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The Nottingham spinal health study

Nottingham Spinal Health (NoSH) Study: A cohort study of vertebral fragility fractures admitted to hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN14436287
Enrollment
100
Registered
2016-12-20
Start date
2016-09-28
Completion date
Unknown
Last updated
2020-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vertebral fractures, including those in patients with osteoporosis Musculoskeletal Diseases 1. Osteoporosis 2. Vertebral fractures

Interventions

Patients with a diagnosed or suspected diagnosis of an acute vertebral fragility fracture will be invited to participate in the study. Data collection will be conducted on admission, at discharge from

Sponsors

Nottingham University Hospitals NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adults aged 50 years and over 2. Admitted to hospital with either a low trauma or atraumatic vertebral fragility fracture or suspected vertebral fragility fracture pending radiology investigation. A low trauma fracture is a fracture sustained after a fall from a standing height or less. A diagnosis of vertebral fracture is made radiologically (i.e. x-ray imaging, computerised tomography (CT), magnetic resonance imaging (MRI) of the spine) or bone (scintigraphy) scan. 3. While in hospital was diagnosed with a vertebral fragility fracture unrelated to their index admission

Exclusion criteria

Exclusion criteria: 1. Patients without a vertebral fracture 2. Patients admitted electively to hospital for management of their vertebral fracture 3. Patients transferred from another hospital 4. Vertebral fracture sustained as a result of a high impact injury, e.g. road traffic accident, fall down a flight of stairs, etc. 5. Patients presenting with a concomitant fracture elsewhere 6. Patients admitted to hospital under a major trauma pathway 7. Patients with known or suspected malignancy 8. Patients with known primary bone disorder (e.g Paget’s disease) other than osteoporosis 9. Patients terminally ill or moribund

Design outcomes

Primary

MeasureTime frame
1. Pain is measured using an 11 point numeric rating scale at baseline (on admission to hospital), on discharge from hospital and at 6 months 2. Mood is measured using the Geriatric Depression Scale at baseline (on admission to hospital) and at 6 months 3. Cognition is measured using the Montreal Cognitive Assessment at baseline (on admission to hospital) and at 6 months 4. Disability is measured using the Elderly Mobility Scale, Barthel Index, Nottingham Extended Activities of Daily Living and Roland Morris Disability Questionnaire at baseline (on admission to hospital) and at 6 months

Secondary

MeasureTime frame
1. Hospital inpatient mortality and overall mortality are measured by analysing healthcare records at 6 months 2. Hospital related outcomes measured by analysing hospital paper and electronic healthcare records on patients discharge - length of stay, discharge destination/changes in residency, hospital related complication (hospital acquired infection, pressure sore, venous thromboembolic event, delirium and neurological impairment) 3. Quality of life post-hospitalisation for vertebral fractures is measured using the EQ-5D measured at 6 months 4. Healthcare resource utilisation after hospital discharge is measured through self or proxy reporting at 6 months

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026