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Assessing the impact of planned behavior theory oriented intervention on drug adherence

Assessing the impact of planned behavior theory oriented intervention on drug adherence in patients undergoing coronary angioplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220814055689N1
Enrollment
88
Registered
2023-09-03
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Coronary Angioplasty. Presence of coronary angioplasty implant and graft

Interventions

Intervention 1: Intervention group: At the patient s first visit to the clinic, after registering their information in the demographic questionnaire, the level and proportion of medication adherence a

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: History of coronary angioplasty Positive behavioral intention to take medicine Absence of underlying chronic non-cardiac disease that affects the quality of life. Physical and cognitive ability and independence of medication use. Age requirement:18 to 75 years Literacy for reading and writing

Exclusion criteria

Exclusion criteria: Lack of mental health Diseases or surgeries that require not taking anti-platelet drugs.

Design outcomes

Primary

MeasureTime frame
The rate of drug adherence after coronary angioplasty. Timepoint: Prior to intervention, 30 days after intervention, and 60 days after intervention. Method of measurement: The determination of medication adherence level using the Morisky Medication Adherence Scale,.;The ratio of drug adherence after coronary angioplasty. Timepoint: Prior to intervention, 30 days after intervention, and 60 days after intervention. Method of measurement: measuring the ratio of medication adherence using the Brazilian Global Evaluation of Medication Adherence (GEMA).

Secondary

MeasureTime frame
The rate of readmission of patients. Timepoint: 60 days after intervention. Method of measurement: Patient information questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDR.Elham Navab

Tehran University of Medical Sciences

elhamnavab2@gmail.com+98 21 6105 4000

Outcome results

None listed

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