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NCT Number: NCT05709210

Pilot Study on the Feasibility of Using Smartphone Data as a Diagnostic Marker for Alzheimer's Disease

This study will compare smartphone usage data between three groups of patients diagnosed with either a memory complaint, mild cognitive decline, or Alzheimer's disease.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

About this study

Alzheimer's disease (AD) is the leading cause of dementia in the world. The first cognitive function affected is memory and then other cognitive systems are affected leading to a progressive loss of autonomy of the patient. Currently, the diagnosis of AD is made at too late a stage. Patients with memory complaints or mild cognitive decline (MCI) are particularly at risk of developing AD.

However, there is no clinical or paraclinical evidence to predict precisely this risk of progression to AD. Investigator's hypothesis is that there is an association between the evolution of smartphone use and the conversion of cognitive status to AD.

The purpose of this pilot study is to identify existing differences between smartphone use data of patients with a memory complaint or of patients MCI or with an AD. It is a study of 90 patients (30 patients with memory complaint, 30 with MCI and 30 with AD) with a collection of smartphone usage data during three months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient consulting in routine care in one of the CMRR
  • No sensory impairment that may compromise smartphone use

Exclusion criteria

  • Inability to perform MMSE or MMSE < 20 ;
  • Other neurodegenerative condition (Parkinson's disease, Lewy body disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis)
  • Severe anxiety or depressive disorder HADS score ≥ 17
  • Terminal phase of a severe disease
  • Evidence of a lesion on MRI that may be involved in cognitive impairment

Treatment and study plan

Recording of smartphone usage data

Other

Recording of smartphone usage data

Primary outcomes

  1. Comparison of a mathematical combination

    Time frame: Up to three months

    The comparison of a mathematical combination of the different parameters collected during the three months of smartphone data recording

Sponsors and collaborators

Lead sponsor

Poitiers University Hospital

Other

Collaborators

  • University of Poitiers

Registry information

Acronym: IMASMART

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Feb 2, 2023
Registry last updated
Jul 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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