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NCT04811183 Clinical Trial

Pharmaceutical Consultation and Exchange Between the Pharmacy and the Hospital

Diabetes Clinical Trial

— EPHET  

Official title:
Pharmaceutical Consultation and Exchange Between the Pharmacy and the Hospital

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04811183
Other study ID # 69HCL21_0197
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 4, 2021
Est. completion date December 2021

Study information
Verified date July 2021
Source Hospices Civils de Lyon
Contact Xavier DODE
Phone 04 72 35 71 08
Email xavier.dode@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Investigators hypothesize that the implementation of a hospital pharmacy consultation and the transmission of its report to pharmacies may improve knowledge, adherence and encourage the development of pharmacist medication reviews. A before-and-after study of the implementation of pharmaceutical consultations will allow the investigators to evaluate the validity of the hypothesis.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patient admitted in the endocrinology service for a type 2 Diabetes who has more than 5 concomitant treatments - Adult patient that is being discharged for a return home - Good comprehension of French Exclusion Criteria: - Bad comprehension of French

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Pharmaceutical consultation
Selection of patients for a pharmaceutical consultation with collection of non-opposition and scheduling of telephone interviews or by teleconsultations at one week after hospitalization. Data collection through interviews using a telephone questionnaire (or by teleconsultation) one week after consultation. Elements on knowledge and adherence of treatment will be collected.

Locations
Country Name City State
France Hôpital Louis Pradel Bron

Sponsors (1)
Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Evolution in the knowledge about the patient's condition Treatment knowledge, knowledge about the pathology and knowledge of hygienic and dietary measures will be assessed with a questionnaire giving a score from 0 to 2 -the higher the score, the better the outcome-.
Comparison of the knowledge of the treatment between the first questionnaire conducted during the pharmaceutical consultation and the second questionnaire one week after the consultation.
Statistical evaluation by comparative tests between the two questionnaires.		 One week
Primary Evolution in the adherence Evaluation of the patient's adherence to his treatment through a questionnaire giving a score between 0 to 6 -the higher the score, the better the outcome-. Comparison of the scores between the first questionnaire conducted during the pharmaceutical consultation and the second questionnaire one week after the consultation.
Statistical evaluation by comparative tests between the two questionnaires.		 One week
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