Effects of Relaxing Breathing Combined With Biofeedback on the Performance and Stress of Residents During HFS

NCT04141124 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 156

Last updated 2021-05-18

No results posted yet for this study

Summary

The harmful effects of stress on health professionals are expressed both in terms of their health (physical or mental) and the quality of work (reduced memory capacity, deterioration in patient care). These adverse effects highlight the importance of implementing effective coping strategies and/or early learning of stress management methods in medical training programs.

Relaxation breathing techniques coupled with heart rate variability (HRV) biofeedback is one of the new techniques used to reduce the stress level.

No research has yet tested the effects of HRV induced by relaxation breathing technique before managing a simulated critical situation.

Conditions

  • Stress, Psychological
  • Stress, Physiological
  • Performance Anxiety
  • Critical Incident

Interventions

OTHER

breathing exercise/HRV-biofeedback

5 min of relaxing breathing, coupled with biological feedback.

OTHER

Relaxing Breathing

5 minutes of relaxing breathing guided by a computer helping to follow inspiration and expiration.

OTHER

Control

5 minutes of reading fictitious biological medical results

Sponsors & Collaborators

  • Schlatter, S., Claude Bernard University

    collaborator UNKNOWN
  • Therond, C., Claude Bernard University

    collaborator UNKNOWN
  • Louisy, S., Claude Bernard University

    collaborator UNKNOWN
  • Duclos, A., Claude Bernard University

    collaborator UNKNOWN
  • Guillot, A., Claude Bernard University

    collaborator UNKNOWN
  • Lehot, J-J., Claude Bernard University

    collaborator UNKNOWN
  • Rimmelé, T., Claude Bernard University

    collaborator UNKNOWN
  • Debarnot, U., Claude Bernard University

    collaborator UNKNOWN
  • Lilot, M., Claude Bernard University

    collaborator UNKNOWN
  • Claude Bernard University

    lead OTHER

Principal Investigators

  • Marc Lilot, M.D. · University of Lyon medical center Rockfeller

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-11-01
Primary Completion
2020-06-30
Completion
2020-06-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04141124 on ClinicalTrials.gov