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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date December 2019
Source Oregon Health and Science University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


Recruitment information / eligibility

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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Digital Media Based Physical Therapy
This intervention is a modified post immobilization protocol. This will include giving the patients a USB drive loaded with a 12 week 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.
Traditional Physical Therapy
This intervention is a 12 week therapist supervised clinic-based therapy protocol.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Oregon Health and Science University

Outcome

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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