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OpenTrials
Completed

NCT Number: NCT06724484

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

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 the investigators want to know how common this problem is among older people who are admitted to hospital with broken bones and subsequently receiving surgery.

The investigators 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. The investigators will collect routine data from the patients to provide a description of the patients. Patients will complete the HADS questionnaire once during their hospital stay and then in 1 month's time. The investigators will contact patients through telephone for the 1 month follow up.

This study will enable the investigators 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.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Academic Geriatric Medicine, University of Southampton

Southampton, Hampshire, SO16 6YD, United Kingdom

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Surgical management of fracture

Procedure

Surgical management of fracture

No intervention

Other

No intervention

Primary outcomes

  1. Hospital Anxiety and Depression Scale

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

    The Hospital Anxiety and Depression scale (HADS) consists of 14 items split into two 7-item subscales for anxiety (HADS-A) and depression (HADS-D), each scored 0-3, with subscale totals ranging from 0 to 21; scores of 0-7 are normal, 8-10 borderline, and 11-21 indicating an abnormal score that will trigger further clinical assessment for anxiety and/or depression.

Sponsors and collaborators

Lead sponsor

University of Southampton

Other

Registry information

Acronym: FFAD

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Dec 9, 2024
Registry last updated
May 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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