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 @ 1:46 AM
Ignite Modification Date:
2025-12-25 @ 1:46 AM
NCT ID:
NCT04658394
Eligibility Criteria:
Inclusion Criteria:
* Having a formal diagnosis of a neurocognitive disorder according to Diagnostic and Statistical Manual of Mental Disorders, fifth edition \[DSM-5\] criteria (participants diagnosis will be confirm in their health records at the institution).
* Having delivered the informed consent form, duly completed and signed, after prior information.
* Being able to communicate and understand.
* Possibility of gathering information about the participant's life history through family members or usual caregivers, using the socio-family questionnaire designed for that purpose.
* Being 65 years of age or older.
* Being a native Portuguese speaker.
* Regularly attending an institution that provides social care and support services for older adults (including people living in long-term care centres, people attending day and social centres and people receiving home support services).
Exclusion Criteria:
* Suffering from an acute or severe illness that prevent participation in the intervention sessions.
* Severe sensory and physical limitations that prevent participation.
* Low level of consciousness and minimal attention span.
* Presence of severe neuropsychiatric symptoms, such as agitation, psychosis, severe depressive and anxiety symptoms, apathy, or presence of uncontrolled delirium that prevent participation in the sessions.
* Traumatic life history or marked by adverse events that discourage participation in RT sessions; history of adverse reactions during RT sessions or similar activities.
* Have a serious or total functional dependence (assessed through the Barthel index).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
65 Years
Study:
NCT04658394
Study Brief:
Protocol Section:
NCT04658394