Recruiting

Sensorimotor Training

Sponsor:

Hand Surgery Associates LLC

Code:

NCT06299228

Conditions

Distal Radius Fractures

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Experimental Group

Control Group

Study Details

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.

Conditions

Distal Radius Fractures

Study ID

NCT06299228

Start date

Apr, 2024

Status verified date

Apr, 2024

Completion date

Apr, 2025

Anticipated

Primary completion date

Apr, 2025

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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

Study Design

Enrollment

50 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Experimental Group

The experimental group will receive sensorimotor intervention and traditional hand therapy

experimental: Control Group

Control Group will receive Hand Therapy only

Interventions

Experimental Group

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

Control Group

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

Primary outcome measure

  • Active Joint Position Sense (AJPS) [ Time Frame: Baseline, 3 and 6 weeks ]

Central Contacts and Locations

Central contacts

Locations

Hand Surgery Associates

Recruiting

Olyphant, Pennsylvania, United States, 18447

Contacts

More Information

Sponsor

Hand Surgery Associates LLC

Last update posted

Apr 29, 2024

Last verified

Apr, 2024

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Hand Surgery Associates LLC on 2024-04-29.