Cross-sectoral Rehabilitation of Older High-risk Patients With Hip Fracture (NCT06304584) | Clinical Trial Compass
CompletedNot Applicable
Cross-sectoral Rehabilitation of Older High-risk Patients With Hip Fracture
Denmark53 participantsStarted 2023-05-15
Plain-language summary
The goal of this observational study is to learn about and monitor the cross-sectoral rehabilitation process in older high-risk patients treated for at fragility fracture of the hip.
The main questions aim to answer:
* how patients are doing up to one year after hip fracture surgery on different outcomes across the continuum of rehabilitation being offered
* what expectations, experiences and satisfaction patients have for the overall rehabilitation process after a hip fracture
Participants age 65 and above with home address in Frederiksberg municipality, living in own home, admitted and treated for at hip fracture at Department of Orthopedic Surgery, Bispebjerg Hospital, will be asked for participation.
Who can participate
Age range
65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
Undergone surgery for hip fracture and admitted to department M1, Bispebjerg-Frederiksberg Hospital
Living in Frederiksberg municipality and being admitted from own home, or a 24 hour temporary setting in the municipality
Exclusion Criteria:
Living permanent in nursing home or is on the way to a permanent nursing home from a 24-hour setting.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Recovery of pre-fracture function
Timeframe: Recovery of pre-fracture function at 3-4 months post-fracture as primary outcome
Trial details
NCT IDNCT06304584
SponsorUniversity Hospital Bispebjerg and Frederiksberg