Actively Recruiting

Age: 65Years +
All Genders
ID07633483

Assessment of the Relationship Between Preoperative Anxiety Level and Frailty Score in Elderly Patients Scheduled for Elective Hip Arthroplasty

Led by Başakşehir Çam & Sakura City Hospital · Updated on 2026-06-08

142

Participants Needed

1

Research Sites

2 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the relationship between preoperative anxiety levels and frailty scores in elderly patients aged 65 years and older who are scheduled for elective hip replacement surgery. Frailty is a condition marked by decreased physical reserve across multiple body systems, making individuals more vulnerable to stress. Anxiety is a common psychiatric condition that may impact surgical outcomes, especially in older patients. This prospective observational study seeks to better understand how these factors interact before surgery. The study involves assessing frailty using the FRAIL Scale, which measures fatigue, resistance, ambulation, illness, and weight loss, and anxiety using the Hamilton Anxiety Rating Scale (HAM-A). Eligible participants will be evaluated at three visits: the day of hospital admission for routine preoperative assessments, 24 hours before surgery for anxiety and frailty scoring plus sociodemographic data collection, and the day of discharge for postoperative monitoring. Participants are grouped based on their frailty scores into robust, pre-frail, and frail categories. During the study, researchers will collect medical history, physical status, hemodynamic and laboratory data, and record hospital stay length and ICU admission rates. The main goal is to examine the association between frailty and anxiety levels before surgery. Secondary measurements include the prevalence of frailty and anxiety, and their correlations with hospital stay duration, ICU admissions, and in-hospital mortality. Data will be securely stored and analyzed to identify relevant relationships over the course of the hospitalization, which may last up to two weeks.

CONDITIONS

Brief Title

The Relationship Between Preoperative Anxiety Level and Frailty Score in Elderly Patients Scheduled for Elective Hip Arthroplasty: A Prospective Observational Study

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients of both sexes aged 65 years and older
  • Patients with ASA physical status classification I, II, or III scheduled for elective hip arthroplasty
  • Patients who voluntarily agree to participate in the study
  • Patients with intact orientation and sufficient cooperation for assessment
Not Eligible

You will not qualify if you...

  • Patients with ASA physical status classification IV or V
  • Patients who refuse to participate in the study
  • Patients with impaired orientation or insufficient cooperation for assessment
  • Patients scheduled for emergency surgery
  • Patients to be operated during an active intensive care unit admission

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) on the day of admission

Diagnostic Evaluation

Duration - 2 days (from hospital admission to 24 hours before surgery)

Participants undergo routine preoperative assessments including anesthesia evaluation, medical history, hemodynamic and laboratory measurements, and assessments of frailty and anxiety levels.

2 visits (in-person): Day of Admission and 24 hours before surgery

Monitoring

Duration - From hospital admission to discharge, up to 2 weeks

Participants are observed during their hospital stay with hemodynamic monitoring and documentation of hospital length of stay and intensive care unit admissions if applicable.

1 visit (in-person) on day of discharge

Trial Site Locations

Total: 1 location

1

Basaksehir Çam Ve Sakura City Hospital, İstanbul, Türkiye

Istanbul, Istanbul, Turkey (Türkiye), 34480

Actively Recruiting

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Research Team

M

Muzaffer GENCER

M

Murat Yasin MERSİN

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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