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

Not Applicable
Recruiting
Conditions
Coronary artery disease.
Ischaemic heart diseases
Registration Number
IRCT20160901029640N1
Lead Sponsor
Bagheiat-allah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
90
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

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

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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.
Secondary Outcome Measures
NameTimeMethod
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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