Skip to content

PsyDoMa : Non-drug Approaches at Home for Alzheimer's Patients With Psycho-behavioural Disorders

PsyDoMa :Non-drug Approaches at Home for Alzheimer's Patients With Psycho-behavioural Disorders and Psycho-education for the Caregivers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04573829
Acronym
PSYDOMA
Enrollment
40
Registered
2020-10-05
Start date
2021-01-14
Completion date
2022-09-19
Last updated
2022-10-07

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

Conditions

Behavioral Disorder

Brief summary

Recruitment is carried out directly at the geriatric unit of the CIMIEZ University Hospital Center by geriatric doctors during day consultation or in short stay unit. The doctor wil select carer -patient couples more likely to take part in the study. The investigator will give them an informative leaflet and they will have to sign the consent form. A diagnosis is made by the investigator. The patient will first have to undergo a neurocognitive assessment carried out at the Cimiez Hospital (test for the evaluation of a cognitive deficit) by a psychologist. The non-drug approaches presented will be carried out directly at the participant's home with the help of the carer for therapeutic purposes. The therapeutic objectives and the choice of approaches are specified within the Personalised Accompaniment Project (PAP). The carer, if he or she wishes, participates in the sessions in order to reproduce the behaviours implemented by the psychologist. Different workshops will be offered : Cooking, Art Therapy, Games, Multi-sensory, Soft Gymnastic, Relaxation, Music and Reminisence. Patients will received three visits per week during six months. The carer will receive one visit per week for six months.

Interventions

PROCEDUREHome visit

Psychologist come once a week for the carer and three times a week for the patient

Sponsors

Fondation Mederic Alzheimer
CollaboratorOTHER
Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

For Patients * Men or women over 65 years old showing signs of cognitive decline * Living at home with specific needs ( meals, etc.) and the regular presence of a carer, * Living in Nice * Diagnosed with Alzheimer or dementia * Presence of at least one behavioural disorder * Person who agreed and signed the informed consent or his/her guardian For Carers * Carer of the patient who meets the inclusion criteria: spouse, children, siblings or other family members at home or a professional carer. * Person involved during the motivational interviewing session regarding the psychoeducational program. * Person who agreed and signed the informed consent.

Exclusion criteria

For patients : * Elderly person presenting no NINCDS- ADRDA criteria, * Presence of sensory deficit (hearing or vision) * Person unable to communicate, * No regular presence of a home carer, waiting for a place in a nursing home * Aging psychiatric pathologies, * Elderly person attending a day-care centre For carers : * carer absent or not present enough, * Elderly person with undiagnosed behavioural disorders * Drug treatment that can interfere with assessments (psychotropic drugs, neuroleptics, etc.).

Design outcomes

Primary

MeasureTime frame
Ratio of personalised care projects completedat the end of 6 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026