the effect of classic chest massage therapy on pain in patients undergoing elective coronary artery bypass graft

the effect of classic chest massage therapy on pain following midsternotomy in the patients undergoing elective off-pump coronary artery bypass graft

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016010925913N1

Enrollment

Registered

2016-02-07

Start date

2016-03-05

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 Bypass Graft. Mechanical complication of coronary artery bypass and valve grafts

Interventions

Intervention 1: intervention group: received classic chest physiotherapy control group: no intervention. Intervention 2: Control group: in this study, the control group receive usual medications and c

Treatment - Other

intervention group: received classic chest physiotherapy control group: no intervention

Control group: in this study, the control group receive usual medications and cares Without any additional intervention.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: inclusion criteria:all patients undergoing elective coronary artery bypass graft in the Afshar cardiovascular research center of Yazd (50 patients); exclusion criteria: patients with chest pain caused by trauma; patients with a previous history of cardiac surgery; patients with chronic pain syndrome; patients with prolonged bleeding during hospital stay (more than 200 cc per hour); patients who had psychiatric disorders; patients who didn't want to continue participating in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: before intervention, the day 5 after intervention, one month after intervention. Method of measurement: using VAS questionnaire.	—

Secondary

Measure	Time frame
Quality of life. Timepoint: before intervention, the day 5 after intervention, one month after intervention. Method of measurement: using SF-36 questionnaire.;Anxiety. Timepoint: before intervention, the day 5 after intervention, one month after intervention. Method of measurement: using VAS questionnaire.;Hospital Stay. Timepoint: before discharge. Method of measurement: according to patient's medical record.	—

Measure

Time frame

Quality of life. Timepoint: before intervention, the day 5 after intervention, one month after intervention. Method of measurement: using SF-36 questionnaire.;Anxiety. Timepoint: before intervention, the day 5 after intervention, one month after intervention. Method of measurement: using VAS questionnaire.;Hospital Stay. Timepoint: before discharge. Method of measurement: according to patient's medical record.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Zolfaghari

Shahid Sadoughi Univesity of Medical Sciences and Health Services

mhmzolfaghari89@ssu.ac.ir, mhmzolfaghari89@gmail.com+98 353821308690

Outcome results

None listed

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