Trials Sponsors Conditions Drugs Pricing

Conditions

Burnout, Professional Cognition Disorders Sleep Deprivation

Keywords

sleep deprivationinternal medicine residencyon callcognitive impairmentburn outsafetydepression

Outcome Measures

Primary Outcomes (6)

Neurological evaluation using Paced Auditory Serial Addition Test (PASAT)
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
Maslach questionaire filled by participant
through study completion, an average of one year
Conners Continuous Performance Test 2 (CPT)
Post on-call attention test
Immediately after a 24 hours on call period, wth a maximum delay of 6 hours after night shift end.

Eligibility Criteria

Sexall

Healthy VolunteersYes

Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

Internal Medicine residents in formation who were on the second or third year of the Internal Medicine residency of the Italian Hospital of Buenos Aires who work 24 hours shifts and whose work day continues to a maximum of 36 total hours and who consented to the study.

You may qualify if:

Internal Medicine residents on the second or third year of formation.

You may not qualify if:

Sponsors & Collaborators

Hospital Italiano de Buenos Aires
Otherlead

Study Sites (1)

Hospital Italiano de Buenos Aires, Peron 4190

Buenos Aires, Buenos Aires F.D., C1199ABB, Argentina

MeSH Terms

Conditions

Sleep DeprivationBurnout, ProfessionalCognition DisordersCognitive DysfunctionBurnout, PsychologicalDepression

Condition Hierarchy (Ancestors)

DyssomniasSleep Wake DisordersNervous System DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsMental DisordersOccupational StressOccupational Diseases

Study Officials

Diego H Giunta, MD
Hospital Italiano de Buenos Aires
STUDY CHAIR

Enrollment

100 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: OTHER
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

October 26, 2016

First Posted

August 12, 2019

Study Start

August 8, 2019

Actual (reported)

Cognitive Performance After a Night Shift in Internal Medicine Residents

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

First Submitted

Study Start

Primary Completion

Study Completion

First Posted

Conditions

Keywords

Outcome Measures

Primary Outcomes (6)

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Secondary Outcomes (1)

Data Sharing

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

Study Start

Primary Completion

Study Completion

First Posted

Conditions

Keywords

Outcome Measures

Primary Outcomes (6)

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Secondary Outcomes (1)

Data Sharing

Source record

Locations