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Clinical Trials/NCT05378789
NCT05378789CompletedNot Applicable

Appropriation and Impact of the Introduction of Naps During Night Work by Intensive Care Caregiver - One Year Review

Centre Hospitalier Departemental Vendee2 sites in 1 country68 target enrollmentStarted: May 30, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
68
Locations
2
Primary Endpoint
Nap appropriation

Study Overview

Brief Summary

MARIENAIE study is a pilot study on the feasibility and appropriation of nocturnal naps by a team of paramedical caregivers alternating a 12-hour day/night work rhythm for a period of 1 year. To date no study on the impact of nap in ICU on a long period was published.

This study will also explore : the factors favouring or hindering the implementation of this strategy and its maintenance over time through a concomitant sociological qualitative study, the evolution over time of the parameters of perceived nocturnal sleepiness and the immediate impact of the realization of naps on this sleepiness and the evolution over time of the medium-term impact with the help of questionnaires exploring various dimensions concerning the working conditions and health (somatic health, stress, psychosocial risks, evaluation of the working environment).

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Paramedic working 12 hours alternating day and night in the ICU department of the Vendee departmental hospital center.

Exclusion Criteria

  • Pregnant woman.
  • Caregiver with knowledge of a scheduled departure from the ICU within 2 months after the start of the project.
  • Caregiver refusing to participate in the project.

Outcomes

Primary Outcomes

Nap appropriation

Time Frame: 12 months after baseline

Proportion of the number of nights worked with micro-naps to the number of nights worked by a caregiver over a year.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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