Validating Studies to Assess the Diagnostic Accuracy of a Software Application for Detection and Monitoring of Attentional Deficits in Delirium

NCT02590796 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 907

Last updated 2018-05-24

No results posted yet for this study

Summary

The study has two phases: Phase B and Phase C. The purpose of the Phase B study is to determine the performance (sensitivity and specificity) of a smartphone application (DelApp) to identify delirium in the whole inpatient sample. The study also aims to determine the performance (sensitivity and specificity) of the DelApp to discriminate between delirium (with or without dementia) and dementia (without delirium).

The purpose of the Phase C study is to determine the efficacy of the DelApp software application in detecting delirium in unselected patients in an inpatient sample and to determine the performance of the DelApp to discriminate between delirium and dementia. The study also aims to explore the performance of the DelApp in tracking change in cognitive function.

Conditions

Interventions

OTHER

No intervention given to participants

This is an observational study. Participants will receive no intervention.

Sponsors & Collaborators

  • Medical Research Council

    collaborator OTHER_GOV
  • NHS Lothian

    collaborator OTHER_GOV
  • University of Glasgow

    collaborator OTHER
  • NHS Greater Glasgow and Clyde

    collaborator OTHER
  • Cambridge Cognition Ltd

    collaborator INDUSTRY
  • University of Edinburgh

    lead OTHER

Principal Investigators

  • David J Stott · University of Glasgow

  • Elizabeth Wilson · Royal Infirmary of Edinburgh

  • Timothy Walsh · University of Edinburgh

  • Tara Quasim · University of Glasgow

  • Jonathan Evans · University of Glasgow

  • Christopher Weir · University of Edinburgh

  • Alexander Weir · Medical Devices Unit

  • Stuart Parks · Medical Devices Unit

  • Jennifer Barnett · Cambridge Cognition Ltd

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-10-12
Primary Completion
2018-03-22
Completion
2018-03-22

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02590796 on ClinicalTrials.gov