Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Sleep Detection in Residents of Long-term Care Facilities

Sleep Detection in Older Adults Living in Long-term Care Facilities: An Inter-rater Reliability Agreement Study

Sleep disorders are common among older people. People who suffer from sleep disorders typically have difficulty falling asleep, staying asleep, wake up early and do not get restful sleep.

Research on sleep disorders in humans is already underway. Previous research projects in humans have shown that sleep disorders have an impact on bodily functions and quality of life. Disruptions to the sleep-wake cycle can also affect memory. Previous research projects have examined the measurement differences between polysomnography, an overnight sleep measurement in a sleep laboratory, which is currently the gold standard, and various contactless sleep sensor systems. The measurement differences are minor to moderate. However, the investigators do not yet know how large the difference is between different days when using contactless sleep sensor systems in order to determine the accuracy of such devices for residents in retirement and nursing homes.

In this research project, the investigator are therefore investigating sleep variability over a period of 14 days in 52 residents of retirement and nursing homes in Switzerland in order to be able to assess the smallest detectable difference in sleep quality.

The investigators are conducting this research project in accordance with Swiss law. The investigators also comply with all internationally recognized guidelines. The responsible ethics committee has reviewed and approved the research project.

Studieoversikt

Status

Rekruttering

Detaljert beskrivelse

Insomnia is a common sleep problem among older adults, with an overall prevalence reported between 30% and 50% and an even higher value among those living in nursing homes. Symptoms such as difficulty in falling asleep, difficulty in maintaining sleep, early morning awakening and non-restorative sleep not only have an important impact on the functional status and quality of life in older adults, but disturbances of the sleep-wake cycle are also known to be associated with cognitive decline. Polysomnography (PSG) is the current gold standard measuring for sleep disturbances using a collection of surface electrodes, physiologic an sleep parameters (including brain dynamics of electroencephalography (EEG)) in a sleep laboratory overnight. However, a 24-hour sleep detection based on objective measurement in older adults is of importance because excessive daytime sleepiness, and excessive napping are associated with negative health outcomes such as accelerated cognitive decline. Furthermore, Canadian 24-hours movement guidelines recommend to detect movement behavior, with sleep as a movement behavior included, over a 24-hour time span. Contactless sleep technologies (CSTs) may offer a low-burden and feasible assessment to monitoring sleep over 24-hours in older adults. To date there are several CSTs available with differences in accuracy compared to PSG. However, little is known regarding smallest detectable difference based on test-retest analysis based on intraday variability to effectively test the accuracy of such devices in older adults living in long-term care facilities. The objective of this study is to evaluate the smallest detectable difference of sleep quality based on test-retest analysis of two CSTs: (i) the Withings Sleep Analyzer and (ii) the Sleepiz One+ hardware in older adults.

Studietype

Observasjonsmessig

Registrering (Antatt)

52

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

    • St.Gallen
      • Sankt Gallen, St.Gallen, Sveits, 9001
        • Rekruttering
        • Easternswiss University of Applied Sciences

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

Older Adults living in long-term care facilities without any neurocognitive disorder

Beskrivelse

Inclusion Criteria:

  • Signed informed consent
  • Older adults living in the long-term care facilities

Exclusion Criteria:

  • Neurocognitive disorders based on Alzheimer's Disease, Parkinson's disease, Lewy body dementia or Mixed dementia according to patient record

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
residents of long-term care facilities without any neurocognitive disorders
residents of long-term care facilities without any neurocognitive disorders according to patient record

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Total Sleep Time
Tidsramme: From enrollment to 14 days after
The time a person lying in bed actually sleeping
From enrollment to 14 days after

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Eling D de Bruin, Prof. Dr., Eastern Swiss University of Applied Sciences, ETH Zruich

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

28. august 2025

Primær fullføring (Antatt)

1. februar 2027

Studiet fullført (Antatt)

1. august 2027

Datoer for studieregistrering

Først innsendt

9. september 2026

Først innsendt som oppfylte QC-kriteriene

9. september 2026

Først lagt ut (Faktiske)

14. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

17. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

15. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • SleepDetection
  • 2025 (U.S. NIH-stipend/kontrakt: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
  • 2025-00629 (Registeridentifikator: Eastern Swiss Ethics Committee)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere