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

Impact of Four Patient Information Leaflets (PIL) on Patient Behaviour : a Randomised Controlled Trial in Primary Care.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01398696
Acronym
PIL
Enrollment
400
Registered
2011-07-20
Start date
2009-11-30
Completion date
2011-01-31
Last updated
2011-10-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastroenteritis, Pharyngitis

Keywords

Patient Information Leaflets, primary care, patient behaviour, pharyngitis, gastroenteritis

Brief summary

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

Detailed 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.

Interventions

Patient Information Leaflets (PIL) about adult gastroenteritis, children gastroenteritis, adult pharyngitis or either children pharyngitis in consultation room

PROCEDUREusual consultation

No particular intervention during consultation for the Patient. No Information Leaflets (PIL) is given

Sponsors

University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
The primary outcome measure was the mean behaviour scoreIn ten to fifteen days after patient after the visitAll patients were called, ten to fifteen days after the visit, to answer a questionnaire on their behaviour related to the disease since they visited the GP. It permitted to calculate a behaviour score. Better was the score, better was the patient's behaviour related to his disease.

Secondary

MeasureTime frameDescription
the mean comprehension scorein ten to fifteen days after the visitAll patients (or their parent) were called, ten to fifteen days after the visit, to answer a questionnaire on their comprehension related to the disease since they visited the GP. It permitted to calculate a comprehension score. Better was this score, better was the patient's comprehension.
number of visit of patient's family for the same pathologyin ten to fifteen days after the visitwe get the information by a phone call to the patient, in ten to fifteen days after the visit

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026