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Evaluation of retraining in acute coronary syndrome

Investigating the effect of self-care training in a retrospective method on treatment compliance and post-discharge outcomes in patients with acute coronary syndrome.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241210064019N1
Enrollment
146
Registered
2025-01-02
Start date
2024-12-22
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Acute coronary syndrome. ??? ?? ????? ??????? ?????? ?? ????? ???? ????? ? ????????? ?????? ??? ?? ????????? ???? ??? ???? (????? ??? ???? ???? ?? ???? ???) ??? ????? ???? ??? ??????????? ????? ????? ??? ?????? (ACS) (????? STEMI? NSTEMI ?? ????? ????????) ???? ???? ????.????????

Interventions

Intervention 1: In the first step, which is at the time of hospitalization of the patients, after completing the questionnaires, face-to-face training and broadcasting an educational video about the c

Sponsors

Hormozgan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed with acute coronary syndrome with non-ST-segment elevation ACS (NSTE-ACS) Being a resident of Bandar Abbas city In terms of physical and mental conditions, have the ability to participate in training sessions. Able to read and write. Interested and satisfied to participate in this research. Age 20 to 60 years

Exclusion criteria

Exclusion criteria: Patients with other patterns of acute coronary syndrome Having other diseases (kidney, tumors, stroke) Unwillingness to cooperate and participate in research Participation in another clinical trial study Participant who missed two sessions was excluded from the study

Design outcomes

Primary

MeasureTime frame
"adherence to treatment". Timepoint: On the first day of hospitalization, before discharge, 30, 60, 90 days after the first training. Method of measurement: Medanlo treatment compliance questionnaire.;"fatigue". Timepoint: On the first day of hospitalization, before discharge, 30, 60, 90 days after the first training. Method of measurement: Fatigue checklist.;"pain". Timepoint: On the first day of hospitalization, before discharge, 30, 60, 90 days after the first training. Method of measurement: Numerical pain rating scale.;"rehospitalization". Timepoint: 30-60-90 days after discharge and initial training from the hospital. Method of measurement: " ?????? ????? " ?? " ???? ? ???? ?? ????? ".

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Mohseni

Hormozgan University of Medical Sciences

hossein136447@gmail.com+98 76 3368 1873

Outcome results

None listed

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