Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Patients 75 years or older with a hip fracture
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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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