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Clinical Trials/NCT06168448
NCT06168448
Completed
Not Applicable

Non Interventional Study Evaluating the Contribution of a Video to Patient Information Before a Complementary Examination in Infectious Diseases

Assistance Publique - Hôpitaux de Paris1 site in 1 country97 target enrollmentDecember 15, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Infectious Disease
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
97
Locations
1
Primary Endpoint
Score of perceived understanding of information before additional examination
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this study is that a video tool coupled with standardized information can increase the patient's understanding of the information and thus optimize their medical care

Detailed Description

Patients admitted to the Infectious and Tropical Diseases Department (MIT) undergo a large number of complementary examinations. In view of their specificity, justified by the often lengthy diagnostic process, as well as by the complexity and diversity of the pathologies, the site of infection and the patient's background (adolescents and adults, migrant patients, immunocompromised patients, Human Immunodeficiency Virus, primary immunodeficiencies, organ transplants, patients with haemopathies, marrow transplants, among others). As a matter of practice, the doctor informs the patient of the prescribed examinations, explaining their purpose and procedure, and outlining any benefits and risks. The intention is to introduce a tool that complements the information usually provided, and that can be of high quality to improve the patient's perception of understanding. To this end, investigators hypothesize that a tool in video format, built in collaboration with the experience of various technical platforms, could make the experience of understanding information more complete and more accessible to all patients.

Registry
clinicaltrials.gov
Start Date
December 15, 2023
End Date
February 14, 2025
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient aged ≥ 18 years
  • French speaking language
  • Hospitalized in the Department of Infectious and Tropical Diseases at Hôpital Necker- Enfants malades
  • Prescription, for the first time in its medical history, of one of the following complementary examinations:
  • Bronchial FibroscopyIRM
  • PICC line insertion
  • PET Scanner
  • No expressed oral opposition

Exclusion Criteria

  • Patients with dementia or cognitive impairment
  • Non-French-speaking patient
  • Caregivers' inclusion Criteria:
  • Caregiver belonging at nurse or doctor's category
  • Caregiver working in the Infectious and Tropical Diseases Department at Necker Hospital
  • No expressed oral opposition
  • Caregivers who are not in contact with patients

Outcomes

Primary Outcomes

Score of perceived understanding of information before additional examination

Time Frame: up to 7 days

Measure the patient's perception of comprehension prior to the examination, using a self-assessment Numerical Scale (NRS) defined from zero (no comprehension) to ten (perfect comprehension). The assessment will be collected by a caregiver who is not in charge of the patient, within a maximum of 24 hours after the carried out examination.

Secondary Outcomes

  • Failure rate of examinations(up to 7 days)
  • Missing elements(up to 7 days)
  • Impact on caregivers' knowledge(1 day)
  • Score of perceived understanding of information after additional examination(up to 7 days)

Study Sites (1)

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