?Effect of empowerment program on the perception of risk and health dimensions in patients with coronary heart disease

Clinical trial comparing the effectiveness of empowerment program on the perception of risk and health dimensions in two groups of patients with coronary heart disease

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201607254443N22

Enrollment

Registered

2017-06-30

Start date

2017-07-23

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

coronary artery disease. Atherosclerotic heart disease

Interventions

Intervention 1: In control group no intervention is conducted by researcher and patients receive routine cares of the ward. Intervention 2: In test group, intervention contains 3 workshop sessions in

In control group no intervention is conducted by researcher and patients receive routine cares of the ward.

In test group, intervention contains 3 workshop sessions in three consecutive days based on a 5-step MAGIC empowerment program is developed. Then, eight weekly telephone contacts in the 8 weeks to fol

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: adult 18-65 years; least ability to read and write; diagnosis of ischemic heart disease through diagnostic tests and physician; Ability to communicate; being in stable condition.

Exclusion criteria

Exclusion criteria: psychological problems; participate in the empowerment of similar.

Design outcomes

Primary

Measure	Time frame
Perception of risk. Timepoint: Before the the intervention, immediately after ending the intervention. Method of measurement: the perception of risk of heart disease scale(PRHDS).;Physical health. Timepoint: Before the the intervention, immediately after ending the intervention. Method of measurement: Seattle Angina Questionnaire(SAQ).;Life satisfaction. Timepoint: Before the the intervention, immediately after ending the intervention. Method of measurement: Life Engagement Test(LET).;Life orientation. Timepoint: Before the the intervention, immediately after ending the intervention. Method of measurement: Revised Life Orientation Test(LOT-R).;Optimism. Timepoint: Before the the intervention, immediately after ending the intervention. Method of measurement: Revised Life Orientation Test(LOT-R).	—

Measure

Time frame

Perception of risk. Timepoint: Before the the intervention, immediately after ending the intervention. Method of measurement: the perception of risk of heart disease scale(PRHDS).;Physical health. Timepoint: Before the the intervention, immediately after ending the intervention. Method of measurement: Seattle Angina Questionnaire(SAQ).;Life satisfaction. Timepoint: Before the the intervention, immediately after ending the intervention. Method of measurement: Life Engagement Test(LET).;Life orientation. Timepoint: Before the the intervention, immediately after ending the intervention. Method of measurement: Revised Life Orientation Test(LOT-R).;Optimism. Timepoint: Before the the intervention, immediately after ending the intervention. Method of measurement: Revised Life Orientation Test(LOT-R).

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactZakerimoghadam Masoumeh

Nursing midwifery faculty of Tehran university of medical sciences

zakerimo@sina.tums.ac.ir+98 21 6692 7171

Outcome results

None listed

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