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Sensory Support Care for Elderly Patients Suffering From Alzheimer'S-type Neurodegenerative Disease

Evaluation of the Impact of Care Based on Sensory Support for Elderly Patients Suffering From Alzheimer'S-type Neurodegenerative Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01819714
Acronym
SensiCare
Enrollment
31
Registered
2013-03-28
Start date
2013-06-30
Completion date
2015-02-28
Last updated
2015-04-29

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

Conditions

Alzheimer Disease

Keywords

Snoezelen, Multi-sensorial care session, Alzheimer's-type neurodegenerative disease, Dementia

Brief summary

The main objective of this study is to evaluate the effect of 3 months of Snoezelen-type multi-sensory care sessions on NeuroPsychiatric Inventory Questionnaire (NPI-Q) scores for patients with Alzheimer's-type neurodegenerative disease.

Detailed description

The secondary objectives of this study are to study the following elements in relationship to the implementation of a Snoezelen-type multi-sensory care strategy for patients with Alzheimer's-type neurodegenerative disease: A. to evaluate the effects on NPI-Q scores at 1 month, 6 months and 12 months . B. evaluate the effects on quality of life (questionnaire QOL-AD) at 0 and 12 months. C. assess changes in the aggressive behavior subsection of the Cohen-Mansfield Agitation Inventory (CMAI) questionnaire over 0, 1, 3, 6 and 12 months. D. assess changes in drug consumption (anxiolytics, antidepressants, hypnotics, neuroleptics)over the study period

Interventions

OTHERMulti-sensory supportive care

The Serre-Cavalier center will implement Snoezelen-type multisensory care sessions for included patients; these care sessions correspond with the patients' daily hygiene/toilette care. The impact of this multisensory strategy will be evaluated using a before-after design.

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* The patient's legal representative must have given his/her informed and signed consent (or the patient if he/she is judged competent) * The patient must be insured or beneficiary of a health insurance plan * Alzheimer's-type neurodegenerative pathology * The patient has been living in the participating center for \> 2 months

Exclusion criteria

* The patient's legal representative refuses to sign the consent (or the patient if he/she is judged competent) * It is impossible to correctly inform the patient's legal representative * The patient has already has Snoezelen-therapy

Design outcomes

Primary

MeasureTime frame
Change from baseline in NPI-Q scores3 months

Secondary

MeasureTime frame
Change from baseline in NPI-Q scores1 month
Change from baseline in the Quality-of-life-Alzheimer's Disease questionnaire (QOL-AD)12 months
Change from baseline in the aggressive behavior subsection of the Cohen-Mansfield Agitation Inventory (CMAI) questionnaire1 month
Change in drug consumption from baseline1 month

Countries

France

Outcome results

None listed

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