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Improving cognitive performance in MS by transcranial alternating current brain stimulation (tACS): a pilot study

Improving cognitive performance in MS by transcranial alternating current brain stimulation (tACS): a pilot study - Cognitive function in MS after tACS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON49662
Enrollment
45
Registered
2017-06-19
Start date
2017-11-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

cognitive impairment MS nervous system

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: MS Patients: Diagnosis of MS according to the MacDonald criteria Age: 30 - 60 years Cognitive impairment (CI): CI patients will have decreased values (1.5 standard deviations below the normative control values or below cut-off value for deviation) on at least 2 tests from NPE battery. Signed written informed consent and right handedness. Healthy participants: Age: 30 - 60 years Signed written informed consent and right handedness.

Exclusion criteria

Exclusion criteria: 1. History of psychiatric or neurological illness other than MS for MS patients or History of psychiatric or neurological illness for healthy participants 2. Metal implants (e.g., pacemaker, heart valves, vascular clips, eye-implants, copper containing intra-uterine devices, non-removable piercing, cerebral implants) 3. Any risk of having metal particles in the eyes 4. Tattoos containing iron oxide (often found in red pigments) 5. (Suspected) Pregnancy or breast feeding 6. Claustrophobia 7. Alcohol or drug abuse 8. Excessive intake of coffee (>5 units per day) or alcohol (>2 units per day); 9. Recent use of alcohol (2 days before the EEG and/or fMRI measurement). 10. Recent use (within one week) of cannabis, benzodiazepine, baclofen or any other nonprescription psychopharmaca; 11. Refusal to be informed of structural brain abnormalities that could be detected during the experiment 12. Diagnosis of epilepsy, Parkinson*s disease, Myasthenia Gravis, epilepsy and dementia. 13. Severe scalp skin lesions 14. Color blindness

Design outcomes

Primary

MeasureTime frame
The changes in EEG coherence and in speed of information processing in patients with MS using tACS. EEG coherence will be estimated between frontal and parietal regions from RS EEG recordings. The information processing speed will be measured using the Vienna Reaction Time Task (VRTT).

Secondary

MeasureTime frame
n.a.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)