Stress of Anesthesia Professionals in the Operating Room

Stress Clinical Trial

— StressBloc  

Official title:

Stress of Anesthesia Professionals in the Operating Room

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05392972
• Other study ID #: IRB 00010254 - 2022 - 055
• Status: Completed
• Start date: June 1, 2022
• Est. completion date: December 12, 2022

Study information

• Verified date: December 2022
• Source: University Hospital, Grenoble
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The objective of this study was to determine whether there was an association between the resilience of anesthesia professionals in the operating room of the Grenoble University Hospital and perceived work-related stress.

Description:

This trial will be conducted at the Grenoble Alpes University Hospital (CHUGA). Volunteer anesthesiologists, anesthesia interns, nurse anesthetists and nurse anesthetist students will answer questionnaires evaluating resilience, perceived stress in the last month, sleep quality, number of hours worked in the month, number of night hours and will evaluate each working day the perceived stress with the visual analogical scale of stress over 3 periods of the working day

The main objective is to determine if there is an association between the resilience (questionnaire: Connord davidson resielience scale: CDRISC10) of the anesthesia professionals in the block of the CHUGA and the perceived stress at work (Perceived stress sacle 10: PSS10).

The secondary objectives are to study the association between:

1. The mean of the two stress VAS (at the beginning and end of the shift) collected and the PSS10 over the same period.

2. The median of the peaks of stress VAS collected and the PSS10 over the same period.

3. The PSS10 and the PSQI (Pittsburgh Sleep Quality Index)

4. The PSS10 and the number of hours worked in the month.

5. The PSS10 and the number of night hours worked in the month.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 74
• Est. completion date: December 12, 2022
• Est. primary completion date: December 12, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• resident in anaesthesiology, Anesthesiologist,anaesthetic nursing student, anaesthetic nurse graduated

Criteria for non-inclusion:

• Professionals objecting to the use of their data in the the research

• Professionals working part-time

• Professionals who had a number of CA > 3 during the month of the study.

Related Conditions & MeSH terms

• Stress

Intervention

Behavioral:
• Assessment of stress, resilience and associated factors in anesthesia professionals
Assessment of stress, resilience and associated factors in anesthesia professionals

Locations

Country	Name	City	State
France	University Hospital Grenoble	Grenoble

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Resilience	Measurement of resilience by Connor-Davidson Resilience Scale 10 (CD RISC 10 from 0 to 40) in participants. A high score indicates better resilience.	at day 0
Primary	Perceived Stress Scale	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	Self-reported stress at the beginning of the workday.	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.
Secondary	Self-reported stress at the end of the workday.	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.
Secondary	Maximum self-reported stress of the workday.	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.
Secondary	The score of the Pittsburgh Sleep Quality Index (PSQI)	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
Secondary	number of hours worked	number of hours worked during the working day	Each work day at the end of the service. From day 0 to day 30.
Secondary	number of hours worked at night	the number of hours worked during the work night	Each night of work at the end of the service. From day 0 to day 30.