Sensorimotor Training for Wrist Fractures
Trial Summary
What is the purpose of this trial?
The purpose of this study is to compare the short-term outcomes of individuals who have surgery (volar plate) for a wrist (distal radius) fracture who have routine hand therapy treatment versus routine hand therapy treatment and sensorimotor activities. Individuals who meet inclusion criteria at the facilities collecting data will be invited to participate. If they agree to participate, they will randomly and blindly (via concealed envelopes) be assigned to the control (routine treatment) or the sensorimotor treatment group. Data collection will occur at 3- and 6-weeks post initiation of skilled therapy and will include measurement of joint position sense, function via the Patient Rated Wrist and Hand, pain via the Numeric Pain Rating Scale, and range of motion at the digits and wrist.
Do I need to stop my current medications for the trial?
The trial information does not specify whether you need to stop taking your current medications.
What data supports the effectiveness of the treatment Sensorimotor Training for wrist fractures?
Research shows that patients recovering from wrist surgery may experience faster sensorimotor improvements when using a comprehensive sensorimotor treatment protocol compared to standard care, although not all improvements were significant. This suggests that sensorimotor training could be beneficial in addressing sensorimotor deficits after wrist fractures.12345
Is sensorimotor training safe for treating wrist fractures?
How does sensorimotor training differ from other treatments for wrist fractures?
Sensorimotor training for wrist fractures is unique because it focuses on improving the sensorimotor and proprioception (awareness of body position) functions that are often impaired after wrist surgery. Unlike standard treatments, this approach aims to enhance the feedback loops between the brain and wrist, potentially leading to faster recovery of wrist function.3461011
Eligibility Criteria
This trial is for English-speaking adults over 18 who've had wrist surgery with a volar plate to fix a broken distal radius. They must be able to attend weekly occupational therapy sessions.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive either traditional hand therapy or traditional hand therapy with sensorimotor activities
Follow-up
Participants are monitored for safety and effectiveness after treatment
Treatment Details
Interventions
- Sensorimotor Training
Find a Clinic Near You
Who Is Running the Clinical Trial?
Hand Surgery Associates LLC
Lead Sponsor
Touro University Nevada
Collaborator
Orthopaedic Specialty Group PC, Fairfield
Collaborator