Validity and Reliability of the French Translation of the Richards-Campbell Questionnaire
NCT ID: NCT06945874
Last Updated: 2025-04-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
190 participants
OBSERVATIONAL
2025-05-01
2026-11-01
Brief Summary
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Detailed Description
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Current management of these disorders remains limited:
* No pharmacological treatment has clearly demonstrated its efficacy on sleep quality in intensive care.
* Interventions aimed at modulating environmental nuisances (reducing noise, reducing light exposure, respecting day/night cycles) have shown limited effects.
* According to the available data, individual devices (eye masks, earplugs) have not significantly improved sleep architecture.
In this context, the Richards-Campbell questionnaire (RCSQ) represents an interesting alternative for subjectively assessing sleep in intensive care patients. This questionnaire, specifically designed for these patients, provides a simple and rapid assessment of sleep disturbances. The validation of a French version of the RCSQ meets a need to standardise assessment practices in France and to gain a better understanding of the factors influencing sleep quality in intensive care.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Interventions
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Validation of sleep quality by the Richards-Campbell Sleep Questionnaire (RCSQ) in french version
The RCSQ questionnaire translated into French (RCSQ-F) will be distributed to intensive care patients who meet the inclusion and non-inclusion criteria and who have given their informed consent to participate in the study.
The questionnaire will be distributed on two occasions: at the first visit and on the day of discharge from intensive care for survivors, or at the latest on the 14th day of hospitalisation.
Patients' use of the questionnaire will enable internal validation (primary objective) by exploratory factor analysis.
Eligibility Criteria
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Inclusion Criteria
* Hospitalised in intensive care for at least 24 hours
* Able to understand and answer questionnaires
* Unsedated (discontinued for 24 hours) presenting a Richmond Sedation Agitation Scale score between ≥-2 and ≤ +1
* Fluent in French
* Having given oral consent for participation in the study
* Person affiliated to a social security scheme.
Exclusion Criteria
* Person deprived of liberty by an administrative or judicial decision or protected adult subject (under guardianship or curatorship)
* Patient unable, for whatever reason, to read, understand or answer the questionnaires (visual problems, psychiatric or cognitive problems, etc.)
* Patient already included in the study or another study evaluating sleep
18 Years
ALL
No
Sponsors
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University Hospital, Rouen
OTHER
Responsible Party
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Principal Investigators
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Marie-Anne MM MELONE, Doctor
Role: PRINCIPAL_INVESTIGATOR
University Rouen Hospital
Locations
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University Hospital of Poitiers
Poitiers, , France
University Rouen Hospital
Rouen, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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IDRCB : 2025-A00224-45
Identifier Type: OTHER
Identifier Source: secondary_id
2025/0017/OB
Identifier Type: -
Identifier Source: org_study_id
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