Impact of Six Patient Information Leaflets (PIL) on Doctor Patient Communication (EDIFIP)

Floralis

Status and phase: Completed; Phase 4

Conditions: Ankle Sprain; Prostatitis; Pneumonitis; Infectious Colitis; Pyelonephritis; Diverticulitis

Treatments: Procedure: Patient Information Leaflet (PIL)

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT02246361

N°IRB 5891

Details and patient eligibility

About

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.

Full description

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.

Enrollment: 211 patients

Sex: All

Ages: 15+ years old

Volunteers: No Healthy Volunteers

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.

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.

Trial design

Primary purpose: Supportive Care

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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211 participants in 2 patient groups

Phase 1 (without PIL)

No Intervention group

Description:

No particular intervention during consultation for the patient

Phase 2

Experimental group

Description:

Patient Information Leaflet is given to the patient during the consultation

Treatment:

Procedure: Patient Information Leaflet (PIL)