- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05867238
Impact of Stress Management Training on the Resilience and Stress of Student Nurse Anaesthetists
Study Overview
Status
Conditions
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:
- 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)
- 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)
- 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).
- 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).
- 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
Enrollment (Actual)
Contacts and Locations
Study Locations
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Grenoble, France, 38000
- university grenoble hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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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.
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|
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Student nurse anaesthetists with training in stress management
Volunteer nurse anaesthetist students who have received training in stress management this year.
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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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Stress Scale 10
Time Frame: at day 30
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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.
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at day 30
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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.
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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%).
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Each work day at the start of the shift. From day 0 to day 30.
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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.
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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%).
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Every working day at the end of the shift. From day 0 to day 30.
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Maximum self-reported stress of the workday.
Time Frame: Every working day at the end of the shift. From day 0 to day 30.
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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%).
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Every working day at the end of the shift. From day 0 to day 30.
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The score of the Pittsburgh Sleep Quality Index (PSQI)
Time Frame: at day 30
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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).
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at day 30
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Resilience
Time Frame: at Day 0
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Measurement of resilience by Connor-Davidson Resilience Scale 10 (CDRISC10 from 0 to 40) in participants.
A high score indicates better resilience.
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at Day 0
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overall satisfaction with the stress management training received
Time Frame: at day 30
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Scale from 0 to 10 or a higher score indicates a higher level of satisfaction.
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at day 30
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Have you implemented any of the stress management methods proposed during the training?
Time Frame: at day 30
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Yes or No (qualitative)
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at day 30
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What method of stress management is used?
Time Frame: at day 30
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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
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at day 30
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If you used stress management methods: how frequently?
Time Frame: at day 30
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choice among : Daily,Weekly,Monthly,The day before an exam,During training periods
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at day 30
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Julien Picard, University Hospital, Grenoble
- Principal Investigator: Yoann Zafiriou, University Hospital, Grenoble
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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