Five Lives MED to Improve Cognitive Function in Mild Cognitive Impairment
Recruiting
N/AInterventional Study
Mild Cognitive Impairment
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
50 and older
Sex
Any
Study type
Interventional
Purpose
Basic Science
Participants needed
170 (estimated)
Sponsor
SharpTx · Industry
Who this trial is looking for
This trial is looking for adults aged 50 and older with mild cognitive impairment (MCI). Participants will use the Five Lives MED app at home for 12 weeks and complete cognitive tests and questionnaires.
Are You a Good Fit for This Trial?
You may be able to join if
I have been diagnosed with mild cognitive impairment.
I am 50 years old or older.
I can give informed consent to participate.
I can read and understand English or French.
I have access to a compatible mobile device with internet.
You may not be able to join if
I have been diagnosed with dementia.
I have severe visual impairment.
I am currently undergoing another cognitive program.
I am participating in another study that may affect this study.
I have a physical impairment that makes using a mobile device impossible.
I do not have access to an informant.
I am under guardianship.
I am unwilling or unable to engage with the study.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The goal of this randomized controlled trial is to determine whether the digital health app Five Lives MED can improve cognitive function in people with mild cognitive impairment (MCI). The main question it aims to answer is:
Can 12 weeks of using Five Lives MED improve global cognitive function in people diagnosed with MCI?
Researchers will compare with a control group who receives a leaflet wi…
The goal of this randomized controlled trial is to determine whether the digital health app Five Lives MED can improve cognitive function in people with mild cognitive impairment (MCI). The main question it aims to answer is:
Can 12 weeks of using Five Lives MED improve global cognitive function in people diagnosed with MCI?
Researchers will compare with a control group who receives a leaflet with standard health information.
Participants in the intervention group will be asked to use the Five Lives MED app 3 times per week at home for 12 weeks.
All participants, in both groups, will undergo cognitive testing and will complete questionnaires at baseline and exit.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Diagnosis of Mild Cognitive Impairment (also known as mild cognitive disorder \[ICD-10-CM; G31.84\] or mild neurocognitive disorder (DSM-5)
* Age ≥ 50
* Participant or informant is willing and able to give informed consent for participation in the study
* Ability to read and u…
Inclusion Criteria:
* Diagnosis of Mild Cognitive Impairment (also known as mild cognitive disorder \[ICD-10-CM; G31.84\] or mild neurocognitive disorder (DSM-5)
* Age ≥ 50
* Participant or informant is willing and able to give informed consent for participation in the study
* Ability to read and understand English (UK) or French (France)
* Access to a mobile phone (Apple iOS 12.4 or above or Android 6.0 (Marshmallow) or above) or iPad (Apple iOS 12.4 or above only) with internet connection (mobile or WiFi).
Exclusion Criteria:
* Diagnosis of dementia or evidence of functional impairment inconsistent with MCI
* Severe visual impairment
* Currently undergoing any other cognitive remediation programme
* Currently taking part in any other investigational study that in the opinion of the investigator may impact the data integrity of the current study
* Physical impairment that makes using a mobile device impossible
* Lack of access to an informant
* Participant under guardianship
* Unwilling or unable to tolerate or engage with study procedures
* Physical impairment that makes standing/walking unassisted impossible.
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