Bone Strength and Physical Activity in Patients With a Recent Clinical Fracture

NCT05138640 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2021-12-01

No results posted yet for this study

Summary

The risk for a subsequent fracture is significantly higher in patients presenting with a fracture compared to individuals without a previous fracture and is highest within the first 2 years after the initial fracture. The risk for a subsequent fracture is not dependent of BMD as measured by conventional DXA. In recent studies, it has been shown that HRpQCT measurements provide information about bone structure, bone quality and bone strength in addition to BMD measurements. Diagnostic strategies should be focussed on bone quality and bone strength and fall prediction in the patients at high risk for falls, subsequent fracture and mortality such as patients with a recent fracture. Therefore, the investigators conduct a prospective observational study in 500 patients aged 50 years and older who present with a clinical fracture for evaluation of bone strength, physical activity, falls, subsequent fractures and mortality during a follow-up period of 3 years.

Conditions

  • Fractures, Bone
  • Patient Fall
  • Osteoporosis
  • Physical Activity

Interventions

OTHER

Not applicable. The study is designed as an observational cohort study

Not applicable. The study is desigend as an observational cohort study

Sponsors & Collaborators

  • Joop P.W. van den Bergh

    lead OTHER

Principal Investigators

  • J PW van den Bergh, MD, PhD · VieCuri Medical Centre

Eligibility

Min Age
50 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-10-31
Primary Completion
2019-07-31
Completion
2019-07-31

Countries

  • Netherlands

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05138640 on ClinicalTrials.gov