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Improving medication adherence and satisfaction with pharmacist-provided services for heart failure patients using a risk management dashboard

A pragmatic improvement for medication adherence and patient satisfaction with pharmacist services with an interactive dashboard for heart failure with reduced ejection fraction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN13218468
Enrollment
70
Registered
2024-09-03
Start date
2025-02-01
Completion date
Unknown
Last updated
2024-11-12

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

Conditions

Heart failure Circulatory System

Interventions

Before conducting the education sessions, the pharmacists will review the patients’ medical records, including medications and laboratory data, using the portal system. This review is part of their st

Sponsors

National Taiwan University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with heart failure and a documented left ventricular ejection fraction (LVEF) <40%

Exclusion criteria

Exclusion criteria: 1. Patients unable to provide full informed consent 2. Patients unable to comply with study procedures 3. Patients unable to complete the required questionnaires in person on three occasions or return for follow-up visits 4. Patients who cannot understand or respond to the required questionnaires

Design outcomes

Primary

MeasureTime frame
Medication adherence will be assessed using the Morisky 8-item Medication Adherence Scale (MMAS-8) at baseline (T0), 3 months (T1), and 6 months (T2) after randomization.

Secondary

MeasureTime frame
1. Patient satisfaction with pharmacist services will be evaluated using the adapted Chinese version of the Patient Satisfaction with Pharmacist Services Questionnaire 2.0 (C-PSPSQ 2.0) at baseline (T0), 3 months (T1), and 6 months (T2) after randomization. 2. Facilitators and barriers to the implementation: To explore potential facilitators and barriers to the implementation of the dashboard, a subgroup of pharmacists and patients will complete the Acceptability of Intervention Measure, Intervention Appropriateness Measure, and Feasibility of Intervention Measure (AIM-IAM-FIM) questionnaire at 6 months (T2) after randomization.

Countries

Taiwan

Contacts

Public ContactWan-Tseng Hsu
wantsenghsu@ntu.edu.tw+886 (0)2 3366 8195

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026