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Clinical Trials/NCT06724484
NCT06724484
Not yet recruiting
Not Applicable

Post-operative Anxiety and Depression Among Older Adults Who Undergo Surgery for Fragility Fractures

University of Southampton1 site in 1 country60 target enrollmentJanuary 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fractures in the Elderly
Sponsor
University of Southampton
Enrollment
60
Locations
1
Primary Endpoint
Hospital Anxiety and Depression Scale
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

Patients who present with falls and fractures can experience increased symptoms of depression and anxiety due to the trauma of falling, hospitalisation and surgery. Additionally after surgery, patients may be limited in their mobility, resulting in a loss in their independence which can lead to further feelings of frustration and helplessness. In this study we want to know how common this problem is among older people who are admitted to hospital with broken bones and subsequently receiving surgery.

We will use a questionnaire called the Hospital Anxiety and Depression Scale (HADS) to explore this. We will recruit 60 patients for this study, 30 participants who received operative management and a further 30 participants who did not receive surgery for comparison. Patients who are not able to consent to the study or those who are not able to complete the questionnaire will not be recruited. We will collect routine data from the patients to provide a description of the patients that we are studying. Patients will complete the HADS questionnaire once during their hospital stay and then in 1 month's time. We will contact patients through telephone for the 1 month follow up.

This study will enable us to determine how common are the symptoms of anxiety and depression among this group of patients. This will help raise awareness of the problem which may prompt further intervention and management plan to address this important issue.

Registry
clinicaltrials.gov
Start Date
January 2025
End Date
December 2025
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 65 years and above
  • Received operative or non-operative management of fragility fracture
  • Able to provide written consent

Exclusion Criteria

  • Patients receiving end of life care
  • Patients with known diagnosis of severe dementia and/ or lack capacity to consent
  • Non-fragility fracture

Outcomes

Primary Outcomes

Hospital Anxiety and Depression Scale

Time Frame: This will be measured at baseline and at 1 month follow up.

Study Sites (1)

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