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FrailtyNCT06343168

Prevalence of Frailty and Associated Factors in Coronary Artery Bypass Patients

An observational study of Frailty, run by Uşak University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Frailty
What is being tested?
prevalence of frailty
How many people
96 participants
Where
1 siteTurkey (Türkiye)
Study dates
18 Feb 2021to 18 Feb 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

Study population: coronary artery bypass grafting patients

Who may be able to join

  • 18 years and older
  • planned CABG surgery
  • volunteer to participate in the study

Who cannot join

  • limb amputations
  • stroke-related sequela
  • hearing problems
  • clinically unstable

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Usak University

    Uşak, Center, 64200

Other trials in Turkey (Türkiye)

About this study

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

Conditions
Frailty
Being tested
prevalence of frailty
Medical subject headings
Frailty

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • prevalence of frailtyOther

    determine the prevalence of frailty

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Prevalence of frailty

    Modified Fried Frailty Index

    Measured: Preoperative

Secondary outcomes (4)
  1. Activities of Daily Living

    Barthel Activities of Daily Living Index

    Measured: Preoperative

  2. Nutritional Assessment

    Mini Nutritional Assessment Test-Short Form

    Measured: Preoperative

  3. Comorbidity

    Charlson Comorbidity Index

    Measured: Preoperative

  4. Cognitive Assessment

    Montreal Cognitive Assessment

    Measured: Preoperative

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Apr 2024
  2. Study start18 Feb 2021
  3. Primary completion18 Feb 2022
  4. Study completion18 Feb 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
96 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06343168
Sponsor's protocol ID
frailty
Status last verified
Mar 2024
First submitted
26 Mar 2024
Last updated
2 Apr 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Frailty, run by Uşak University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Prevalence of frailty (time frame: Preoperative). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Apr 2024.

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