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Comparing the Effect of Face-to-Face and Mobile-Based Rehabilitation Programs on Treatment Adherence and Sexual Self-Efficacy of Patients After Acute Myocardial Infarction

Comparing the Effect of Face-to-Face and Mobile-Based Rehabilitation Programs on Treatment Adherence and Sexual Self-Efficacy of Patients After Acute Myocardial Infarction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250105064284N1
Enrollment
120
Registered
2025-05-28
Start date
2025-06-04
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Rehabilitation after Acute Myocardial Infarction. Other acute ischemic heart diseases

Interventions

Intervention 1: Intervention group: First intervention group (face-to-face intervention group): Patients in this group will undergo in-person cardiac rehabilitation training for two months, during eig

Sponsors

Ilam University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Definite Diagnosis of Acute Myocardial Infarction Willingness to Participate in the Study Having Minimum Literacy Being Between 18 and 65 Years Of Age Residing in Ilam City Completing the Informed Consent Form to Participate in the Study Being Married and Living with a Spouse Sufficient Physical Ability (Exercise Test and Cardiologist Prescription) to Participate in the Study No previous Percutaneous Coronary Intervention No Previous Coronary Artery Bypass Surgery Access to a Mobile Phone Knowing How to Use a Mobile Phone or Having Access to Someone Who Can Help the Patient Use it

Exclusion criteria

Exclusion criteria: Incomplete or Non-Completion of Questionnaires Withdrawal From the Study Insufficient Mental and Physical Ability to Participate in the Study A History of Neurological and Psychiatric Diseases, Alzheimer's Disease, or Debilitating Physical Diseases, Including Stroke Hospitalization or Death During the Study Death of Spouse During the Study Failure to Participate in More Than Two Sessions of the Educational Program

Design outcomes

Primary

MeasureTime frame
Treatment Adherence. Timepoint: Before Entering the Intervention - One Month after Entering the Intervention - Two Months after Entering the Intervention - One Month after the End of the Intervention. Method of measurement: Treatment Adherence Questionnaire (Modanloo, 2013).;Sexual Self-Efficacy. Timepoint: Before Entering the Intervention - One Month after Entering the Intervention - Two Months after Entering the Intervention - One Month after the End of the Intervention. Method of measurement: Vaziri and Lotfi Sexual Self-Efficacy Questionnaire (2013).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNegin Gholami

Ilam University of Medical Sciences

negingholami124@yahoo.com+98 84 3222 7134

Outcome results

None listed

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