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:
2025-12-24 @ 5:37 PM
Ignite Modification Date:
2025-12-24 @ 5:37 PM
NCT ID:
NCT05262868
Eligibility Criteria:
Inclusion Criteria:
* Informed consent as documented by their and their proxy's signature (Appendix Informed Consent Form)
* Consent for MRI
* Age ≥ 65 years
* Clinical dementia Rating Scale (CDR) ≥ 1
* NPI-Q Σ (\*Anxiety + \* Apathy/Indifference + \* Dysphoria/Depression) ≥ 3
* Cornell Scale for Depression in Dementia (CSDD) ≥ 10
Exclusion Criteria:
* History of schizophrenia, bipolar disorder, schizoaffective disorder
* History of macroscopic stroke.
* Unstable somatic pathologies
* Insufficient collaboration for the rTMS procedure
* Drug freeness or drug adjustment as clinically required is not an exclusion criterion.
* The proxy refuses to give consent in case of lack of capacity, or in any case where the participant expresses a wish not to participate/continue in the study.
* Any contraindications to performing an MRI (cf CRF) and rTMS (aneurysm clips or coils, stents in the neck or brain, deep brain stimulators, electrodes to monitor brain activity, metal implants in the ears and eyes, facial tattoos with metallic or magnetically sensitive ink) procedure
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
65 Years
Study:
NCT05262868
Study Brief:
Protocol Section:
NCT05262868