The effect of positive psychology-based audio messages on patients with acute coronary syndrome

The effect of positive psychology-based audio messages on psychological variables in patients with acute coronary syndrome

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017092532764N4

Enrollment

Registered

2017-11-05

Start date

2017-11-22

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 coronary syndrome. Condition 2: acute coronary syndrome. Condition 3: acute coronary syndrome. Condition 4: acute coronary syndrome. Condition 5: acute coronary syndrome. Angina pectoris acute myocardial infarction Subsequent myocardial infarction Certain current complications following acute myocardial infarction Other acute ischaemic heart diseases

Interventions

Intervention 1: Intervention group: they will receive audio file of positive psychological messages with topics of morning optimism, short term and temporal hospitalization, positive perception of CCU

Intervention group: they will receive audio file of positive psychological messages with topics of morning optimism, short term and temporal hospitalization, positive perception of CCU hospitalization

Control group: They will receive audio file of self-care messages with the topics related to getting acquainted with the cardiac care unit, the cardiovascular system, the risk factors of coronary arte

Eligibility

Sex/Gender

All

Age

30 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: confirmation of Acute Coronary Syndrome by Cardiologist; no history of hospitalization in the cardiac care unit; willingness to participate in the study; ability to understand conversation in Persian language; age of 30 to 75 years; no use of psychological treatment; having no hearing problems Exclusion criteria: failure to co-operate with the patient; patient's death during the study; complications of life threatening complications

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Anxiety. Timepoint: before the intervention, after discharge from the hospital, one week after the intervention and six weeks after the intervention. Method of measurement: Hospital Anxiety And Depression Scale.;Depression. Timepoint: before the intervention, after discharge from the hospital, one week after the intervention and six weeks after the intervention. Method of measurement: Hospital Anxiety And Depression Scale.;Hope. Timepoint: before the intervention, after discharge from the hospital, one week after the intervention and six weeks after the intervention. Method of measurement: Hope Questionary.;Optimism. Timepoint: before the intervention, after discharge from the hospital, one week after the intervention and six weeks after the intervention. Method of measurement: Life Orientation Test-Reviseved.;Positive affect. Timepoint: before the intervention, after discharge from the hospital, one week after the intervention and six weeks after the intervention. Method of measurement: Positive and Negative Affect Scale (PANAS).	—

Measure

Time frame

Anxiety. Timepoint: before the intervention, after discharge from the hospital, one week after the intervention and six weeks after the intervention. Method of measurement: Hospital Anxiety And Depression Scale.;Depression. Timepoint: before the intervention, after discharge from the hospital, one week after the intervention and six weeks after the intervention. Method of measurement: Hospital Anxiety And Depression Scale.;Hope. Timepoint: before the intervention, after discharge from the hospital, one week after the intervention and six weeks after the intervention. Method of measurement: Hope Questionary.;Optimism. Timepoint: before the intervention, after discharge from the hospital, one week after the intervention and six weeks after the intervention. Method of measurement: Life Orientation Test-Reviseved.;Positive affect. Timepoint: before the intervention, after discharge from the hospital, one week after the intervention and six weeks after the intervention. Method of measurement: Positive and Negative Affect Scale (PANAS).

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Hadadzadeh

Shahrekord University of Medical Sciences and Health Service

sarahadad1363@gmail.com+98 381330061

Outcome results

None listed

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