Distal Radius Fracture Clinical Trial
Official title:
Physical Therapy After Distal Radius Fracture; Traditional Versus Digital Media Based Therapy Protocol
NCT number | NCT04194749 |
Other study ID # | 11330 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 1, 2015 |
Est. completion date | April 30, 2019 |
Verified date | December 2019 |
Source | Oregon Health and Science University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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
Status | Completed |
Enrollment | 51 |
Est. completion date | April 30, 2019 |
Est. primary completion date | June 30, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
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. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Oregon Health and Science University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Abbreviated version of the Disabilities of the Arm, Shoulder and Hand (QuickDASH) | Patient-Reported Outcome, Scale: 0 (no disability) - 100 (most severe disability) | 12 weeks | |
Secondary | Abbreviated version of the Disabilities of the Arm, Shoulder and Hand (QuickDASH) | Patient-Reported Outcome, Scale: 0 (no disability) - 100 (most severe disability) | 6 weeks, 6 months | |
Secondary | Visual Analog Pain Scale | Patient-Reported Outcome, Scale: 0 (no pain) - 10 (most severe pain) | 6 weeks, 12 weeks, and 6 months | |
Secondary | Veterans RAND 12-item Health Survey (VR-12) | Patient-Reported Outcome | 6 weeks, 12 weeks, and 6 months | |
Secondary | Wrist Range of Motion | Wrist flexion, extension, pronation, supination, ulnar deviation, radial deviation | 6 weeks, 12 weeks, and 6 months | |
Secondary | Hand Grip Strength | Strength measurement | 6 weeks, 12 weeks, and 6 months | |
Secondary | Wrist Circumference | Anthropometric measurement | 6 weeks, 12 weeks, and 6 months |
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