Effect of Individual Cognitive Stimulation on Memory and Executive Function in Older Adults With Alzheimer's Disease
- Conditions
- Neurocognitive DisordersCognitive DeclineDementiaCognitive ImpairmentCognitive Dysfunction
- Interventions
- Behavioral: Cognitive stimulation
- Registration Number
- NCT05433493
- Lead Sponsor
- Rsocialform - Geriatria, Lda
- Brief Summary
This multicentre study, with a randomised controlled repeated measures experimental design, will be conducted in several Portuguese institutions, which provide care and supportive services for older adults diagnosed with mild or moderate Alzheimer's disease (AD), with an aim to assess the effect of individual cognitive stimulation (CS) on memory and executive functioning. Participants in the intervention group will attend 24 individual CS sessions, twice weekly for 12 weeks. Participants in the control group will complete their usual routines without any activity restrictions.
- Detailed Description
Neurocognitive disorders (NCD) currently affect around 55 million people worldwide and expected to increase to 78 million by 2030 and 139 million by 2050, with Alzheimer's disease (AD) potentially accounting for 60-70% of dementia cases. Dementia is a syndrome, generally chronic or progressive in nature, that causes deterioration of cognitive function, particularly memory and executive functions, beyond what is expected in normal aging. However, there is evidence that in the early stages of NCD, people can learn and improve their cognitive functions through interventions such as CS. CS is a psychosocial intervention and a non-pharmacological therapy recommended by international practice guidelines for people with mild-to-moderate stage AD. However, it is also important to investigate whether NCD generates new skills or only preserves acquired skills, given that AD manifests initially and notably with deficits in memory and learning, sometimes accompanied by deficits in executive functions. Testing the effectiveness of CS by recruiting a representative sample from several Portuguese districts and using a CS programme with detailed and comprehendible content, may elicit relevant evidence in clinical practice, contribute to the development of social development programs and initiatives to ensure social protection and inclusion, promote recurrent therapeutic interventions in Portuguese institutions with provide care and supporting services for older adults with dementia, and strengthen research on non-pharmacological therapies. Thus, this multicentre, randomised controlled study is essential to analyse the effects of the individual CS on global cognitive function and specific cognitive domains (e.g., executive functioning, memory) in older adults with mild or moderate AD.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 142
- Age 65 or over.
- Receive care and support services for older adults for at least three months.
- Alzheimer's disease, according to the criteria of the Diagnostic and Statistical Manual of Mental Disorders, 5th edition.
- Ability to communicate and understand.
- Native speakers of Portuguese.
- To have given informed consent for the project, duly completed and signed, after previous information.
- Total scores between 10 and 24 points on the Mini Mental State Examination.
- Cannot read and write.
- Severe sensory and physical limitations and/or an acute or serious illness preventing participation in the CS sessions.
- Evidence of aggressive and disruptive behaviour, as indicated by the reference technicians of the institution to which the participant is linked.
- Consumption of psychoactive substances, taking neuroleptics and/or antipsychotics in the last two months.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention group Cognitive stimulation Participants who meet the inclusion criteria will be randomly assigned to the intervention group receiving individual CS or to the control group receiving treatment as usual (participating in the activities previously established in their individual intervention plan). Participants in the intervention group will participate in two individual CS sessions per week for 12 weeks in addition to their treatment as usual. The sessions will include the same protocol in every participant site.
- Primary Outcome Measures
Name Time Method Memory function evaluated through Free and Cued Selective Reminding Test (FCSRT) baseline FCSRT is a verbal learning and memory test that allows prompting the encoding and retrieval conditions by using semantic cues on learning and recall trials. It is composed of 16 semantically categorised, unrelated items/words.
Cognitive functioning assessed through Mini-Mental State Examination (MMSE) baseline Cognitive functioning assessed by the Mini-Mental State Examination (MMSE), a gold standard screening tool for assessing global cognitive function. Scores range from 0 to 30, with higher scores indicating better cognitive functioning.
Cognitive functioning assessed through Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-COG) baseline Evaluates the severity of cognitive deficits in AD in the following domains: memory, orientation, language, praxis and constructive capacity. The total score in the Portuguese version of ADAS-Cog is composed of 11 subtests in the cognitive part and varies between 0 (better performance) and 68 points (worse performance), i.e., higher scores equals better performance.
Memory function evaluated through Memory Alteration Test (MAT) baseline The MAT is used to assess memory function. It is an easy and quick instrument that assesses five memory domains: temporal orientation, encoding, semantic memory, free recall, and cued recall. Total scores range from 0 to 50, with higher scores indicating better memory. It has good psychometric properties and is highly sensitive to mild cognitive decline.
Change in memory function evaluated through Memory Alteration Test (MAT) 12 weeks after end of intervention The MAT is used to assess memory function. It is an easy and quick instrument that assesses five memory domains: temporal orientation, encoding, semantic memory, free recall, and cued recall. Total scores range from 0 to 50, with higher scores indicating better memory. It has good psychometric properties and is highly sensitive to mild cognitive decline.
Change in memory function evaluated through Free and Cued Selective Reminding Test (FCSRT) 12 weeks after end of intervention FCSRT is a verbal learning and memory test that allows prompting the encoding and retrieval conditions by using semantic cues on learning and recall trials. It is composed of 16 semantically categorised, unrelated items/words.
Change in cognitive functioning assessed through Mini-Mental State Examination (MMSE) 12 weeks after end of intervention Change in cognitive functioning evaluated by the Mini-Mental State Examination (MMSE), a gold standard screening tool for assessing global cognitive function.
Scores range from 0 to 30, with higher scores indicating better cognitive functioning.Executive functions assessed through Frontal Assessment Battery (FAB) baseline FAB assesses executive functions such as abstract thinking, mental flexibility, motor programming, interference sensibility, inhibitory control and environmental independence. Scores range between 0 - 18 points with higher scores indicating better cognitive function.
Change in executive functions assessed through Trail Making Test (TMT) 12 weeks after end of intervention TMT is one of the most widely used instruments in clinical and experimental neuropsychology. It is very sensitive to identify cognitive impairments, measuring simple motor and spatial skills, basic sequencing skills, mental flexibility, selective attention, visuo-perceptual skills, motor speed, and executive functions. Higher scores indicate greater impairment.
Change in cognitive functioning assessed through Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-COG) 12 weeks after end of intervention Evaluates the severity of cognitive deficits in AD in the following domains: memory, orientation, language, praxis and constructive capacity. The total score in the Portuguese version of ADAS-Cog is composed of 11 subtests in the cognitive part and varies between 0 (better performance) and 68 points (worse performance), i.e., higher scores equals better performance.
Change in executive functions assessed through Frontal Assessment Battery (FAB) 12 weeks after end of intervention FAB assesses executive functions such as abstract thinking, mental flexibility, motor programming, interference sensibility, inhibitory control and environmental independence. Scores range between 0 - 18 points with higher scores indicating better cognitive function.
Executive functions assessed through Trail Making Test (TMT) baseline TMT is one of the most widely used instruments in clinical and experimental neuropsychology. It is very sensitive to identify cognitive impairments, measuring simple motor and spatial skills, basic sequencing skills, mental flexibility, selective attention, visuo-perceptual skills, motor speed, and executive functions. Higher scores indicate greater impairment.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (14)
Cediara - Associação de Solidariedade Social de Ribeira de Fráguas
🇵🇹Aveiro, Portugal
Centro Social e Cultural S. Pedro de Bairro
🇵🇹Braga, Portugal
Rsocialform - Geriatria, Lda
🇵🇹Mealhada, Aveiro, Portugal
Centro Social Vale do Homem - Casa da Alegria
🇵🇹Braga, Portugal
Santa Casa da Misericórdia de Castro Marim
🇵🇹Faro, Portugal
Associação de Socorros da Freguesia de Turcifal
🇵🇹Lisboa, Portugal
Centro de Apoio Social de Oeiras - IASFA
🇵🇹Lisboa, Portugal
Associação de Apoio Social de Perafita
🇵🇹Porto, Portugal
Santa Casa da Misericórdia de Coruche
🇵🇹Santarém, Portugal
Fundação João Bento Raimundo
🇵🇹Guarda, Portugal
Santa Casa da Misericórdia de Alcobaça
🇵🇹Leiria, Portugal
Santa Casa da Misericórdia de Ponte de Lima
🇵🇹Viana Do Castelo, Portugal
Inválidos do Comércio
🇵🇹Lisboa, Portugal
Santa Casa da Misericórdia da Horta
🇵🇹Açores, Portugal