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Changes of Functional Status, Symptoms Distress and Quality of Life in Patients Undergoing Coronary Artery Bypass Graft (CABG) Surgery

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National Taiwan University

Status

Unknown

Conditions

Coronary Artery Bypass Graft Surgery

Study type

Observational

Funder types

Other

Identifiers

NCT01127802
201003017R

Details and patient eligibility

About

The purpose of this study is to explore the changes of functional status, symptoms distress and quality of life in patients undergoing coronary artery bypass graft (CABG) surgery.

Full description

This is an observational cohort study. The participants will be inpatients undergoing elective CABG surgery at one tertiary medical center. Functional status (including activity of daily living, cognitive and nutritional status), symptom distress, and quality of life will be measured at multiple points: pre-surgery, day 1 to 7 post-surgery, before discharge, and 2-4 weeks after discharge. Structured questionnaire will be used to collect demographic and medical characteristics. The Barthel Index, hand-held dynamometer, 6-minute walking test, Mini-Nutritional Assessment (MNA), Mini-Mental State Examination (MMSE), Confusion Assessment Method (CAM), Symptoms Distress Scale, and Short-Form-36 Health Survey (SF-36) will be used to collect functional data and compared for changes. The trajectory of functional status, symptoms distress, and quality of life will be further analyzed. The findings will add to the literature by raising the awareness on changes of functional status, symptoms distress, and quality of life for patients undergoing elective CABG so targeted and timely intervention could be developed and planned.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • receive elective coronary artery bypass surgery
  • able to communicate in Chinese and Taiwanese
  • walk independently or use walker
  • length of stay is over 7 days

Exclusion criteria

  • unable to walk
  • mechanical ventilation
  • neural or muscle disease to influence ambulation(ex: Parkinson Disease)
  • asthma
  • severe psychotic disorder that prevents patient from participating in test

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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