RecruitingNCT07633483

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

Assessment of the Relationship Between Preoperative Anxiety Level Measured by the Hamilton Anxiety Rating Scale and Frailty Score Assessed by the FRAIL Scale in Elderly Patients Aged 65 Years and Older Scheduled for Elective Hip Arthroplasty: A Prospective Observational Single-Center Study


Sponsor

Başakşehir Çam & Sakura City Hospital

Enrollment

142 participants

Start Date

Dec 1, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

Frailty is a state of vulnerability resulting from decreased physiological reserve across multiple organ systems, impairing an individual's ability to withstand stressors. As the elderly population grows worldwide, the proportion of older adults undergoing surgical procedures continues to rise, and frailty is expected to become increasingly prevalent among surgical candidates. Anxiety is one of the most common psychiatric conditions, affecting approximately one in three individuals globally. Preoperative anxiety may negatively influence surgical outcomes, particularly in older and more vulnerable patients. This prospective observational study aims to evaluate the relationship between preoperative anxiety level and frailty score in elderly patients aged 65 years and older scheduled for elective hip arthroplasty. Frailty will be assessed using the FRAIL Scale (Fatigue, Resistance, Ambulation, Illness, Loss of Weight), and anxiety will be measured using the Hamilton Anxiety Rating Scale (HAM-A). Secondary outcomes include the prevalence of frailty and anxiety, the effect of frailty on length of hospital stay, postoperative intensive care unit admission rates, and the relationship between frailty and preoperative laboratory and hemodynamic parameters.


Eligibility

Min Age: 65 Years

Inclusion Criteria4

  • 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

Exclusion Criteria5

  • 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

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(1)

Basaksehir Çam Ve Sakura City Hospital, İstanbul, Türkiye

Istanbul, Istanbul, Turkey (Türkiye)

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07633483


Related Trials