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Clinical Trials/NCT05388344
NCT05388344
Completed
Not Applicable

LUMINA : Measure the Effectiveness of the Booklet Named "Comprendre Les Essais Cliniques" With Patients Included or Not Included in Clinical Trials Within the Clinical Neurosciences - Rheumatology Pole of the CHU de Nice

Centre Hospitalier Universitaire de Nice1 site in 1 country50 target enrollmentOctober 15, 2021
ConditionsRheumatic

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rheumatic
Sponsor
Centre Hospitalier Universitaire de Nice
Enrollment
50
Locations
1
Primary Endpoint
Evaluate the effectiveness of the booklet
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Various studies have shown that many patients do not understand all the information provided by the study investigator and by the information sheet before entering a clinical research protocol. Many materials has been developped in previous research, trying to improve patients' understanding. Nonetheless, their effectiveness remains uncertain.

The "LUMINA" project aims to measure the effectiveness of the booklet named "Comprendre les essais cliniques" with patients included or not included in clinical trials within the Clinical Neurosciences - Rheumatology pole of the CHU de Nice. The design of this study is "before/after". A questionnaire was submitted to the patients before and after reading the booklet. That method is used in order to show if there was a difference between the score obtained from the questionnaire before and after reading. This difference could reflect an improvement in patients' comprehension and, by extension, the effectiveness of the support the team developed.

Registry
clinicaltrials.gov
Start Date
October 15, 2021
End Date
December 15, 2021
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patient coming for a consultation or an hospitalization within the Clinical Neurosciences-Rheumatology pole of the CHU de Nice, or companions/caregivers who helps the patients understand
  • Patient able to read and to understand the french language,
  • Patient included or not in clinical trials.

Exclusion Criteria

  • Participants unable to read
  • Patient unable to understand the french language

Outcomes

Primary Outcomes

Evaluate the effectiveness of the booklet

Time Frame: day 1

Measurement of the score (0 to 13)obtained from the assessment questionnaire (right or wrong) created for the study, before and after reading the booklet right = 1 point, wrong = 0 point . Score: points addition

Secondary Outcomes

  • Assess the difference in understanding between patient groups(day 1)
  • Assess the booklet comprehension(day 1)
  • Assess the booklet's lisibility(day 1)
  • Measurement of the patients' satisfaction(day 1)

Study Sites (1)

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