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NCT05340218

Short-term Automated Longitudinal Analysis of Speech and Language in Cognitive Impairment

Completed NA Last updated 25 March 2026
What this trial tests

NA trial testing Speech analysis in Mild Cognitive Impairment in 196 participants. Completed in 22 March 2022.

Timeline
1 January 2019
Primary endpoint
22 March 2022
22 March 2022

Quick facts

Lead sponsorAccexible
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designparallel
Maskingnone
Primary purposediagnostic
Enrollment196
Start date1 January 2019
Primary completion22 March 2022
Estimated completion22 March 2022
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Accexible — full company profile →

Who can join

Adults 55 to 90, any sex, with Mild Cognitive Impairment or Dementia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Validate speech analysis AI models: * To contrast the accuracy of acceXible's platform as a screening tool in the detection of people with cognitive impairment and mild dementia. * To evaluate the correlation between automatically analyzed linguistic variables and a combination of standard measures of cognition. * To assess short-term variability in language ability among older adults, and to assess which aspects of language vary during the study period.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Speech analysis

Trials testing the same drug.

Other recruiting trials for Mild Cognitive Impairment

Currently open trials in the same condition.

Other Accexible trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05340218.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing