- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT04053556
Cognitive Performance After a Night Shift in Internal Medicine Residents
Evaluation on the Effect on Cognition and Emotional Exhaustion With a Change of Long Night Shift System Versus Reduced Night Shift in Residents of Internal Medicine
Studieoversikt
Status
Detaljert beskrivelse
The investigators conducted a cross sectional study during the 2014-2016 period in a high complexity school hospital in Buenos Aires. Second and third year Internal Medicine residents who consented to participate were included.
A neurologist conducted a cognitive evaluation to the residents who had done 24 hours shifts (with sleep deprivation) within 6 hours of its end.
Auditory memory deficit was evaluated (PASAT - Paced Auditory Serial Addition Test), verbal fluency (FAS), direct and indirect Digit-Span, Rey auditory verbal learning test (RAVLT) and Continuous Performance Test 2 (CPT2).
Results were presented as means of standardized scores (z score) with their interquartile range (IQR).
Studietype
Registrering (Faktiske)
Kontakter og plasseringer
Studiesteder
-
-
Capital Federal
-
Ciudad Autonoma de Buenos Aires, Capital Federal, Argentina, C1199ABB
- Hospital Italiano de Buenos Aires, Peron 4190
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
- Eldre voksen
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
Inclusion Criteria:
- Internal Medicine residents on the second or third year of formation.
Exclusion Criteria:
- Denial to participate in the study or to the informed consent.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Neurological evaluation using Paced Auditory Serial Addition Test (PASAT)
Tidsramme: Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.
|
Post on-call cognition assessment
|
Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.
|
|
Burn Out
Tidsramme: through study completion, an average of one year
|
Maslach questionaire filled by participant
|
through study completion, an average of one year
|
|
Conners Continuous Performance Test 2 (CPT)
Tidsramme: Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.
|
Post on-call attention test
|
Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.
|
|
Rey auditory verbal learning test (RAVLT)
Tidsramme: Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.
|
Post on-call cognition assessment
|
Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.
|
|
F-A-S test
Tidsramme: Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.
|
Post on-call verbal fluency
|
Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.
|
|
Direct and indirect digit span
Tidsramme: Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.
|
Post on-call short-term verbal memory
|
Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Depression
Tidsramme: through study completion, an average of one year
|
Questionaire filled by participant
|
through study completion, an average of one year
|
Samarbeidspartnere og etterforskere
Etterforskere
- Studiestol: Diego H Giunta, MD, Hospital Italiano de Buenos Aires
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 2489
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
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