RecruitingNCT06332495

Research Project on the Risk of Discomfort, Pain, Alteration of Skin Condition in Bedpan Use by Patients and Caregivers

Research Project on the Risk of Discomfort, Pain and Alteration of Skin Condition in Bedpan Use by Patients and Caregivers


Sponsor

Nantes University Hospital

Enrollment

300 participants

Start Date

Aug 3, 2024

Study Type

OBSERVATIONAL

Conditions

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

Min Age: 18 Years

Inclusion Criteria8

  • 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 Criteria2

  • Patients with cognitive impairment preventing objective pain assessment or with neurological pathologies.
  • Patients under guardianship, curatorship or safeguard of justice.

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Interventions

OTHERQuestioning the patient during hygiene care

The study examines how patients and caregivers feel when using the bedpan. Over the course of a day, collecting all this information would take just under 7 minutes. Over the duration of patient participation (2 days), we estimate that it would take a total of 15 minutes per patient to collect this information. The objectives are focused on pain and discomfort, and on the alteration of the (patient's) skin condition through objective observation of redness or stage I pressure sores by the caregiver.


Locations(5)

Nantes University Hospital

Nantes, Loire Atlantique, France

CHU Cholet

Cholet, France

CHU Laval

Laval, France

CH Le Mans

Le Mans, France

CHU Orleans

Orléans, France

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NCT06332495


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