- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04406220
The Effect of Large Versus Small Clog Size on Emergency Response Time
The Effect of Large Versus Small Clog Size on Healthcare Professional Emergency Response Time: a Randomized Controlled Trial
In many hospitals, clogs, usually white, are provided for healthcare workers. In our hospital, health care professionals from the department of intensive care medicine may be summoned to an emergency situation on a 24/7 basis. Clogs are thought to be of importance for running. Although clogs are available in several sizes, clog size is typically left to the discretion of the individual healthcare worker. Interestingly,
The primary goal of this randomized controlled trial is to assess if wearing large size clogs as compared to small size clogs results in increased running speed.
Participants will be randomized to small versus large clog size using a using randomly permuted blocks stratified by gender. Following randomization, participants will wear the clogs of allocated size and complete a standardized running course.
The primary endpoint is the time taken to complete the course.
The enrolment of 50 subjects would provide 80% power to show a 5-second difference in the response time at an average response time of 30 seconds with a 6 second standard deviation.
The ethical committee judged the study protocol exempt from extensive review.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Amsterdam, Holland, 1081 HV
- Amsterdam Umc, Location Vumc
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Healthcare workers aged 18 years or older.
Exclusion Criteria:
- Inability to run on clogs.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Small clog size
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Participants will be randomized to run in small clogs
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Aktiv komparator: Large clog size
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Participants will be randomized to run in large clogs
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Time to complete the running course
Tidsramme: Follow-up until 60 minutes.
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The time to complete the course will be compared between the two groups using a linear model with the randomized allocation and the stratification variable as covariates.
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Follow-up until 60 minutes.
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Adverse events
Tidsramme: Follow-up until 60 minutes.
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Follow-up until 60 minutes.
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Time to complete the running course for specific subgroups: By gender, job function, level of fitness.
Tidsramme: Follow-up until 60 minutes.
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Follow-up until 60 minutes.
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Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Studiestol: Paul Elbers, MD, PhD, Amsterdam Umc, Location Vumc
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2019-clog
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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