Impact of Stress Management Training on the Resilience and Stress of Student Nurse Anaesthetists

December 4, 2023 updated by: University Hospital, Grenoble
The study aims to evaluate the effectiveness of stress management training provided to student nurse anaesthetists on: their level of chronic perceived stress in the last month, their level of acute perceived stress each day for one month, their level of resilience and their level of sleep quality.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

This trial will be conducted at the CHU Grenoble Alpes (CHUGA). Volunteer nurse student anaesthetists trained in stress management will complete questionnaires assessing resilience, perceived stress over the past month, sleep quality and will assess perceived stress on each working day using the visual analogue stress scale over 3 periods of the working day.

The results of the trained students will be compared to the results of the untrained students who participated in the Anaesthesia worker stress in the Operating Room survey registered under the clinical trial number: NCT05392972

The main objective is to evaluate the impact of stress management training provided to nurse anaesthetist students on their chronic perceived stress over one month assessed with the Perceived Stress Scale 10.

The secondary objectives are:

  1. To compare the level of resilience of students who have received training in stress management methods with that of students who have not received such training. (Comparison of the average of the Connor-Davidson resilience scale for each population)
  2. Compare the perceived stress during a working day in students who have received stress management training to those who have not. (Comparison of the average of the two visual analogue stress scales (VAS Stress) (start of shift/end of shift) collected on working days over a period of one month for both populations)
  3. Compare the stress peaks experienced (acute stress) by students who have received stress management training and those experienced by students who have not. (Comparison of the median of the stress VAS peaks of the two populations followed over one month).
  4. Determine whether the quality of sleep of the students is influenced by the stress management training (comparison of the pittsburgh sleep quality index (PSQI) of the nurse student anaesthesist population that received stress management training with the PSQI of population that did not receive this training).
  5. Conduct a satisfaction survey among the nurse student anaesthesist regarding the training provided by the Grenoble training institute and identify the stress management methods retained as useful by the nurse student anesthesist following this training.

Study Type

Observational

Enrollment (Actual)

61

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Grenoble, France, 38000
        • university grenoble hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Student nurse anaesthetist from the Grenoble school.

Description

Inclusion Criteria:

  • Student nurse anaesthetist

Exclusion Criteria:

  • Student objecting to the use of their personal information
  • Student on study leave.
  • Student on sick leave during the study period.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Student nurse anaesthetists with no training in stress management
Student nurse anaesthetists who participated in the previous study: stress of anaesthesia professionals in the operating theatre and did not receive stress management training.
Student nurse anaesthetists with training in stress management
Volunteer nurse anaesthetist students who have received training in stress management this year.
The stress management training included 1 day and a half day. It was given by a therapist trained in transactional analysis and a trainer from the nurse anaesthetist school. The training was based on cognitive behavioural stress management training and the use of stress management exercises: cardiac coherence, mindfulness meditation, muscle relaxation, mental imagery.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceived Stress Scale 10
Time Frame: at day 30
The Perceived Stress Scale (PSS10 from 10 To 50) measures the degree to which respondents feel their lives are unpredictable, uncontrollable, and overloaded. A high score indicates more stress.
at day 30

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-reported stress at the beginning of the workday.
Time Frame: Each work day at the start of the shift. From day 0 to day 30.
Stress level self reported by participants on visual analogical scale (VAS from 0 to 100); One end of the scale represents the maximum conceivable symptom strength (i. e., 100%), the other end no symptoms whatsoever (i. e., 0%).
Each work day at the start of the shift. From day 0 to day 30.
Self-reported stress at the end of the workday.
Time Frame: Every working day at the end of the shift. From day 0 to day 30.
Stress level self reported by participants on visual analogical scale (VAS from 0 to 100); One end of the scale represents the maximum conceivable symptom strength (i. e., 100%), the other end no symptoms whatsoever (i. e., 0%).
Every working day at the end of the shift. From day 0 to day 30.
Maximum self-reported stress of the workday.
Time Frame: Every working day at the end of the shift. From day 0 to day 30.
Stress level self reported by participants on visual analogical scale (VAS from 0 to 100); One end of the scale represents the maximum conceivable symptom strength (i. e., 100%), the other end no symptoms whatsoever (i. e., 0%).
Every working day at the end of the shift. From day 0 to day 30.
The score of the Pittsburgh Sleep Quality Index (PSQI)
Time Frame: at day 30
The PSQI contains 19 self-assessed questions. These 19 questions combine to yield 7 components: (1) subjective sleep quality, (2) sleep latency, (3) sleep duration, (4) habitual sleep efficiency, (5) sleep disturbance, (6) use of sleeping medication, and (7) daytime dysfunction. Each component gives a score from 0 to 3 points (0 indicates no difficulty, while 3 indicates major difficulty). The scores of the seven components are then added together to give an overall score of 0 to 21 points (0 indicating no difficulty, and 21 indicating major difficulty).
at day 30
Resilience
Time Frame: at Day 0
Measurement of resilience by Connor-Davidson Resilience Scale 10 (CDRISC10 from 0 to 40) in participants. A high score indicates better resilience.
at Day 0
overall satisfaction with the stress management training received
Time Frame: at day 30
Scale from 0 to 10 or a higher score indicates a higher level of satisfaction.
at day 30
Have you implemented any of the stress management methods proposed during the training?
Time Frame: at day 30
Yes or No (qualitative)
at day 30
What method of stress management is used?
Time Frame: at day 30
choice among: cardiac coherence,self-hypnosis,mental imagery (colourful garden),muscle relaxation,automatic thinking (safe place),rational thinking (autogenic training),breathing meditation, other / free response
at day 30
If you used stress management methods: how frequently?
Time Frame: at day 30
choice among : Daily,Weekly,Monthly,The day before an exam,During training periods
at day 30

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Julien Picard, University Hospital, Grenoble
  • Principal Investigator: Yoann Zafiriou, University Hospital, Grenoble

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 20, 2023

Primary Completion (Actual)

June 15, 2023

Study Completion (Actual)

September 15, 2023

Study Registration Dates

First Submitted

May 5, 2023

First Submitted That Met QC Criteria

May 16, 2023

First Posted (Actual)

May 19, 2023

Study Record Updates

Last Update Posted (Estimated)

December 5, 2023

Last Update Submitted That Met QC Criteria

December 4, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • IRB 00010254 - 2023 - 033

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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