Effectiveness of a Cognitive Training Program (UMAM Method) in Elderly People Without Dementia
NCT ID: NCT04245579
Last Updated: 2020-01-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
199 participants
INTERVENTIONAL
2013-10-31
2015-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Experimental Group
The experimental group carried out a 30-session multi-factorial group memory training program (UMAM method), with a frequency of three weekly sessions of 90 minutes each. The training program consists of four modules: 1- Stimulation of cognitive processes; learning and practicing internal memory strategies and solving everyday forgetfulness; 2- Instruction in basic concepts about memory; 3- Intervention on daily living and forgetting experiences, using internal and external strategies to solve everyday memory failures; 4- Metacognition or metamemory: the subjects were to reflect about their cognitive failures by analyzing the causes and variables of those failures.
In addition, the experimental group followed the standard activities in which all users attending the Center are involved (planned interviews, dialogue-conferences, general health recommendations, etc.).
Multifactorial Memory Training Program (UMAM method)
Control Group
The Control Group followed the standard activities in which all users attending the Center are involved (planned interviews, dialogue-conferences, general health recommendations, etc.).
No interventions assigned to this group
Interventions
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Multifactorial Memory Training Program (UMAM method)
Eligibility Criteria
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Inclusion Criteria
* Having a global cognitive performance \> 23 in the Mini Mental State Examination Test.
* Having no history of neurological or serious psychiatric disorders (severe psycho-affective disorders and psychosis or other psychiatric disorders like alcoholism).
Exclusion Criteria
* Chronic use of neuroleptics.
* Chronic use of anticonvulsants.
* Having hearing or vision impairments that would preclude testing.
* Magnetic Resonance Imaging (MRI) contraindications.
60 Years
ALL
Yes
Sponsors
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Universidad Complutense de Madrid
OTHER
Hospital San Carlos, Madrid
OTHER
Centro de Tecnología Biomédica, Madrid
UNKNOWN
Madrid Salud
OTHER
Responsible Party
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Locations
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Centro de Prevención del Deterioro Cognitivo
Madrid, , Spain
Countries
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References
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Montejo Carrasco P, Montenegro-Pena M, Prada Crespo D, Rodriguez Rojo I, Barabash Bustelo A, Montejo Rubio B, Marcos Dolado A, Maestu Unturbe F, Delgado Losada ML. APOE genotype, hippocampal volume, and cognitive reserve predict improvement by cognitive training in older adults without dementia: a randomized controlled trial. Cogn Process. 2024 Nov;25(4):673-689. doi: 10.1007/s10339-024-01202-3. Epub 2024 Jun 19.
Other Identifiers
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15/382-E_BS
Identifier Type: -
Identifier Source: org_study_id
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