NCT06304428Enrolling by invitation
Prevention of Injury in Skilled Nursing Facilities Through Optimizing Medications
Source: ClinicalTrials.gov · Last updated 16 Jan 2026
Brief summary (registry, in English)
The goal of this clinical trial is to compare three care models for optimizing medications and preventing falls with broken bones in patients receiving rehabilitation after a hospitalization for a broken bone. The primary outcome is injurious falls, with secondary outcomes measuring how the process of care is changed and capturing patient-reported outcomes valued by stakeholders. The main questions this study aims to answer are: * Which of the three models is more effective in preventing falls with fractures? * What are the differences in patient-centered outcomes amongst the three models? These include pain, depression, anxiety, sleep, medication side effect burden, and fear of falling. * What are the differences in osteoporosis treatment and medication burden? The three care models are: a Deprescribing Care Model designed to reduce or stop fall-related medications, a Bone Heath Service Model designed to provide osteoporosis evaluation and management, and an Injury Prevention Service Model offering both services. 42 SNFs will participate in this study. The three models will be incorporated into the routine care of patients at these facilities who are receiving rehabilitation after a hospitalization for a fracture. All care models will be delivered remotely to patients in the SNF and after they transition home by a post-fracture nurse consultant supported by an interprofessional team. This study has three aims. See Detailed Description for more details. This ClinicalTrials.gov record represents the Comparative Effectiveness Aim of the protocol.
- Status (registry)
- Enrolling by invitation
- Study type
- Interventional
- Enrollment
- 3780 (estimated)
- First submitted
- 5 Mar 2024
- Start date
- 30 Sept 2024
- Primary completion date
- 1 Jul 2028
- Lead sponsor
- Duke University
- Diseases
- Osteoporosis
- NCT number
- NCT06304428
What you commit to
- Study type: Interventional
- Planned participants: 3780
- From 30 Sept 2024 to the primary completion date, 1 Jul 2028
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patient discharged or died prior to completion of a medication optimization plan
Other illness
- Non-osteoporotic fracture (e.g. facial, digital, skull, at site of tumor or infection)
Other
- Eligible for Hospice or palliative care
Who the study is looking for
- Aged 65 years or greater
- Admitted to an enrolled SNF after hospitalized fracture
- Completion of a medication optimization plan
Age in the registry: 65 years to - · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Marcus Institute for Aging Research, Hebrew SeniorLife Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Duke University School of Medicine Coordinator of this site? Confirm its status | Durham | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.