Effect of progressive muscle relaxation on the coronary artery bypass graft patients

Effect of progressive muscle relaxation on the different outcomes of coronary artery bypass graft patients: A randomized controlled clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20160901029640N1

Enrollment

Registered

2018-03-15

Start date

2018-02-05

Completion date

Unknown

Last updated

2018-03-26

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

Conditions

Coronary artery disease. Ischaemic heart diseases

Interventions

Intervention 1: Intervention group: At the first, progressive muscle relaxation technique is taught to the patients, and then, the learning of patient will be assured by the researcher. During the po

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: age 18-75 years Performing the heart surgery for the first time left ventricular ejection fraction more than 30% patient's complete alertness

Exclusion criteria

Exclusion criteria: Patient's unwillingness to participate in the study Emergency heart surgery Confirmed psychological problems Prohibition of repeated muscle contraction and expansion Exacerbation of the patient's condition

Design outcomes

Primary

Measure	Time frame
Quality of life. Timepoint: Pre-intervention, one and Two months after intervention. Method of measurement: SF-36 Quality of life questionnaire.;Perceived stress. Timepoint: Pre-intervention, one, and Two months after intervention. Method of measurement: Cohen,s perceived stress questionnaire.;Self-esteem. Timepoint: Pre-intervention, one, and Two months after intervention. Method of measurement: Coper esmeet self-esteem questionnaire.;Trait and state anxiety. Timepoint: Pre-intervention, one , and two months after intervention. Method of measurement: Spielberg trait and estate questionnaire.;Sleep quality. Timepoint: Pre-intervention, one, and two months after intervention. Method of measurement: Sleep quality questionnaire.;Vital signs (Pulse and respiratory rate, systolic and diastolic pressure, temperature, and pain). Timepoint: Pre-intervention, one, and two months after intervention. Method of measurement: Checklist for recording mentioned vital signs.	—

Measure

Time frame

Quality of life. Timepoint: Pre-intervention, one and Two months after intervention. Method of measurement: SF-36 Quality of life questionnaire.;Perceived stress. Timepoint: Pre-intervention, one, and Two months after intervention. Method of measurement: Cohen,s perceived stress questionnaire.;Self-esteem. Timepoint: Pre-intervention, one, and Two months after intervention. Method of measurement: Coper esmeet self-esteem questionnaire.;Trait and state anxiety. Timepoint: Pre-intervention, one , and two months after intervention. Method of measurement: Spielberg trait and estate questionnaire.;Sleep quality. Timepoint: Pre-intervention, one, and two months after intervention. Method of measurement: Sleep quality questionnaire.;Vital signs (Pulse and respiratory rate, systolic and diastolic pressure, temperature, and pain). Timepoint: Pre-intervention, one, and two months after intervention. Method of measurement: Checklist for recording mentioned vital signs.

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Secondary

Measure	Time frame
Arterial Blood Oxygen saturation. Timepoint: Pre-intervention, one, and two months after intervention. Method of measurement: Checklist.;Daily activity living. Timepoint: Pre-intervention, one, and two months after intervention. Method of measurement: Daily activity living questionnaire.;Psychological distress. Timepoint: Pre-intervention, one, and two months after intervention. Method of measurement: Psychological distress questionnaire.	—

Measure

Time frame

Arterial Blood Oxygen saturation. Timepoint: Pre-intervention, one, and two months after intervention. Method of measurement: Checklist.;Daily activity living. Timepoint: Pre-intervention, one, and two months after intervention. Method of measurement: Daily activity living questionnaire.;Psychological distress. Timepoint: Pre-intervention, one, and two months after intervention. Method of measurement: Psychological distress questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Amir vahedian-azimi

Bagheiat-allah University of Medical Sciences

amirvahedian63@gmail.com+98 21 8248 3505

Outcome results

None listed

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