Actively Recruiting

Phase Not Applicable
Age: 75Years +
All Genders
ID05904353

Collaboration to Improve Bone Health After Hip Fracture Using Nurse-Assisted Zoledronic Acid Treatment

Led by University Hospital, Akershus · Updated on 2024-02-05

200

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a new approach to improve care coordination between hospitals and primary care for patients aged 75 or older who have suffered a hip fracture. The study focuses on osteoporosis treatment using zoledronic acid infusions combined with vitamin D and calcium supplements to prevent further fractures. The trial aims to test if ambulant nurses assisting general practitioners (GPs) can increase the number of patients receiving recommended annual zoledronic acid infusions over three years after their fracture. Participants receive an initial infusion of zoledronic acid 5 mg at the hospital after their femoral neck fracture and are then followed in one of two ways based on their region. In intervention regions, ambulant nurses support GPs with administering zoledronic acid yearly for three years. In control regions, patients receive usual care where GPs are responsible for follow-up and annual infusions guided by discharge summaries. The study is designed as a cluster randomized controlled trial with regions assigned to intervention or control groups. During the study, patients from both groups are asked to complete a questionnaire after one year, reporting if they received zoledronic acid as recommended. The main outcome is whether patients are offered treatment at the one-year follow-up. The trial includes safety monitoring and data collection over three years, with an estimated total of 200 patients to account for mortality. It seeks to establish practical procedures for nurse-assisted osteoporosis treatment in primary care settings to improve patient care continuity after hospital discharge.

CONDITIONS

Brief Title

A Study to Improve the Collaboration Between Primary and Secondary Health Care on the Treatment of Osteoporosis After a Hip Fracture.

Who Can Participate

Age: 75Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 75 years or older with a hip fracture
Not Eligible

You will not qualify if you...

  • Refuse treatment
  • Another treatment of osteoporosis is indicated
  • Guest patient, do not live in the admission area
  • Dementia

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - 1 year

Participants receive zoledronic acid treatment either through ambulant nurse-assisted administration or usual care with general practitioner follow-up and annual infusions.

Annual visits for zoledronic acid infusion

Trial Site Locations

Total: 1 location

1

Orthopedic Department, Akershus University Hospital

Lørenskog, Akershus, Norway, 1478

Actively Recruiting

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Research Team

J

Jakob Vangen Nordbø, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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