The Effect of Cognitive-Behavioral Couple Therapy on Patients with Coronary Artery Bypass

The Efficiency of Cognitive-Behavioral Couple Therapy on Quality of Life, Depression, Anxiety and Stress in Patients with Coronary Artery Bypass

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200725048202N1

Enrollment

Registered

2020-10-18

Start date

2020-10-18

Completion date

Unknown

Last updated

2020-11-09

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

Conditions

Coronary artery bypass.

Interventions

Intervention 1: Intervention group: The group will receive 10 sessions of cognitive-behavioral couple therapy training. Intervention 2: Control group: Members of this group will not receive any traini

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with coronary artery bypass grafting surgery Being married More than a year has passed since their marriage Patients have undergone coronary artery bypass graft surgery in the past year

Exclusion criteria

Exclusion criteria: Patients over 65 years Depression, anxiety, stress and poor quality of life are caused by illness Patients who do not want to participate in sessions in pairs Patients with myocardial infarction Be addicted to alcohol and drugs Participate in other psychological training sessions in parallel EF (Ejection Fraction) is under 40%

Design outcomes

Primary

Measure	Time frame
Quality of life score in Varosherbon Questionnaire. Timepoint: Measurement of quality of life at the beginning of the study (pre-test), 30 days, 62 days after the intervention (post-test). Method of measurement: Varosherbon Quality of Life Questionnaire.;Depression score in Lovibond and Lovibond Scale. Timepoint: Measurement of depression at the beginning of the study (pre-test), 30 days, 62 days after the intervention (post-test). Method of measurement: Lovibond and Lovibond Depression, Anxiety and Stress Scale.;Anxiety score in Lovibond and Lovibond Scale. Timepoint: Measurement of anxiety at the beginning of the study (pre-test), 30 days, 62 days after the intervention (post-test). Method of measurement: Lovibond and Lovibond Depression, Anxiety and Stress Scale.;Stress score in Lovibond and Lovibond Scale. Timepoint: Measurement of stress at the beginning of the study (pre-test), 30 days, 62 days after the intervention (post-test). Method of measurement: Lovibond and Lovibond Depression, Anxiety and Stress Scale.	—

Measure

Time frame

Quality of life score in Varosherbon Questionnaire. Timepoint: Measurement of quality of life at the beginning of the study (pre-test), 30 days, 62 days after the intervention (post-test). Method of measurement: Varosherbon Quality of Life Questionnaire.;Depression score in Lovibond and Lovibond Scale. Timepoint: Measurement of depression at the beginning of the study (pre-test), 30 days, 62 days after the intervention (post-test). Method of measurement: Lovibond and Lovibond Depression, Anxiety and Stress Scale.;Anxiety score in Lovibond and Lovibond Scale. Timepoint: Measurement of anxiety at the beginning of the study (pre-test), 30 days, 62 days after the intervention (post-test). Method of measurement: Lovibond and Lovibond Depression, Anxiety and Stress Scale.;Stress score in Lovibond and Lovibond Scale. Timepoint: Measurement of stress at the beginning of the study (pre-test), 30 days, 62 days after the intervention (post-test). Method of measurement: Lovibond and Lovibond Depression, Anxiety and Stress Scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Abbaszadeh

Islamic Azad University

m.abbaszadeh90@gmail.com+98 41 3386 2656

Outcome results

None listed

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