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Developing a Family-centered Health Program and Comparing its Effectiveness with Cardiac Rehabilitation Program on Biological and Psychological Components in Individuals with Coronary Heart Disease

Developing a Family-centered Health Program and Comparing its Effectiveness with Cardiac Rehabilitation Program on Biological and Psychological Components in Individuals with Coronary Heart Disease

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210307050608N1
Enrollment
120
Registered
2022-03-14
Start date
2022-01-20
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Coronary Heart Disease. Atherosclerotic heart disease of native coronary artery with angina pectoris

Interventions

Intervention 1: Intervention group: Drug treatments and 8 sessions of Family-centered Health Program receive 2 to 2.5 hours and one a week. Intervention 2: Intervention group: Drug treatments and 8 se

Sponsors

Faculty of Psychology and Educational Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: The criteria for admitting the subjects in this study include:- Diagnosis of coronary heart disease patients. - Education level of junior high school or above - 40 to 65 years of age - No history of hospitalization in psychiatric hospitals - History of Percutaneous Coronary Intervention - Being married - Willingness to participate in the study

Exclusion criteria

Exclusion criteria: The exclusion criteria for the experimental group include Reluctance to continue attending the intervention sessions - Patients with acute myocardial infarction or acute coronary syndrome - History of Coronary Artery Bypass Grafting (CABG) - History of inflammatory diseases such as collagen vascular disease, avascular necrosis, and chronic infectious diseases - Primary Percutaneous Coronary Intervention

Design outcomes

Primary

MeasureTime frame
The effectiveness of Family-centered health program Blood Pressure. Timepoint: Before an intervention, immediately after the intervention, 3 months after the end of intervention. Method of measurement: In this study, patients with coronary heart disease (CHD) will be identified by cardiologists.;The effectiveness of Family-centered health program in Body Mass Index. Timepoint: Before an intervention, immediately after the intervention, 3 months after the end of intervention. Method of measurement: BMI is weight in kilograms divided by height in meters squared. Weight will be measured using a digital scale with 100 gram accuracy, and height will be measured accurately using a non-stretching tape measure with 0.5 accuracy.;The effectiveness of Family-centered health program in Awareness, attitudes, and adherence to self-care behaviors. Timepoint: Before an intervention, immediately after the intervention, 3 months after the end of intervention. Method of measurement: In this study, self-care will be determined based on the subject's score on the Health Behavior Scale (Conn et al., 1991).;The effectiveness of Family-centered health program model in Health-related quality of life. Timepoint: Before an intervention, immediately after the intervention, 3 months after the end of intervention. Method of measurement: In this study, health-related quality of life will be determined based on the subject's score in the Health-Related Quality of Life Scale.;The effectiveness of Family-centered health program model on depression, Anxiety and Stress. Timepoint: Before an intervention, immediately after the intervention, 3 months after the end of intervention. Method of measurement: In this study, depression, Anxiety and Stress level will be determined based on t The Depression, Anxiety and Stress Scale - 21 Items.

Secondary

MeasureTime frame
Heart Rate. Timepoint: Before an intervention, immediately after the intervention, 3 months after the end of intervention. Method of measurement: In this study, heart rate will be determined by heart rate monitor device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNegin Dorri

University of Tehran Kish International Campus Branch

negin.dorri@ut.ac.ir+98 21 2254 0944

Outcome results

None listed

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