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Is Sensorimotor Training Effective Following a Distal Radius Fracture?

NCT06299228 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2024-04-29

No results posted yet for this study

Summary

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.

Conditions

  • Distal Radius Fractures

Interventions

OTHER

Experimental Group

Sensorimotor intervention, active range of motion, active assisted range of motion, strengthening

OTHER

Control Group

Active range of motion, active assisted range of motion and strengthening

Sponsors & Collaborators

  • Touro University Nevada

    collaborator OTHER

  • Orthopaedic Specialty Group PC, Fairfield

    collaborator OTHER

  • Hand Surgery Associates LLC

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-30
Primary Completion
2025-04-30
Completion
2025-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06299228 on ClinicalTrials.gov