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Assessment of the Effectiveness of IV and SC Abatacept (Orencia) Patient Alert Cards in Patients With Rheumatoid Arthritis in a Sample of EU Countries

Evaluation of the Effectiveness of the Abatacept (Orencia®) IV and SC Patient Alert Cards in Patients With Rheumatoid Arthritis in European Economic Area Countries

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02632890
Enrollment
203
Registered
2015-12-17
Start date
2016-11-29
Completion date
2017-04-28
Last updated
2017-06-16

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

Conditions

Rheumatoid Arthritis

Brief summary

The purpose of the study is to determine a) if the implementation of abatacept (Orencia®) patient alert card (PAC) resulted in effective understanding of key safety messages and b) if the degree of understanding of key safety messages is associated with improved clinical and safety outcomes.

Detailed description

3 sub studies: 2 Cross-Sectional and 1 retrospective chart review

Interventions

None listed

Sponsors

Bristol-Myers Squibb
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient survey (cohort 1): 1. Patients has taken abatacept within the previous 3 months for rheumatoid arthritis 2. Patient is 18 years of age or over * HCP survey (cohort 2): a) Physician or nurses working in rheumatology centers, with at least 1 patient taking abatacept in the previous 6 months for rheumatoid arthritis (by prescribing, administering or by follow up) * Retrospective chart review study (cohort 3): 1. Patient survey questionnaire completed , Informed Consent Form (ICF) signed

Exclusion criteria

* Patient survey: 1. Patient has participated in a clinical trial for their arthritis in the previous 12 months 2. Currently an employee of BMS * HCP survey: 1. Physicians or nurse who have recruited patients for the Patient survey 2. Currently an employee of BMS

Design outcomes

Primary

MeasureTime frameDescription
Retrospective chart review study (clinical outcome study): Proportion of infections leading to hospitalizationApproximately 3 months
Patient survey: Mean scores for correct responses for questions grouped by objectivesAt patient enrolmentObjectives: distribution, awareness, utility, utilization and knowledge
Patient survey: Mean total score for correct responsesAt patient enrolment
HCP survey: Proportion of HCPs who prescribe or administer abatacept in rheumatology centers who are aware of the PACDay 1
HCP survey: Proportion of HCPs' who have utilized the PAC, and the extent of its useDay 1
HCP survey: Levels of HCPs' knowledge and comprehension related to the important identified risks of infections and the need to screen for specific infection prior to initiating or administering abataceptDay 1
HCP survey: Mean total score for correct responsesDay 1
HCP survey: Mean scores for correct responses for questions grouped by objectivesDay 1Objectives: distribution, awareness, utility, utilization and knowledge
Patient survey: Proportion of patients treated with abatacept who are aware of the existence of the PACAt patient enrolment
Patient survey: Proportion of patients treated with abatacept who have received the PACAt patient enrolment
Patient survey: Proportion of patients who have utilised the PAC, and the extent of its useAt patient enrolment
Patient survey: Levels of patient knowledge and comprehension related to the important identified risks of allergic reactions associated with abatacept treatmentAt patient enrolment
Patient survey: Levels of patient knowledge and comprehension related to the important identified risks of associated with abatacept treatmentAt patient enrolment

Secondary

MeasureTime frameDescription
Major determinants of understanding the key messages contained in the abatacept IV, SC formulation PACs among patientsAt patient enrolmentDeterminants: Formulation of abatacept administered, country, age, gender, educational level, duration of arthritis, number of prescription medications, duration of therapy with abatacept, HCP guided or self-administration
Major determinants of implementation regarding the key messages contained in the abatacept IV, SC formulation PACs among patientsAt patient enrolmentDeterminants: Formulation of abatacept administered, country, age, gender, educational level, duration of arthritis, number of prescription medications, duration of therapy with abatacept, HCP guided or self-administration
Determinants of Health Care Professional (HCP) understanding, Implementation regarding key messages contained in the PAC based on data collected in the abatacept IV and SC formulation PACs among HCPsDay 1Determinants: type of HCP, role of the HCP, country, age and sex of the HCP, years in the specialty, number of HCPs in the unit, annual number of patients managed by the unit, number of patients for whom abatacept was prescribed in the previous 12 months, type of practice, type of institution (academic or non-academic), size of town
Retrospective chart review study (clinical outcome study): Proportion of patients with results of any test to screen for Tuberculosis (TB) prior to administration of therapy of abataceptUpto 8 years
Retrospective chart review study (clinical outcome study): Proportion of patients with results of any test to screen for viral hepatitis before administration of therapy with abataceptUpto 8 years
Retrospective chart review study (clinical outcome study): Mean time from infection (symptom onset) to receiving medical attentionUpto 8 years
Major determinants of patients knowledge of the key messages contained in the abatacept IV, Subcutaneous (SC) formulation PACs among patientsAt patient enrolmentDeterminants: Formulation of abatacept administered, country, age, gender, educational level, duration of arthritis, number of prescription medications, duration of therapy with abatacept, HCP guided or self-administration

Countries

France, Germany, Spain, Sweden, United Kingdom

Outcome results

None listed

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