NCT06332495 Research Project on the Risk of Discomfort, Pain, Alteration of Skin Condition in Bedpan Use by Patients and Caregivers
| NCT ID | NCT06332495 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Nantes University Hospital |
| Condition | Nurse-Patient Relations |
| Study Type | OBSERVATIONAL |
| Enrollment | 300 participants |
| Start Date | 2024-08-03 |
| Primary Completion | 2026-08-01 |
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 300 participants in total. It began in 2024-08-03 with a primary completion date of 2026-08-01.
⚠ 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
The hypothesis is that the current bedpan is not adapted to the diversity of patients encountered. It is necessary to collect the opinions of patients themselves on the current pool in different departments in order to validate our hypothesis. The objective is to evaluate pain in patients with reduced or very reduced mobility caused by the bedpan currently used in current practice through an observational study.
Eligibility Criteria
Inclusion Criteria: * Patient of legal age (age ≥ 18 years). * Patient with reduced and very reduced mobility, bedridden requiring the use of a bedpan. * Estimated length of hospital stay on the ward ≥ 2 days. * Patient affiliated to a social security system. * Patient able to understand the protocol. * Patient having given oral non-opposition to participate. * Patient who has received the study information note. * Patient who had never participated in this study. Exclusion Criteria: * Patients with cognitive impairment preventing objective pain assessment or with neurological pathologies. * Patients under guardianship, curatorship or safeguard of justice.
Contact & Investigator
Pia SECHER
PRINCIPAL INVESTIGATOR
Nantes University Hospital
Frequently Asked Questions
Who can join the NCT06332495 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Nurse-Patient Relations. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06332495 currently recruiting?
Yes, NCT06332495 is actively recruiting participants. Contact the research team at jules.galy@chu-nantes.fr for enrollment information.
Where is the NCT06332495 trial being conducted?
This trial is being conducted at Nantes, France, Cholet, France, Laval, France, Le Mans, France and 1 additional location.
Who is sponsoring the NCT06332495 clinical trial?
NCT06332495 is sponsored by Nantes University Hospital. The principal investigator is Pia SECHER at Nantes University Hospital. The trial plans to enroll 300 participants.