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Clinical Pharmacist-led Discharge Education Service in Acute Coronary Syndrome

Evaluation of a Clinical Pharmacist-led Discharge Education Service in Patients With Acute Coronary Syndrome: A Randomized Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05153707
Enrollment
177
Registered
2021-12-10
Start date
2021-01-15
Completion date
2022-06-15
Last updated
2023-03-16

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

Conditions

Acute Coronary Syndrome

Brief summary

To evaluate the impact of clinical pharmacist-led discharge education service in patients with acute coronary syndrome.

Detailed description

This prospective, randomized controlled study was conducted in patients with acute coronary syndrome in an cardiology service of tertiary training and research hospital. The clinical pharmacist, within the scope of the discharge education services, provided medication reconciliation, medication review, individually prepared patient medicine (pill) card, patient education (based on Health Belief Model by using written material and video, and verbally \[by using Teach back method especially for patients with low health literacy\]) and counseling (using behavior change techniques based on The Capability, Opportunity, and Motivation Behavior model). The control group received standard care.

Interventions

BEHAVIORALDischarge Education Program

medication reconciliation, medication review, individually prepared patient medicine (pill) card, patient education (based on Health Belief Model by using written material and video, and verbally \[by using Teach back method especially for patients with low health literacy\]) and counseling (using behavior change techniques based on The Capability, Opportunity, and Motivation Behavior model).

Sponsors

Marmara University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients admitted to the cardiology department due to acute coronary syndrome * Older than 18 years old

Exclusion criteria

* Patients who transferred to another ward * Patients with active malignancy * Patients with alzheimer and/or dementia diagnosis * Patient with \>%80 visual loss or deaf muteness reported at medical record

Design outcomes

Primary

MeasureTime frameDescription
30 days hospital re-admission for cardiac reasons30 daysProportion of patients readmitted to hospital for cardiac cause at 1 month

Secondary

MeasureTime frameDescription
Hospital re-admission for any reasons1 month, 3 months, 6 months, and 12 monthsProportion of patients readmitted to hospital for any cause through 1 year.
Emergency service visits1 month, 3 months, 6 months, and 12 monthsProportion of patients visited to emergency service through 1 year.
Major Adverse Cardiovascular Event1 month, 3 months, 6 months, and 12 monthsProportion of patients had major adverse cardiovascular event through 1 year.
Death for cardiac reason1 month, 3 months, 6 months, and 12 monthsProportion of patients died for cardiac cause through 1 year.
Hospital re-admission for cardiac reasons3 months, 6 months, and 12 monthsProportion of patients readmitted to hospital for cardiac cause through 1 year.
Medication Adherence1 month, 3 months, 6 months, and 12 monthsAdherence to Cardioprotective Medications (Clopidogrel, Statins, Beta-blockers, Angiotensin-converting enzyme (ACE) inhibitors/ Angiotensin receptor blocker (ARB) through 1 year assessed by Medication Adherence Report Scale (MARS). MARS assesses adherence through 5-item, summed to give a scale score ranging from 5 to 25, where higher scores indicate higher levels of reported adherence.
Quality of Life Measurement1 month, 3 months, 6 months, and 12 monthsChange in quality of life from baseline assessed with EuroQol questionnaire EQ-5D-3L through 1 year. (EQ-5D-3L) is a standardized scale for use as a measure of the quality of life. The EQ-5D-3L descriptive system comprises the following 5 dimensions (5D): mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has 3 levels (3L): no problems (1 point), some problems (2 points), extreme problems (3 points). This gives a total of 245 different health states, adding unconscious and dead.
Achieved Target Low-density Lipoprotein Value6 months, 12 monthsRate of patients achieved target low-density lipoprotein value
Death for any reason1 month, 3 months, 6 months, and 12 monthsProportion of patients dying for any cause through 1 year.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 8, 2026