National Study of a Pharmacokinetic-Focused Educational Package for Patients With Severe Haemophilia A

Hemophilia A Clinical Trial

— UK-PK  

Official title:

UK-PK Study: National Study of the Implementation of a Pharmacokinetic-Focused Educational Package for Patients Living With Severe Haemophilia A

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02528968
• Other study ID #: 2015-MED-13
• Status: Completed
• Phase: N/A
• First received: July 17, 2015
• Last updated: February 21, 2018
• Start date: September 2015
• Est. completion date: November 30, 2017

Study information

• Verified date: February 2018
• Source: Hampshire Hospitals NHS Foundation Trust
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Prospective, interventional study of pharmacokinetic (PK)-focused FVIII dosing discussions delivered as part of a patient education package.

The study will capture severe haemophilia A patient reported outcome measures before and after PK-focused dosing discussions, including a standardised patient education package, that include personalised PK-guided dosing suggestions from a computational predictive device (myPKFiT®). The pragmatic study design recognises the CE marked myPKFiT® device is being implemented into routine care nationally and consequently only requires a single additional clinic visit for the purpose of consenting.

Description:

There is a paucity of patient reported outcome data documenting the impact of PK focused prophylaxis discussions. This prospective, multicentre UK-PK trial will coincide with the initiation of the myPKFiT® device in the context of an enhanced clinical review. This will include a standardised patient education package using a short animated film explaining PK and personalised prophylaxis, followed by modelling of the patient's own PK using the myPKFiT® device and discussing the dosing options with the patient. The aim of the PK educational package is to educate and engage patients and ensure that their treatment regimens meet their individual needs. In addition, the study will capture the prophylaxis dosing strategy agreed upon by patients and the clinical team where treatment decisions are made jointly between patients and the clinical team (concordance). Looking forward, haemophilia clinical care team members need a marker to judge or predict patient engagement with this personalising medicine process. Successful consultation strategies may differ if the team can anticipate how an individual person with haemophilia (PWH) might respond to discussions about potential change. The primary outcome measure is the Patient Activation Measure (PAM) which gauges the knowledge, skills and confidence essential to managing one's own health and healthcare. A PAM score can predict healthcare outcomes including medication adherence, healthcare utilisation and hospital visits. It is hypothesized that a more activated patient will be more receptive to changes in their treatment regimen, education and information about their health condition.

In addition to patient activation, the study will assess a range of patient reported outcomes and psychological factors using validated tools. These will include patients' Haemophilia-related quality of life (HAEMO-QoL-A), beliefs about medicines (BMQ), self-reported adherence (VERITAS-Pro) and activity levels. These tools will provide clear patient reported outcomes for the haemophilia community, with accompanying EQ5D data, enabling robust health economic evaluation.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 59
• Est. completion date: November 30, 2017
• Est. primary completion date: November 30, 2017
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age = 18 years

• Severe haemophilia A (FVIII:C < 1IU/dL)

• Prescribed regular prophylactic treatment (= 2 infusions/week) with Advate® for = 6 months at the time of screening

• Able to give informed consent and willing to participate in this study

Exclusion Criteria:

• Age <18 years

• Non-severe haemophilia A (FVIII:C 1-40IU/dL)

• Weight >120kg

• Treatment with any other FVIII concentrate (recombinant or plasma-derived) during the study period or 6 months prior to screening.

• Receiving on-demand or <6 months of prescribed prophylaxis with Advate®

• Current FVIII inhibitor (> 0.6BU/mL)

• Current immune tolerance induction

• Not able to give informed consent (incapacitated or vulnerable adults)

• Patients with a life expectancy of less than one year

• Already had personalized PK prediction using the myPKFiT®

• Any inclusion criteria not met

Related Conditions & MeSH terms

• Hemophilia A

Intervention

Behavioral:
• Educational Package
Patients will be invited to attend a PK educational session as part of the study protocol. This will form a discussion regarding clinical history and activity in the 6 months prior to study start, viewing of a short animated film giving additional detail on pharmacokinetics and prophylaxis in haemophilia A, followed by modelling of the patient's own PK and dose guidance based on 2 study blood samples.

Locations

Country	Name	City	State
United Kingdom	Barts and The Royal London Hospital	London

Sponsors (1)

Lead Sponsor	Collaborator
Hampshire Hospitals NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Patient Activation Measures	Change in the Patient Activation Measure (PAM) score over a 12 month time period.	12 months
Secondary	Patients' perceptions of the PK educational package	Perceived threat, message quality, message acceptance/derogation. This will be measured qualitatively.	12 months
Secondary	Health-related quality of life: EQ5D		12 months
Secondary	Health-related quality of life: HAEMO-QoL-A		12 months
Secondary	Self-reported adherence (VERITAS-pro)		12 months
Secondary	Health-related quality of life: beliefs about medicines (BMQ)		12 months
Secondary	Changes to participants' treatment regimen	Change to amount of FVIII used	12 months
Secondary	Changes to accuracy and timeliness of entries on treatment log (Haemtrack or alternative treatment log).		12 months
Secondary	Changes to patient adherence to treatment regimen	Actual changes as recorded on Haemtrack / equivalent.	12 months