Assessment of Medication Adherence in Ccu Admitted Patients
1 other identifier
observational
250
1 country
2
Brief Summary
This study aims to assess medication adherence and the appropriateness of prescribed medications among patients admitted to the Coronary Care Unit (CCU). The study will use the Medication Appropriateness Index (MAI) to evaluate the suitability of prescribed medications and the Beliefs about Medicines Questionnaire (BMQ) to assess patients' beliefs and perceptions regarding their medications. Understanding medication adherence and related beliefs may help identify factors associated with inappropriate medication use and non-adherence in hospitalized cardiac patients. The findings of this study may contribute to improving medication management and patient care in the CCU setting.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2026
Shorter than P25 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2026
CompletedFirst Submitted
Initial submission to the registry
March 3, 2026
CompletedFirst Posted
Study publicly available on registry
March 31, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
March 31, 2026
March 1, 2026
5 months
March 3, 2026
March 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Medication adherence (BMQ)
Medication adherence will be assessed using the Brief Medication Questionnaire (BMQ), a validated tool that evaluates medication-taking behavior and barriers to adherence.
During CCU admission after clinical stabilization (assessed up to 5 days)
Medication appropriateness measured by Medication Appropriateness Index (MAI)
Medication appropriateness will be assessed using the Medication Appropriateness Index (MAI). The MAI score ranges from 0 to 12, where lower scores indicate better medication adherence and higher scores indicate poorer adherence.
During CCU admission after clinical stabilization (assessed up to 5 days)
Study Arms (1)
CCU HF and AF Patients
Adult patients aged 18 years or older diagnosed with atrial fibrillation or heart failure and discharged from the coronary care unit.
Interventions
This is an observational study with no active intervention.
Eligibility Criteria
Adult patients aged 18 years or older diagnosed with atrial fibrillation or heart failure who are admitted to the coronary care unit. Participants will be clinically stable at the time of assessment and able to provide informed consent.
You may qualify if:
- Adult patients aged 18 years or older
- Diagnosed with atrial fibrillation or heart failure
- Admitted to the coronary care unit
- Clinically stable at the time of interview
- Able to provide informed consent
You may not qualify if:
- Significant cognitive impairment
- Communication difficulties preventing interview
- Diagnosed psychiatric disorder interfering with participation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Al-Nasiriyah Heart Center
Nasiriyah, Thi Qar, Iraq
Al-Nasiriyah Teaching Hospital
Nasiriyah, Thi Qar, Iraq
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 3, 2026
First Posted
March 31, 2026
Study Start
March 1, 2026
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Last Updated
March 31, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to the nature of the study and the absence of a formal data sharing plan.