- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06343168
Prevalence of Frailty and Associated Factors in Coronary Artery Bypass Patients
March 26, 2024 updated by: Uşak University
This study aimed to determine the prevalence of and factors affecting frailty in patients with coronary artery bypass graft.
The main question it aims to answer are:
What are the prevalence of and factors affecting frailty in patients with coronary artery bypass graft Type of study: descriptive cross-sectional study Participant population: coronary artery bypass grafting patients
Study Overview
Study Type
Observational
Enrollment (Actual)
96
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Center
-
Usak, Center, Turkey, 64200
- Uşak University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
coronary artery bypass grafting patients
Description
Inclusion Criteria:
- 18 years and older
- planned CABG surgery
- volunteer to participate in the study
Exclusion Criteria:
- limb amputations
- stroke-related sequela
- hearing problems
- clinically unstable
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of frailty
Time Frame: Preoperative
|
Modified Fried Frailty Index
|
Preoperative
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Activities of Daily Living
Time Frame: Preoperative
|
Barthel Activities of Daily Living Index
|
Preoperative
|
|
Nutritional Assessment
Time Frame: Preoperative
|
Mini Nutritional Assessment Test-Short Form
|
Preoperative
|
|
Comorbidity
Time Frame: Preoperative
|
Charlson Comorbidity Index
|
Preoperative
|
|
Cognitive Assessment
Time Frame: Preoperative
|
Montreal Cognitive Assessment
|
Preoperative
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 18, 2021
Primary Completion (Actual)
February 18, 2022
Study Completion (Actual)
February 18, 2022
Study Registration Dates
First Submitted
March 26, 2024
First Submitted That Met QC Criteria
March 26, 2024
First Posted (Actual)
April 2, 2024
Study Record Updates
Last Update Posted (Actual)
April 2, 2024
Last Update Submitted That Met QC Criteria
March 26, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FRAILTY
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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