Early Mobilisation of the Distal Radius Fracture

NCT ID: NCT06258928

Last Updated: 2025-09-03

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

15 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-03-04

Study Completion Date

2024-09-30

Brief Summary

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The goal of this clinical trial is to demonstrate the effectiveness of early therapy in 14 patients with a distal radius fracture DRF resulting from injury, as the study group. Assess hand function of patients who underwent surgical repair of distal radius fractures using the open reduction internal fixation method (ORIF), compared to their nonoperated limb, after 6 months of early rehabilitation.

The main questions it aims to answer are:

1. Significantly faster recovery of independence from daily activities by the patient.
2. For economic reasons, patients often expect to return to work as soon as possible.

Participants will be subjected to functional examination to assess hand function of patients who underwent surgical repair of distal radius fractures using the open reduction internal fixation method.

Detailed Description

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Conditions

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Secondary Prevention

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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patients with a distal radius fracture

Functional examination included evaluating range of motion (ROM), grip strength, and isokinetic evaluation of force moments (Biodex) for wrist flexion, extension, forearm pronation, and forearm supination. Michigan's questionnaire and the Disability of the Arm, Shoulder, and Hand (DASH) questionnaire were used to subjectively evaluate the effects of therapy.

Functional examination

Intervention Type DIAGNOSTIC_TEST

Compared to nonoperated limb, after 6 months of early rehabilitation.

Interventions

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Functional examination

Compared to nonoperated limb, after 6 months of early rehabilitation.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* age range 18-60 years
* distal radius fracture
* ORIF procedure
* hand stabilisation plate (Medartis)

Exclusion Criteria

* delayed rehabilitation protocol
* algodystrophy
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Józef Piłsudski University of Physical Education

OTHER

Sponsor Role lead

Responsible Party

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Magdalena Kolasińska

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Terapia Ręki Magda Kolasińska

Warsaw, Masovian Voivodeship, Poland

Site Status

Countries

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Poland

Other Identifiers

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Radius Fracture

Identifier Type: -

Identifier Source: org_study_id

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