Is Sensorimotor Training Effective Following a Distal Radius Fracture?

Hand Surgery Associates LLC

Status: Enrolling

Conditions: Distal Radius Fractures

Treatments: Other: Control Group; Other: Experimental Group

Study type: Interventional

Funder types: Other

Identifiers

NCT06299228

HSA

Details and patient eligibility

About

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.

Full 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.

Enrollment: 50 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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50 participants in 2 patient groups

Experimental Group

Experimental group

Description:

The experimental group will receive sensorimotor intervention and traditional hand therapy

Treatment:

Other: Experimental Group

Control Group

Experimental group

Description:

Control Group will receive Hand Therapy only

Treatment:

Other: Control Group