Translation and Validation of the French Version of the Sleep Regularity Questionnaire: a New Tool to Address the the Challenge of Sleep Health

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Bordeaux

About this trial

Sleep is an essential function for physical and mental health. The mismatch between biological rhythms and the social rhythms of individuals is increasingly common in modern societies. This sleep irregularity can have numerous consequences on mental health, cardiometabolic health, the immune system, functioning, and quality of life. To address the public health issue of sleep irregularity, it is important to be able to obtain a valid and reliable measure. The Sleep Regularity Questionnaire (SRQ) by Dzierzewski et al. addresses this issue, but has never been translated into French. The aim of the study is to translate and validate the French version of the Sleep Regularity Questionnaire.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient ≥ 18 years of age

Patient with indication for 14-day actimetry for chronic insomnia or circadian rhythm disorder

Patients with an indication for 14-day actimetry to assess sleep-wake rhythms, for example prior to a 36-hour polysomnographic recording to diagnose central hypersomnia (narcolepsy or idiopathic hypersomnia).

Patient affiliated to or benefiting from a social security scheme

Disqualifiers

Current psychiatric disorder (mood disorders, anxiety, psychosis, sleep-interfering use disorder) assessed during interview with investigator

Current neurological disorder affecting sleep (neurodegenerative disease, stroke, epilepsy) assessed during interview with investigator

Unstable cardiovascular or respiratory diseases

Pregnant or breast-feeding women

Trial population

French patients indicated for 14-day actimetry for chronic insomnia or circadian rhythm disorders

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • SRQ questionnaire

    Other intervention

    SRQ questionnaire administered at inclusion visit and 14 days after inclusion

Treatment groups

50 Participants
are divided into 1 treatment group
Group A: Patients1 intervention

Trial outcomes

Primary outcomes

1

Internal validity

consistency measured by Cronbach's alpha and exploratory and confirmatory factor analysis

Time frame
At day 14 after inclusion

Secondary outcomes

1

Insomnia

measured by the Insomnia Severity Index

Time frame
at inclusion (day 0)
2

Sleepiness

measured by the Epworth Sleepiness Scale

Time frame
at inclusion (day 0)
3

Depression and anxiety

measured by the Patient Health Questionnaire-4

Time frame
at inclusion (day 0)
4

Chronotype

measured by the Morningness-Eveningness Scale Short Version

Time frame
at inclusion (day 0)

Other outcomes

Sponsors and contacts

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