Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:11 AM
Ignite Modification Date:
2025-12-25 @ 4:11 AM
NCT ID:
NCT07068620
Eligibility Criteria:
Inclusion Criteria:
* Patients included or previously included in the SHIVA cohort
* Basic computer skills (ability to open a browser, use a mouse and keyboard)
* Access to a personal computer with an internet connection
* Independent in Activities of Daily Living (ADL) with a score ≥ 5/6, and in Instrumental Activities of Daily Living (IADL) with a score ≥ 4/8
* Informed and written consent signed by the participant and the investigating physician for this study
Exclusion Criteria:
* Motor impairments preventing the use of a keyboard and mouse (e.g., motor issues related to severe hand osteoarthritis)
* Depressive symptoms indicated by a score of 2 to 4 on the mini Geriatric Depression Scale (mini GDS), which includes 4 items
* Age-related macular degeneration (AMD)
* Untreated glaucoma
* Untreated psychiatric conditions that interfere with cognitive assessments
* Diagnosed attention deficit disorder with or without hyperactivity or patients who could not complete all cognitive tests required in the SHIVA cohort
* Systemic diseases that cause cognitive changes, such as obesity and metabolic disorders
* History of epilepsy or seizures
* Scalp sensitivity or skin lesions (dermatitis, wounds, etc.)
Contraindications for the use of electrical stimulation:
* Surgical clips, metal sutures, staples, stents
* Osteosynthesis material in the head or neck
* Pacemaker
* Implanted hearing aid
* Ocular foreign bodies, shrapnel, bullets
* Metalworker
* Pacemaker or neurostimulator
* Heart valve or endovascular material
* Ventricular shunt valve
* Recent exposure (\< 6 months) to brain stimulation (tDCS, TMS, etc.)
* Ongoing participation in a clinical trial or cognitive training program
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07068620
Study Brief:
Protocol Section:
NCT07068620