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Efficacy of the Memory Motivation (MEMO) Web Application Training

Efficacy of the Memory Motivation (MEMO) Web Application for Cognitive and Behavioral Training in Patients With Neurocognitive Disorders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04142801
Acronym
MeMo
Enrollment
49
Registered
2019-10-29
Start date
2017-05-05
Completion date
2019-08-10
Last updated
2019-10-29

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

Conditions

Neurocognitive Disorders

Keywords

Cognition, motivation, technology, non pharmacological intervention

Brief summary

Memory, attentional, and behavioural symptoms are the clinical hallmarks of Neurocognitive disorders (NCD) such as Alzheimer's disease and related disorders. The World Health Organisation (WHO) guidelines for risk reduction of cognitive decline and dementia indicate that Cognitive training may be offered to older adults with normal cognition and with mild cognitive impairment to reduce the risk of cognitive decline and/or dementia. The use of Information and Communication Technologies (ICT) in the health domain is progressively expanding. The Alzheimer Innovation Association have developed MeMo (Memory Motivation) a free web application that can be used at home by patients. The objective of the present study was to assess the effectiveness of employing the MeMo platform on cognitive performance in patients suffering from NCD.

Detailed description

The objective of this study is to evaluate the effectiveness of the MeMo cognitive training exercise platform in patients suffering from neurocognitive disorders. These exercises ,have been developed by the association Innovation Alzheimer and the CoBTeK research team, located with the Nice memory Center at the Institut Claude Pompidou. MeMo can be used freely at home by patients. More specifically, it is a randomized controlled study that aims to compare the evolution of activities cognition and behavior between patients not using these exercises, and patients using these exercises for 12 weeks, 4 sessions per week.

Interventions

DEVICEMeMo web application

The patient betwenn 2 consultation could use the application MeMo. MeMo is a web application that can thus be used on any web browser (computer or tablet). On tablet, the application can be installed on home screen to look like a native app, and used offline.

OTHERControl group

the patient have the classical follow up at the memory center (consultation)

Sponsors

Alzheimer's Association
CollaboratorOTHER
Centre Hospitalier Universitaire de Nice
CollaboratorOTHER
Université de Nice Sophia Antipolis
CollaboratorOTHER
Innovation Alzheimer
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

Randomization for the allocation of the patient in each group

Intervention model description

regular use of a web application at home to train cognition and behavior

Eligibility

Sex/Gender
ALL
Age
60 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Outpatient consulting the Memory center * older than 60 years old * Mini Mental State examination score (MMSE) between 16 and 28 / 30 * met the DSM 5 diagnoses of mild neurocognitive disorders (mild NCD) or major neurocognitive disorders (Major NCD).

Exclusion criteria

* Patients not able to read and write French * presence of a hearing or major visual impairment * a history of premorbid mental retardation * had already used the MeMo application * were presently involved in structured memory training activities.

Design outcomes

Primary

MeasureTime frameDescription
Change is being assessed with the Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE)Base line, Week 12To score the IQCODE, add up the score for each question and divide by the number of questions. For the long IQCODE, divide by 26.

Secondary

MeasureTime frameDescription
Change in attention is is being assessed with the DSSTBase line, Week 12Digit Symbol Substitution Test (attentional task)
Change in frontal functioning is being assessed with the FABBase line, Week 12the Frontal Assessment Battery: Score 0 (healthy) - 18 (pathology)
Change in behavior is being assessed with the NPIBase line, Week 12Neuropsychiatric Inventory score 0 (healthy) - 134 (pathology)
IA-CBase line, Week 12Change in motivation is being assessed with theApathy inventory, clinician version score 0 (healthy)- 12 (pathology)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026