  • Criteria exclusive to patients:
  • Idiopathic Parkinson's disease according to United Kingdom Parkinson's criteria Brain Bank disease (Hughes et al., 1992).

Exclusion Criteria

  • For all participants:
  • Major cognitive impairment (Moca \< 22) or severe neurocognitive disorder according to DSM-V (Diagnostic and statistical manual of mental disorders -V);
  • Motor difficulties preventing the achievement of the task.
  • Drug or alcohol addiction.
  • Adult subject to legal protection (safeguard of justice, curatorship, guardianship), persons deprived of liberty.
  • Present or past moderate to severe psychiatric pathology (obsessive compulsive, bipolar disorder, schizophrenia, etc.).
  • Potential for pregnancy or confirmed pregnancy. A pregnancy test will be performed on inclusion.for women of childbearing age.
  • Criteria exclusive to patients:
  • Present or past neurological pathology other than Parkinson's disease (accident stroke, head trauma, etc.).
  • Deep brain stimulation treatment.

Outcomes

Primary Outcomes

Difference in cognitive performance measured by the stop signal reaction time (SSRT) compared between real and sham stimulation conditions

Time Frame: 5 months

Secondary Outcomes

  • The difference in the dynamic changes in functional networks during the task between real and sham stimulation.(5 months)
  • The difference in network parameters derived from graph theory between real and sham stimulation.(5 months)
  • The existence of correlations between the changes in network measures between real and sham stimulation mentioned above and the behavioral differences measured between real and sham stimulation.(5 months)

Study Sites (1)

Loading locations...

Similar Trials