Rehabilitation Following Displaced Proximal Humerus Fractures
NCT ID: NCT05302089
Last Updated: 2025-02-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
60 participants
INTERVENTIONAL
2022-05-05
2025-01-20
Brief Summary
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Detailed Description
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It is assumed that rehabilitation delivered as structured training benefits patients with PHFs, but this is not known from current evidence. It is possible that patients are even harmed with intensive training programmes. Most RCTs with a non-surgically treated group use the same exercise intervention in the two groups to best identify the difference between surgery and non-surgical treatment. Therefore, the effect of training cannot be concluded from these studies. This is supported by an expectation of more nonsurgically treated displaced PHFs due to the growing evidence of no benefit from surgery. The current study is a prerequisite for future rehabilitation studies comparing different training modalities. Therefore, this study aims is to evaluate the effectiveness of usual rehabilitation care after displaced PHF compared with one-time physiotherapy instruction.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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One-time physiotherapy instruction
One-time physiotherapy instruction and no usual rehabilitation care
Pain management and shoulder bandage
All Patients receive standard pain management according to the local guidelines and a sling and swathe on the day of injury. After 10 to 14 days, all patients will receive a sling for optional use for one to two weeks and be randomized after oral and written informed consent.
One-time physiotherapy instruction
Patients are offered a one-time physiotherapy instruction about the course of pain and suggestions for quick and safe return to activities of daily living within the first three months post-injury.
Usual rehabilitation care
One-time physiotherapy instruction and usual rehabilitation care
Pain management and shoulder bandage
All Patients receive standard pain management according to the local guidelines and a sling and swathe on the day of injury. After 10 to 14 days, all patients will receive a sling for optional use for one to two weeks and be randomized after oral and written informed consent.
One-time physiotherapy instruction
Patients are offered a one-time physiotherapy instruction about the course of pain and suggestions for quick and safe return to activities of daily living within the first three months post-injury.
Usual rehabilitation care
At the visit 10-14 days after the injury, the orthopaedic consultant (senior author SB) will refer the patient to usual rehabilitation care with a physiotherapist in a municipality close to the patient´s home. The physiotherapist then schedules the start date, typically three weeks after the injury. The rehabilitation content and duration is planned according to the choice of the local treating physiotherapist in consultation with the patient.
Interventions
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Pain management and shoulder bandage
All Patients receive standard pain management according to the local guidelines and a sling and swathe on the day of injury. After 10 to 14 days, all patients will receive a sling for optional use for one to two weeks and be randomized after oral and written informed consent.
One-time physiotherapy instruction
Patients are offered a one-time physiotherapy instruction about the course of pain and suggestions for quick and safe return to activities of daily living within the first three months post-injury.
Usual rehabilitation care
At the visit 10-14 days after the injury, the orthopaedic consultant (senior author SB) will refer the patient to usual rehabilitation care with a physiotherapist in a municipality close to the patient´s home. The physiotherapist then schedules the start date, typically three weeks after the injury. The rehabilitation content and duration is planned according to the choice of the local treating physiotherapist in consultation with the patient.
Eligibility Criteria
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Inclusion Criteria
Prior to first visit in the outpatient clinic all patients with PHFs will be screened for eligibility based on initial radiographs and medical records by an experienced orthopaedic consultant (senior author SB) at Zealand University Hospital, Køge, Denmark. The senior author classifies fracture categories.
• Patients should be cognitively capable of answering patient-reported outcome measures.
Exclusion Criteria
* Diagnosed with dementia or institutionalized
* Does not understand written and spoken guidance in Danish
* Pathological fracture or previous fracture in the same proximal humerus
* Concomitant injury or fracture.
* Polytrauma, high-energy trauma, or multiple fractures
* Fracture dislocation or articular surface fracture
* Isolated tuberosity fracture
* Fractures not expected to heal by non-surgical treatment (no bony contact between head and shaft in both views)
* The senior author considers the patient unsuitable to attend the study for medical reasons (substance abuse, affective or psychotic disorders, apoplexy, chronic pain, malignant disease)
* Symptomatic glenohumeral osteoarthritis, rheumatoid arthritis, or rotator cuff-arthropathy
60 Years
ALL
No
Sponsors
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University of Southern Denmark
OTHER
University of Copenhagen
OTHER
Zealand University Hospital
OTHER
Responsible Party
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Principal Investigators
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Behnam Liaghat, MSc
Role: PRINCIPAL_INVESTIGATOR
Zealand University Hospital, University of Southern Denmark
Stig Brorson, PhD
Role: STUDY_DIRECTOR
Zealand University Hospital, University of Copenhagen
Locations
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Department of Orthopaedics, Zealand University Hospital
Køge, , Denmark
Countries
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References
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Liaghat B, Brorson S. Effect of structured rehabilitation versus non-structured rehabilitation following non-surgical management of displaced proximal humerus fractures: a protocol for a randomised clinical trial. BMJ Open. 2022 Oct 17;12(10):e064156. doi: 10.1136/bmjopen-2022-064156.
Other Identifiers
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PHF_rehab
Identifier Type: -
Identifier Source: org_study_id
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