comparative effect of preoperative resistance and aerobic training in pre frail to moderately frail patients for improving quality of recovery in post coronary artery bypass grafting surgery patients

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220902055851N1

Enrollment

Registered

2022-10-17

Start date

2022-06-04

Completion date

Unknown

Last updated

2022-11-21

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

Conditions

CABG (coronary artery bypass grafting surgery). Cardiac rehabilitation

Interventions

Intervention 1: Intervention group 1: After giving participants the baseline treatment. Group A recieved aerobic training included walking for 10-15 minutes and stepping 8-12 repetitions. Intervention

Eligibility

Sex/Gender

All

Age

45 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age: 4o -65 years Both male and female Patient with double and triple vessel coronary artery disease Patients who were mildly to moderately frail and had a Clinical Frailty Scale of 4-6 before surgery at the hospital setting

Exclusion criteria

Exclusion criteria: Patient with unstable or recently unstable cardiac syndrome Prehabilitation is contraindicated in cases where a patient cannot follow study protocols due to cognitive impairment Patients who are severely frail (CSF 7-9) A lack of consistency in attending prehabilitation treatments

Design outcomes

Primary

Measure	Time frame
The primary outcome was Quality of recovery. Timepoint: 3 timepoints including Baseline, preoperative 3rd week after treatment and postoperative before discharge. Method of measurement: 15- item Quality of recovery was utilized to assess pain.	—

Secondary

Measure	Time frame
The secondary outcome was frailty. Timepoint: 3 timepoints including Baseline, preoperative 3rd week after treatment and postoperative before discharge. Method of measurement: Clinical Frailty Scale was used to assess frailty. The CFS scale consist of 9 points, which range from non-frail that scores 1–3, vulnerable/pre-frail that has scoring of 4 and frailty scores from 5–9.;Another secondary outcome was disability free survival. Timepoint: 2 timepoints including baseline and postoperative one month after discharge. Method of measurement: WHO Disability Assessment Schedule 2.o score was used to monitor changes in disability free survival. Disability scores ranges from 0-4%, 5-24%, 25-49%, 50-95%, 96-100% for none, mild moderate, severe and complete disability respectively.	—

Measure

Time frame

The secondary outcome was frailty. Timepoint: 3 timepoints including Baseline, preoperative 3rd week after treatment and postoperative before discharge. Method of measurement: Clinical Frailty Scale was used to assess frailty. The CFS scale consist of 9 points, which range from non-frail that scores 1–3, vulnerable/pre-frail that has scoring of 4 and frailty scores from 5–9.;Another secondary outcome was disability free survival. Timepoint: 2 timepoints including baseline and postoperative one month after discharge. Method of measurement: WHO Disability Assessment Schedule 2.o score was used to monitor changes in disability free survival. Disability scores ranges from 0-4%, 5-24%, 25-49%, 50-95%, 96-100% for none, mild moderate, severe and complete disability respectively.

—

Countries

Pakistan

Contacts

Public ContactDr. Komal Tariq; PT

Faisal Institute Of Health Sciences

fihsfsd@outlook.com+92 41 8536999

Outcome results

None listed

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