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Evaluating the Validity and Acceptability of a Fully-automated Interview to Diagnose Insomnia Disorder: a Pilot Study

U

University of Bordeaux

Status

Completed

Conditions

Insomnia Disorder

Treatments

Diagnostic Test: mobile health application named KANOPEE

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Objective: to evaluate if a fully-automated diagnostic interview for insomnia disorder is suitable for clinical and research purposes (adequate sensitivity and specificity) and is acceptable to patients.

Study main outcomes:

  1. Concurrent validity (sensitivity and specificity) compared to a gold standard. Gold standard: clinical diagnosis of a clinician using a validated structured clinical interview for the DSM 5 criteria of insomnia disorder
  2. Acceptability of the fully-automated interview.

Participants:

Volunteers to undergo the clinical and the automated interview will be recruited through non-probability convenience sampling from patients attending the sleep clinic at Bordeaux University Hospital between May 2023 and July 2023.

Enrollment

56 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 18 years or older
  • Being able to communicate and read in French
  • Previous use a mobile phone

Exclusion criteria

  • N/A

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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