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Digital Media Based Physical Therapy Post Distal Radius Fracture

Not Applicable
Completed
Conditions
Distal Radius Fracture
Interventions
Other: Traditional Physical Therapy
Other: Digital Media Based Physical Therapy
Registration Number
NCT04194749
Lead Sponsor
Oregon Health and Science University
Brief Summary

This trial aims to develop and test the efficacy of a digital media based physical therapy protocol on patients after surgical fixation and non-operative treatment of distal radius fractures.It is hypothesized that there will not be a difference in outcomes for patients after surgical fixation of distal radius fractures with traditional physical therapy and digital media based therapy

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
51
Inclusion Criteria
  • Patients undergoing operative treatment for distal radius fractures.
Exclusion Criteria
  • Poly-trauma patients with significant previous diagnosis of dementia, previous traumatic brain injury, or other reason for significant altered mental status that would interfere with their participation in therapist directed or digital based therapy will be excluded.
  • Patients who present to Oregon Health & Science University for physical therapy who will be treated by a physician at another non Oregon Health & Science University facility will be excluded.
  • Patients who are not proficient in the English language will be excluded.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Traditional TherapyTraditional Physical TherapyThe traditional group will have clinic-based physical therapy protocol.
Digital Media TherapyDigital Media Based Physical TherapyThe digital media based group will receive a modified post immobilization protocol. This will include giving the patients a Universal Serial Bus (USB) drive loaded with a 12 week physical therapy protocol presented in digital form with videos and graphical representations of exercises to be done. They will also have access to the videos and multimedia on the Oregon Health \& Science University website.
Primary Outcome Measures
NameTimeMethod
Abbreviated version of the Disabilities of the Arm, Shoulder and Hand (QuickDASH)12 weeks

Patient-Reported Outcome, Scale: 0 (no disability) - 100 (most severe disability)

Secondary Outcome Measures
NameTimeMethod
Visual Analog Pain Scale6 weeks, 12 weeks, and 6 months

Patient-Reported Outcome, Scale: 0 (no pain) - 10 (most severe pain)

Wrist Circumference6 weeks, 12 weeks, and 6 months

Anthropometric measurement

Abbreviated version of the Disabilities of the Arm, Shoulder and Hand (QuickDASH)6 weeks, 6 months

Patient-Reported Outcome, Scale: 0 (no disability) - 100 (most severe disability)

Hand Grip Strength6 weeks, 12 weeks, and 6 months

Strength measurement

Veterans RAND 12-item Health Survey (VR-12)6 weeks, 12 weeks, and 6 months

Patient-Reported Outcome

Wrist Range of Motion6 weeks, 12 weeks, and 6 months

Wrist flexion, extension, pronation, supination, ulnar deviation, radial deviation

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