NCT07228767 Assessment of Surgeons' Mental Fatigue Based on Operating Time
| NCT ID | NCT07228767 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Centre Hospitalier Departemental Vendee |
| Condition | Surgical Intervention |
| Study Type | OBSERVATIONAL |
| Enrollment | 8 participants |
| Start Date | 2025-12-05 |
| Primary Completion | 2027-01-05 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 8 participants in total. It began in 2025-12-05 with a primary completion date of 2027-01-05.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
In May 2023, the French National Authority for Health published a solution for patient safety regarding tunnel vision. This concept, which is uncommon in the medical field, is defined as any situation in which a professional's attention is so focused on a goal that they do not hear or see warning signs that should prompt them to change their approach or even stop before an adverse event associated with care occurs. To better understand the causes of medical errors, the research will assess surgeons' mental fatigue and the factors associated with it. This fatigue, which occurs after or during prolonged periods of intense cognitive activity, is associated with a temporary inability to maintain optimal cognitive performance. Assessing mental fatigue is crucial in surgeons, as it can directly affect their ability to perform complex procedures and make critical decisions. The aim of this research is to examine the factors that may influence the level of mental fatigue and cognitive load in surgeons during surgical procedures.
Eligibility Criteria
Inclusion Criteria: * Surgeon working in the digestive surgery department at CHD Vendée * Surgeon capable of understanding the protocol and willing to participate in the research Exclusion Criteria: * Surgeon unable to be available for the entire duration of the research
Contact & Investigator
Emeric ABET
PRINCIPAL INVESTIGATOR
Centre Hospitalier Départemental Vendée
Frequently Asked Questions
Who can join the NCT07228767 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Surgical Intervention. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07228767 currently recruiting?
Yes, NCT07228767 is actively recruiting participants. Contact the research team at promotion.urc@chd-vendee.fr for enrollment information.
Where is the NCT07228767 trial being conducted?
This trial is being conducted at La Roche-sur-Yon, France.
Who is sponsoring the NCT07228767 clinical trial?
NCT07228767 is sponsored by Centre Hospitalier Departemental Vendee. The principal investigator is Emeric ABET at Centre Hospitalier Départemental Vendée. The trial plans to enroll 8 participants.