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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05449197
Other study ID # 69HCL21_1391
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2022
Est. completion date January 5, 2023

Study information

Verified date January 2023
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Haemophilia A (HA) is a rare constitutional haemorrhagic disease whose drug management is based on the use of chronic lifelong replacement therapy. The occurrence of an inhibitor is a dreaded complication that impacts conventional management, consisting in using factor VIII (FVIII)-based replacement therapy, most often for prophylaxis. Although effective, these treatments can only be administered intravenously, leading to accessibility constraints and significant mental burden for patients and their relatives. Before June 15, 2021 in France, the emicizumab (HEMLIBRA®) was available only in hospital pharmacies for the prevention or reduction of bleedings. The introduction of the dual dispensing circuit in hospital or community pharmacies, left to patient's choice, is effective from this date. These changes have important organizational consequences for patients and health professionals alongside the pathway of care. Therefore, the effectiveness of this new organization requires to be evaluated with a national French study, called PASO DOBLE DEMI. The aims of this study are twofold : I. To evaluate the direct impact of the training programs provided to the new placeholders of the dispensing circuit ; the community pharmacists, II. To evaluate satisfaction of patients or their relatives regarding the emicizumab treatment whether they chose dispensing in the community pharmacy, or kept the dispensing at the hospital pharmacy. The methodology was based on the 4-level of the Kirkpatrick's evaluation model; 1) the immediate reaction of community pharmacists following the trainings (Reaction), 2) their knowledge acquisition (Learning), 3) their professional practice (Behavior) and 4 ) the patients' satisfaction related to their treatment whether dispensing in hospital or in community pharmacies (Results). The PASO DOBLE DEMI I was based on the first three levels of the evaluation model.


Recruitment information / eligibility

Status Completed
Enrollment 363
Est. completion date January 5, 2023
Est. primary completion date December 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Pharmacists practicing in a pharmacy in metropolitan France - Working in a pharmacy chosen by the patient with haemophilia type A - And who have agreed to dispense Emicizumab (Hemlibra®) Exclusion Criteria: - Other pharmacy staff (including pharmacy technician, biologist, pharmacy students) - Retired pharmacists at the date of the study - Pharmacists who no longer practice in a community pharmacy dispensing Emicizumab (HEMLIBRA®) - Pharmacists who expressed opposition to participating in the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
HEMOPHAR e-learning program
training on professional practice by following HEMOPHAR e-learning program

Locations

Country Name City State
France Hospices Civils de Lyon 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 Number of trained pharmacists dispensing emicizumab (HEMLIBRA (R)) in community pharmacies 6 months.
Primary Number of non-trained pharmacists dispensing emicizumab (HEMLIBRA (R)) in community pharmacies 6 months.
Primary Satisfaction of community pharmacists following the HEMOPHAR training program assessed by a likert scale levels of satisfaction (very satisfied,satisified, dissatisfied,very dissatisfied) 6 months.
Primary Professional practices of community pharmacists in dispensing emicizumab (HEMLIBRA (R)) assessed by a specific questionnaire specific questionnaire developed for the study 6 months.
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