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Impact of Four Patient Information Leaflets (PIL) on Patient Behaviour

Grenoble Alpes University Hospital Center (CHU) logo

Grenoble Alpes University Hospital Center (CHU)

Status and phase

Completed
Phase 4

Conditions

Gastroenteritis
Pharyngitis

Treatments

Procedure: usual consultation
Procedure: Patient Information Leaflets

Study type

Interventional

Funder types

Other

Identifiers

NCT01398696
n° IRB 5891

Details and patient eligibility

About

To assess the impact of four Patient Information Leaflets (PIL) on patient behaviour in primary care.

Full description

A patient who visited, for a gastroenteritis or a pharyngitis, one GP of the intervention group, received a Patient Information Leaflets (PIL) related to his disease and his age: either the gastroenteritis leaflet for adult or the one for child, either the pharyngitis leaflet for adult or the one for child.

Enrollment

400 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patient.
  • Minor child accompanied by a responsible adult.
  • The patient or the caregiver must be reachable by telephone within ten to fifteen 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

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

400 participants in 2 patient groups, including a placebo group

Patient Information Leaflets
Active Comparator group
Description:
Patient Information Leaflets (PIL) is given to the patient during consultation
Treatment:
Procedure: Patient Information Leaflets
usual consultation without PIL
Placebo Comparator group
Description:
no particular intervention during consultation for the patient.
Treatment:
Procedure: usual consultation

Trial contacts and locations

23

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Data sourced from clinicaltrials.gov

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