Skip to content

Evaluation a home based cardiac rehabilitation in myocardial infarction patient

Evaluation and designing a home-based cardiac rehabilitation in myocardial infarction patient based on health action process approach

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210509051235N1
Enrollment
165
Registered
2021-11-06
Start date
2021-10-23
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Myocardial infarction. ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction

Interventions

Intervention 1: Intervention group: This group receives a home-based cardiac rehabilitation program under the Android application based on the health action process approach for 8 weeks. Intervention

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with myocardial infarction with any diagnosis and treatment High risk people with a doctor's diagnosis Having a license from your doctor to participate in a cardiac rehabilitation program at home Having a mobile phone or tablet (Android) to receive the application (patient or a family member living with her) Willingness to participate in the study Have a minimum literacy

Exclusion criteria

Exclusion criteria: Mental dysfunction Musculoskeletal Disorder Lack of application and discontinue programs in the educational process

Design outcomes

Primary

MeasureTime frame
Physical activity score in IPAQ. Timepoint: Before,3 and 6 months after the intervention. Method of measurement: IPAQ Physical Activity Questionnaire.;Functional capacity score. Timepoint: Before and 6 months after the intervention. Method of measurement: 6 minute walk test.;Endothelial function of the heart. Timepoint: Before and 6 months after the intervention. Method of measurement: Flow mediated dilation.

Secondary

MeasureTime frame
Anxiety and depression score. Timepoint: Before and 6 after the intervention. Method of measurement: Standard Anxiety and Depression Inventory (HADS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Fallah

Esfahan University of Medical Sciences

fallah@mui.ac.ir+98 31 3577 3002

Outcome results

None listed

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