Digital Media Based Physical Therapy Post Distal Radius Fracture
- Conditions
- Distal Radius Fracture
- Interventions
- Other: Traditional Physical TherapyOther: 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
- Patients undergoing operative treatment for distal radius fractures.
- 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
Group Intervention Description Traditional Therapy Traditional Physical Therapy The traditional group will have clinic-based physical therapy protocol. Digital Media Therapy Digital Media Based Physical Therapy The 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
Name Time Method 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
Name Time Method Visual Analog Pain Scale 6 weeks, 12 weeks, and 6 months Patient-Reported Outcome, Scale: 0 (no pain) - 10 (most severe pain)
Wrist Circumference 6 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 Strength 6 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 Motion 6 weeks, 12 weeks, and 6 months Wrist flexion, extension, pronation, supination, ulnar deviation, radial deviation