- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07556263
Mobility and Activity of Daily Living Outcomes After a Hip Fracture. (MOVE-HIP)
June 2, 2026 updated by: JointResearch
Mobility and Activity of Daily Living Outcomes After a Hip Fracture: Variabeles for Expectation.
Hip fractures in especially older adults cause severe clinical and functional impacts.
Despite improved surgical care, one year mortality remains 14-30%, and fewer than half of the survivors regain their pre-fracture functional status.
After a hip fracture, patients are primarily concerned with what they will be able to do in daily life.
Wihout accurate predictions of mobility and Activities of Daily Life (ADL) independence, it is difficult to set realistic expectations and make appropriate decisions regarding treatment and rehabilitation.
While there have been advancements in developing predictive models for mortality following hip fractures, there is a notable gap in models focused on predicting functional recovery.
This study aims to develop and validate a machine learning-based model that can predict mobility and ADL independence three months after obtaining a hip fracture.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
1200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Amsterdam, Netherlands
- Recruiting
- OLVG hospital
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Contact:
- Joint Research
- Phone Number: +31 20 5992757
- Email: jointresearch@olvg.nl
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
The study population will involve patients who have obtained a hip fracture between 01-01-2016 and 31-12-2025 and who were 18 years or older at the time of the injury.
To be included in the initial dataset it is necessary for the patient to have a value for baseline (pre-fracture) ADL independence and/or mobility, and to have an outcome at three months for ADL independence and/or mobility.
Description
Inclusion Criteria:
- Patient has been treated for a hip fracture in OLVG hospital betweek 01-01-2016 and 31-12-2025
- Patient was 18 years or older at the time of the injury
Exclusion Criteria:
- The patient does not grant permission for the use of their data for studies
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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"Estimated mobility 3 months, after obtaining a hip fracture" "Estimated ADL independence 3 months after obtaining a hip fracture"
Time Frame: ADL independence and mobility 3 months after a hip fracture
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For the outcome mobility participants get to know if they will be mobility independent (score 1-3 will get a 0) or mobility depenedent (score 4-5 will get a 0).
for the outcome ADL independence patients get a score indicating whether ADL is maintained/better (1) and else if ADL is deteriorated (0).
|
ADL independence and mobility 3 months after a hip fracture
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2016
Primary Completion (Actual)
December 31, 2025
Study Completion (Estimated)
December 31, 2027
Study Registration Dates
First Submitted
April 22, 2026
First Submitted That Met QC Criteria
April 22, 2026
First Posted (Actual)
April 29, 2026
Study Record Updates
Last Update Posted (Actual)
June 4, 2026
Last Update Submitted That Met QC Criteria
June 2, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- WO 26.020
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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