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Is Sensorimotor Training Effective Following a Distal Radius Fracture?

Sensorimotor Training and Hand Therapy Versus Traditional Hand Therapy Alone Following a Distal Radius Fracture With Volar Plate Fixation: A Randomized Controlled Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06299228
Enrollment
50
Registered
2024-03-07
Start date
2024-04-30
Completion date
2025-04-30
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Distal Radius Fractures

Brief 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.

Detailed description

The study is an interventional study investigating the effectiveness of sensorimotor activities in addition to traditional occupational therapy intervention versus traditional intervention only for patients following a distal radius fracture with volar plate fixation. A convenience sample of patients from 2 outpatient orthopedic hand therapy departments will be invited to participate in the study. The treatment for both groups will be identical with one group receiving the addition of sensorimotor activities. Participants will be divided into one of the two groups. They will be made aware that at any point they can choose to no longer participate in the study, and it will not affect their treatment.

Interventions

OTHERExperimental Group

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

OTHERControl Group

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

Sponsors

Touro University Nevada
CollaboratorOTHER
Orthopaedic Specialty Group PC, Fairfield
CollaboratorOTHER
Hand Surgery Associates LLC
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Distal radius fracture with volar plate fixation * Understand English * 18 years or older * Available to attend skilled occupational therapy visits a minimum of 1x per week.

Exclusion criteria

* Prior surgery to the involved wrist/hand * Cognitive impairment * Distal radius fracture managed by casting or by another means of fixation

Design outcomes

Primary

MeasureTime frameDescription
Active Joint Position Sense (AJPS)Baseline, 3 and 6 weeksRange of motion measurement for the wrist, the measurements are recorded in degress of motion and the greater the number of degrees is reflective of greater sensorimotor deficit

Secondary

MeasureTime frameDescription
Patient Rated Wrist and Hand EvaluationBaseline, 3 and 6 weeksPatient reported outcome measurement with a 0-100 range, 0 indicating no functional deficit and 100 indicating the worst functional scale

Countries

United States

Contacts

Primary ContactNancy Naughton, OTD
nancynaughton10@gmail.com5707808681
Backup ContactKristen Valdes, OTD
kvaldes2@turo.edu9414685500

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026