Working With Your Body in the Operating Room. The Case of Operating Room Nurses (RCIBO)
NCT ID: NCT06938594
Last Updated: 2025-04-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ENROLLING_BY_INVITATION
60 participants
OBSERVATIONAL
2025-01-27
2028-11-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Improvement of Intraoperative Behavior of Staff to Prevent Postoperative Complications
NCT03158181
Management of Perioperative Anxiety by the Cardiac Coherence Technique Coupled With a Hypnosis Session
NCT03981731
Identifying Good and Poor Surgical Behaviour in the Danish Operating Room
NCT01334411
Disruptive Behavior in the Operating Room
NCT05113147
Improved Rehabilitation After Surgery and Hypnosis: Benefits Potentiated by a Preoperative Consultation
NCT05276882
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Student nurses and operating room nurses
* Supervisors
* Doctors, interns and externs
* Surgeons
* Midwives and midwifery students
* Hospital cleaning staff
* Nursing assistants
* Biomedical staff
Exclusion Criteria
* People refusing to take part in the study
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Brest
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Chu Brest
Brest, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
29BRC24.0311 - RCIBO
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.