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Impact of Stress and Sleep Management on Emergency Professionals (REST)

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Completed

Conditions

Healthy

Treatments

Behavioral: recovery management program

Study type

Interventional

Funder types

Other

Identifiers

NCT05251246
69HCL21_0774
2021-A02218-33 (Other Identifier)

Details and patient eligibility

About

The investigators hypothesize that a recovery management program could have an impact on emergency nurses and physicians by improving their sleep and reducing their psychological and physiological responses when dealing with stressful situations during their professional practice. The REST study consists in developing a recovery management program for emergency professionals. The following strategies would be proposed :

  • sleep management according to their schedules by anticipation and recovery,
  • stress management through cardio-feedback techniques (cardiac coherence) also called controlled breathing techniques and mental imagery.

The objectives are to evaluate the impact of this program on the physiological and psychological stress of the emergency professionals during their professional activity, as well as on their sleep. To do so, their respiratory and heart rates, as well as their activity and resting times will be recorded continuously for one week. At the end of each shift, the emergency professionals will report and evaluate the 3 most stressful events.

Enrollment

72 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Nurses or physicians
  • In current position for at least one year
  • Full time or minimum three shifts per week
  • Location: Emergency Department of the Edouard Herriot Hospital or the South Lyon Hospital
  • Free and informed consent

Exclusion criteria

  • Caregivers on leave during the enrollment period
  • Pregnant, parturient or breastfeeding caregivers
  • Participation in another study

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

72 participants in 2 patient groups

Without recovery management program
No Intervention group
Trained in the recovery management program
Experimental group
Description:
Half of the included volunteered participants are randomized in the intervention group
Treatment:
Behavioral: recovery management program

Trial contacts and locations

1

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Central trial contact

Stéphanie MAZZA, Prof; Marion DOUPLAT, MD

Data sourced from clinicaltrials.gov

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