Novel Exercises to Facilitate Recovery of Supination and Pronation for Distal Radius Fractures Managed With a Volar Plate

NCT05850325 — Not applicable, Unknown, 42 participants, Indiana Hand to Shoulder Center

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RegistryNCT05850325
StatusUnknown
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: none, other
Enrollment42 (Estimated)
SponsorIndiana Hand to Shoulder Center (Other)
ConditionsDistal Radius Fracture
InterventionsGroup 1 Elbow Flexed at 90 Degrees, Group 2 Elbow Fully Flexed (Other)
Datesstart 2022-12-16, primary completion 2023-12-01 (estimated), completion 2024-04-01 (estimated), first posted 2023-05-09, last updated 2023-05-09
Locations1 site in United States

Related Papers Related Patents Related Grants Related Experts
All trials for Distal Radius Fracture All trials of Group 1 Elbow Flexed at 90 Degrees All trials of Group 2 Elbow Fully Flexed

-Summary

The primary objective of this study is to evaluate the influence of elbow position on achieving forearm supination and pronation and wrist ROM postoperatively. It is anticipated the results will show recovery of functional motion in a shorter period of time (27 days average). As for the secondary objective of the study, it is anticipated there will be limited pain and cost-containment. These data elements will serve as secondary factors to evaluate.

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+Detailed description

The current standard of care for forearm range of motion exercises is to position the elbow in 90 degrees of flexion at the side of the body for both supination and pronation.5,6 This study will compare standard of care forearm rotation exercises to exercising with the elbow in extension to facilitate pronation and exercising with the elbow in full flexion to facilitate supination in patients who have undergone surgery with a volar plate for distal radius fractures. We hypothesize that forearm motion will be achieved in a shorter number of days and with a greater arc of motion when the exercises are done in extremes of elbow flexion and extension.

This will be a prospective, unblinded, randomized study to evaluate forearm range of motion across two groups:

Control Group: subjects will be instructed to exercise the forearm with the elbow positioned by their side, in 90° of flexion.

Test Group: subjects will be instructed to exercise the forearm with their elbow fully flexed to achieve supination and the elbow extended to achieve pronation.

Randomization will occur post-operatively after the patient has signed consent to participate. Randomization will occur through a computerized random allocation and groups will be assigned by the Clinical Research Manager or designee.

+Arms and interventions

ArmTypeInterventionsDescription
Group 1: Elbow Flexed at 90 DegreesOtherOther: Group 1 Elbow Flexed at 90 Degreessubjects will be instructed to exercise the forearm with the elbow positioned by their side, in 90° of flexion.
Group 2: Elbow Fully FlexedExperimentalOther: Group 2 Elbow Fully Flexedsubjects will be instructed to exercise the forearm with their elbow fully flexed to achieve supination and the elbow extended to achieve pronation.
  • Group 1 Elbow Flexed at 90 Degrees (Other), also known as Elbow Flexed to 90 Degrees: subjects will be instructed to exercise the forearm with the elbow positioned by their side, in 90° of flexion.
  • Group 2 Elbow Fully Flexed (Other), also known as Elbow Fully Flexed: subjects will be instructed to exercise the forearm with their elbow fully flexed to achieve supination and the elbow extended to achieve pronation.

+Outcome measures

Primary outcomes

  • Range of Motion [6 Months]: forearm supination and pronation and wrist ROm

Secondary outcomes

  • Upper Limb Functional Index (ULFI) [6 Months]: PROM functional questionnaire
  • QuickDisability of the Arm Shoulder Hand (DASH) [6 Months]: PROM - functional questionnaire

+Eligibility

Sex: All, ages: 18 Years to any

Inclusion Criteria:

* • Subjects 18 years of age and older

  * Subjects with distal radius fractures with a volar plate
  * Subjects attending therapy at the Indiana Hand to Shoulder Center or affiliated satellites.
  * Subjects that attend the initial therapy visit between 5 and 10 days postoperative and begin the home therapy program (patient handout)

Exclusion Criteria:

* • Subjects under the age of 18

  * Additional surgical procedures or other factors preventing early active ROM of the forearm and/or wrist within the initial 10 days following surgery
  * Pre-existing medical conditions or injuries with resultant limitation in elbow, forearm or wrist ROM, patient-reported limited function, or limited ability to comply with home program (cognitive skills).
  * While undergoing therapy the initial 6 weeks, subjects provided with custom-fabricated or pre-fabricated devices, orthoses, or braces for the specific purpose of passively improving ROM of the elbow, forearm or wrist during the initial 6 weeks of therapy.

+Locations (1)

FacilityCityCountryStatus
Indiana Hand to Shoulder CenterIndianapolis, IndianaUnited States