Cognitive Stimulation in Elderly Individuals at Risk to Develop Dementia (Allena-Mente). (Allena-Mente)
Primary Purpose
Mild Cognitive Impairment, Healthy Subjects With Family History for Dementia
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Cognitive stimulation
Sanitary education
Sponsored by

About this trial
This is an interventional treatment trial for Mild Cognitive Impairment focused on measuring Mild Cognitive Impairment, Cognitive Stimulation, Aging, Elderly, Randomized Controlled Trial
Eligibility Criteria
Inclusion Criteria:
- Positive diagnosis for mild cognitive impairment (MCI) according to Petersen's criteria;
- Cognitively healthy elderly individuals, having at least one first-degree relative affected by dementia (Alzheimer's Disease, pre-senile and senile dementia, vascular dementia) (NDFAM).
Exclusion Criteria:
- (Major physical illness) Compromission of motor performance of lower and upper limbs
- Medical conditions leading to clinical instability;
- Therapies that reduce cognitive and communicative abilities and consciousness;
- Perceptual disorders (sight, hearing)
- Language disorders
- Education level lower than 3 years
- Psychiatric and behavioral disorders
- Addiction to drugs or alcohol
Sites / Locations
- Golgi Cenci Foundation
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Cognitive stimulation
Sanitary education
Arm Description
Outcomes
Primary Outcome Measures
Long-term change from Baseline in Mini Mental State Examination (MMSE)
Mini Mental State examination (MMSE) is a brief test of mental status and cognitive function, commonly used in clinical research to screen global cognitive functioning.
Secondary Outcome Measures
Change from Baseline in Mini Mental State Examination at 2-weeks after the intervention
MMSE is a brief test of mental status and cognitive function, commonly used in clinical research to screen global cognitive functioning.
Change from Baseline in Montreal Cognitive Assessment (MoCA) at 2-weeks after the intervention
MoCA is a brief cognitive screening tool with a high sensitivity and specificity for detecting MCI in individuals performing in the normal range on the MMSE (avoiding ceiling effect).
Change from Baseline in Corsi test at 2-weeks after the intervention
Corsi test evaluates visual-spatial short-term memory. We used this test to implement non-verbal memory in our neuropsychological test battery
Change from Baseline in Walking While Talking Dual Task at 2-weeks after the intervention
Walking speed measures the ability to perform a dual action task. Single task: participants walk back and forth along an indicated distance of 5 meters with no pausing.
Dual task: participants perform the same movement as in the single task while listing personal names in a loud voice (female names for men and male names for women) The span between time needed to perform the dual and the single task is registered.
Full Information
NCT ID
NCT01793493
First Posted
February 13, 2013
Last Updated
September 11, 2023
Sponsor
Fondazione Golgi Cenci
Collaborators
Alzheimer Federation Italy, Camillo Golgi Geriatric Institute, University of Pavia, Mario Negri Institute for Pharmacological Research
1. Study Identification
Unique Protocol Identification Number
NCT01793493
Brief Title
Cognitive Stimulation in Elderly Individuals at Risk to Develop Dementia (Allena-Mente).
Acronym
Allena-Mente
Official Title
Effects of Cognitive Stimulation in Elderly Individuals at Risk to Develop Dementia: a Randomized Controlled Trial (Allena-Mente).
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
March 2011 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
June 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fondazione Golgi Cenci
Collaborators
Alzheimer Federation Italy, Camillo Golgi Geriatric Institute, University of Pavia, Mario Negri Institute for Pharmacological Research
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The Allena-Mente study is a randomized, controlled, single-blind trial assessing the efficacy of cognitive stimulation (CS) compared to an active control group, participating to sanitary education lessons (AC). This non-pharmacological intervention is delivered to Mild Cognitive Impairment (MCI) and cognitively healthy individuals with first-degree relative with dementia (NDFAM).
Detailed Description
The experimental protocol was set up with a pilot study on healthy elderly individuals. Data from this pilot study will be excluded from the statistical analysis.
Sample size: a priori power analysis was performed to evaluate the sample size required for the study. MCI and NDFAM were considered separately for sample size calculation. For power calculation a two-tailed test was used and a significance level (α) and test power (1-β) were set at 0.05 and 0.8/0.9, respectively.
Randomization: The individuals belonging to MCI and NDFAM subgroup were randomly assigned to CS or AC group. The randomization was performed by a statistician blind to participants characteristics using the Random Allocation Software. Allocation ratio was set at 1:1, stratification was performed for birth cohort (≤1937 and ≥1938), education level (years of education ≤5 years and >5 years).
Participants provided written informed consent before study participation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild Cognitive Impairment, Healthy Subjects With Family History for Dementia
Keywords
Mild Cognitive Impairment, Cognitive Stimulation, Aging, Elderly, Randomized Controlled Trial
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
121 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Cognitive stimulation
Arm Type
Experimental
Arm Title
Sanitary education
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Cognitive stimulation
Intervention Description
Participants are pooled in small groups (6-8 individuals). Each group participates to ten twice weekly meetings. Each CS session is run by one trained operator. One observer participates to the sessions to guarantee homogeneity between different operators. Exercises are structured with an increasing cognitive complexity and are tailored to the characteristics of the group.
Meetings (each lasting about 2 hours) have a common structure:
body awakening (10 minutes)
cognitive stimulation (1 hour and a half) scheduled as follow:
temporospatial orientation
attentional abilities
one of the following cognitive areas: language, executive functions, verbal and visual memory (encoding, consolidation, retrieval)
Intervention Type
Other
Intervention Name(s)
Sanitary education
Intervention Description
Participants attend two weekly meetings (for a total of 3 hours) focused on lifestyle education and brain functioning.
Primary Outcome Measure Information:
Title
Long-term change from Baseline in Mini Mental State Examination (MMSE)
Description
Mini Mental State examination (MMSE) is a brief test of mental status and cognitive function, commonly used in clinical research to screen global cognitive functioning.
Time Frame
baseline and up to 4 years
Secondary Outcome Measure Information:
Title
Change from Baseline in Mini Mental State Examination at 2-weeks after the intervention
Description
MMSE is a brief test of mental status and cognitive function, commonly used in clinical research to screen global cognitive functioning.
Time Frame
baseline, two-weeks after the intervention
Title
Change from Baseline in Montreal Cognitive Assessment (MoCA) at 2-weeks after the intervention
Description
MoCA is a brief cognitive screening tool with a high sensitivity and specificity for detecting MCI in individuals performing in the normal range on the MMSE (avoiding ceiling effect).
Time Frame
baseline, two-weeks after the intervention
Title
Change from Baseline in Corsi test at 2-weeks after the intervention
Description
Corsi test evaluates visual-spatial short-term memory. We used this test to implement non-verbal memory in our neuropsychological test battery
Time Frame
baseline, two-weeks after the intervention
Title
Change from Baseline in Walking While Talking Dual Task at 2-weeks after the intervention
Description
Walking speed measures the ability to perform a dual action task. Single task: participants walk back and forth along an indicated distance of 5 meters with no pausing.
Dual task: participants perform the same movement as in the single task while listing personal names in a loud voice (female names for men and male names for women) The span between time needed to perform the dual and the single task is registered.
Time Frame
baseline, two-weeks after the intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
70 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Positive diagnosis for mild cognitive impairment (MCI) according to Petersen's criteria;
Cognitively healthy elderly individuals, having at least one first-degree relative affected by dementia (Alzheimer's Disease, pre-senile and senile dementia, vascular dementia) (NDFAM).
Exclusion Criteria:
(Major physical illness) Compromission of motor performance of lower and upper limbs
Medical conditions leading to clinical instability;
Therapies that reduce cognitive and communicative abilities and consciousness;
Perceptual disorders (sight, hearing)
Language disorders
Education level lower than 3 years
Psychiatric and behavioral disorders
Addiction to drugs or alcohol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antonio Guaita, MD
Organizational Affiliation
GolgiCenci Foundation
Official's Role
Study Director
Facility Information:
Facility Name
Golgi Cenci Foundation
City
Abbiategrasso
State/Province
Milan
ZIP/Postal Code
20081
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
25187003
Citation
Polito L, Abbondanza S, Vaccaro R, Valle E, Davin A, Degrate A, Villani S, Guaita A. Cognitive stimulation in cognitively impaired individuals and cognitively healthy individuals with a family history of dementia: short-term results from the "Allena-Mente" randomized controlled trial. Int J Geriatr Psychiatry. 2015 Jun;30(6):631-8. doi: 10.1002/gps.4194. Epub 2014 Sep 3.
Results Reference
background
Links:
URL
http://www.golgicenci.it
Description
official web site of the organization responsible for the study
URL
http://www.alzheimer.it
Description
official website of the caregivers organization, partner in the sponsorship of the research
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Cognitive Stimulation in Elderly Individuals at Risk to Develop Dementia (Allena-Mente).
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