NCT01127802

Brief Summary

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.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2010

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2010

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

May 20, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

May 21, 2010

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2011

Completed
Last Updated

May 21, 2010

Status Verified

May 1, 2010

Enrollment Period

1.2 years

First QC Date

May 20, 2010

Last Update Submit

May 20, 2010

Conditions

Coronary Artery Bypass Graft Surgery

Keywords

CABGfunctional statussymptoms distressquality of lifethe trajectory of functional statusthe changes of symptoms distressthe changes of quality of life

Eligibility Criteria

Age18 Years - 95 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients undergoing elective CABG surgery

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Chia-Hui Chen, Ph. D.

    National Taiwan University Hospital

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

May 20, 2010

First Posted

May 21, 2010

Study Start

January 1, 2010

Primary Completion

March 1, 2011

Study Completion

March 1, 2011

Last Updated

May 21, 2010

Record last verified: 2010-05