Impact of Six Patient Information Leaflets (PIL) on Doctor Patient Communication
NCT ID: NCT02246361
Last Updated: 2015-08-27
Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Recruitment Status
COMPLETED
Clinical Phase
PHASE4
Total Enrollment
211 participants
Study Classification
INTERVENTIONAL
Study Start Date
2014-09-30
Study Completion Date
2015-05-31
Brief Summary
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The purpose of this "before-after" prospective multicenter study is to assess the impact of six Patient Information Leaflets (PILs) on Doctor Patient Communication scale (DPC) and adherence scale for common acute illnesses in emergency ward.
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Detailed Description
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Assessing the impact of six Patient Information Leaflets (PILs) on Doctor Patient Communication scale (DPC) and adherence scale for common acute illnesses (infectious colitis, diverticulitis, pneumonitis, prostatitis, pyelonephritis , ankle sprain) in two emergency ward.
For "before" study without intervention : usual consultation without PIL .
For "after study" with intervention : the patient is given a PIL related to his disease during the consultation.
Data collection will take place the same day as the consultation by self-administered questionnaire for DPC scale and also between 7 to 10 days after the consultation by phone survey for DPC scale and adherence scale.
For "before" study without intervention : usual consultation without PIL .
For "after study" with intervention : the patient is given a PIL related to his disease during the consultation.
Data collection will take place the same day as the consultation by self-administered questionnaire for DPC scale and also between 7 to 10 days after the consultation by phone survey for DPC scale and adherence scale.
Conditions
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Ankle Sprain
Infectious Colitis
Diverticulitis
Pyelonephritis
Prostatitis
Pneumonitis
Study Design
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Allocation Method
NON_RANDOMIZED
Intervention Model
PARALLEL
Primary Study Purpose
SUPPORTIVE_CARE
Blinding Strategy
SINGLE
Participants
Study Groups
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Phase 1 (without PIL)
No particular intervention during consultation for the patient
Group Type
NO_INTERVENTION
No interventions assigned to this group
Phase 2
Patient Information Leaflet is given to the patient during the consultation
Group Type
EXPERIMENTAL
Patient Information Leaflet (PIL)
Intervention Type
PROCEDURE
Patient Information Leaflet (PIL) about infectious colitis, diverticulitis, pneumonitis, prostatitis or either pyelonephritis is given to the patient related to his disease during the consultation
Interventions
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Patient Information Leaflet (PIL)
Patient Information Leaflet (PIL) about infectious colitis, diverticulitis, pneumonitis, prostatitis or either pyelonephritis is given to the patient related to his disease during the consultation
Intervention Type
PROCEDURE
Eligibility Criteria
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Inclusion Criteria
* Adult patient.
* Minor aged over 15 years accompanied by a responsible adult.
* The patient must be reachable by telephone within seven to ten days following the consultation.
* Minor aged over 15 years accompanied by a responsible adult.
* The patient must be reachable by telephone within seven to ten days following the consultation.
Exclusion Criteria
* Illiterate patient.
* Patient refusing follow-up call.
* Patient with visual or hearing impairment.
* Patient non-Francophone.
* Private patient of liberty by judicial or administrative.
* Person being a measure of legal protection.
* Patient refusing follow-up call.
* Patient with visual or hearing impairment.
* Patient non-Francophone.
* Private patient of liberty by judicial or administrative.
* Person being a measure of legal protection.
Minimum Eligible Age
15 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
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Groupe Hospitalier Mutualiste de Grenoble
OTHER
Sponsor Role
collaborator
Floralis
INDUSTRY
Sponsor Role
lead
Responsible Party
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Responsibility Role
SPONSOR
Principal Investigators
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Melanie Sustersic, MD
Role: PRINCIPAL_INVESTIGATOR
Floralis France
Locations
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Groupe Hospitalier Mutualiste, service des urgences
Grenoble, Isere, France
Site Status
Centre Hospitalier
Chambéry, Savoie, France
Site Status
Countries
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France
References
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Reference Type
DERIVED
Other Identifiers
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N°IRB 5891
Identifier Type: -
Identifier Source: org_study_id
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