The effect of telephone follow-up and educational programs on the quality of life and satisfaction in acute coronary syndrome patient

The effect of telephone follow-up and educational program on the quality of life and patient satisfaction in three groups: telephone follow-up, present education and control

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201507252165N1

Enrollment

Registered

2015-09-01

Start date

2013-03-20

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Condition 1: Acute myocard infarction. Condition 2: Unstable angina. Incl.: myocardial infarction specified as acute or with a stated duration of 4 weeks (28 days) or less from onset Excl.: certain current complications following acute myocardial infarction (I23.-) myocardial infarction: old (I25.2) Angina: crescendo de novo effort worsening effort Intermediate coronary syndrome Preinfarction syndrome

Interventions

Intervention 1: Telephone follow-up group: receiving 10 telephone contacts after discharge and 3 educational session about control of heart disease during their hospitalized. Intervention 2: Present e

receiving 3 educational session about control of heart disease. Intervention 3: Control group

no receiving intervention.

Lifestyle

Telephone follow-up group: receiving 10 telephone contacts after discharge and 3 educational session about control of heart disease during their hospitalized

Present educational group

receiving 3 educational session about control of heart disease

Control group

no receiving intervention

Eligibility

Sex/Gender

All

Age

25 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:diagnosis of Acute Coronary Syndrome; being 25-70- years old; hospitalized in department of heart or CCU; signing the informed consent form; the patient,s or relative ability to write and read; the patient s access to telephone; no hearing or speaking problem; speaking Persian, lori, laki; no pain; willingness to review the educational program; permission to make telephone calls after discharge; willingness to visit 2month after discharge; not suffering from mental disorder; exclusion criteria: no access to the patient after 2month; the patients unwilling to continue the study; the patient death; no more access to the patient; Change of telephone number and no response to telephone follow-up.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Quality of life. Timepoint: Before and 2 month after intervention. Method of measurement: MAC NEW Questionnaries.;Patient Satisfaction. Timepoint: Before and 2 month after intervention. Method of measurement: Satisfaction Questionnarie.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Tahereh Toulabi

Lorestan University of Medical Science

tolabi.t@lums.ac.ir+98 66 3620 0165

Outcome results

None listed

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