Range of Motion and Patients With Distal Radius Fractures

The Effect of Early vs. Delayed Range of Motion in the Outcome of Patients With Distal Radius Fractures

Hypothesis : Early active range of motion protocol after open reduction and internal fixation of a distal radius fracture with a volar fixed angle locking plate results in earlier return of functional motion, earlier return to work and improved functional outcomes compared delayed mobilization.

Specific Aim:

To compare early range of motion versus delayed motion protocol in distal radius fractures treated with open reduction and internal fixation with a volar fixed angle locking plate with respect to time to fracture union, range of motion, functional outcome measures, return to work and complications.

Study Overview

• Status: Completed
• Conditions: Radius Fractures
• Intervention / Treatment: Procedure: Physical therapy; Procedure: Physical Therapy

Detailed Description

You are scheduled for surgery of your broken wrist. Treatment of broken bones of the wrist, such as distal radius fractures, may require different types of treatment. For this study this type of fracture will be treated by surgery to place a plate with screws to the broken bone and then a plaster splint will be applied. After surgery, physical therapy will be started. Following surgery you will be assigned to one of four groups by the type of wrist fracture (broken bone) you have. Each person will by chance (the flip of a coin) be put in either the Early or Delayed Range of Motion groups. Those in the Early Range of Motion groups will begin exercises for motion starting 7 days after surgery. Those in the Delayed Range of Motion, will begin exercises for motion starting about five weeks after surgery. Once you begin the exercises to help you get back normal use of your wrist, you will have measurements of how much motion and strength you have in the wrist and hand that was fractured. The measurements will take about five minutes to complete. All participants will have an x-ray of the wrist at 2, & 6 weeks following surgery and if needed at other appointments. At each appointment you will be asked to fill out four questionnaires, asking about pain and how you are getting along with the broken bone in your wrist. The questionnaires will take about 20 minutes of your time to complete. At Week 26 you will be asked to record the amount of motion you have in both of your wrists on paper drawings as well as the measurements that we will make. Working with the drawings will take approximately five minutes. At Week 52 you will be asked two questions about how satisfied you are with the results of your surgery. Surgery, x-ray of your wrist, and exercise to help you get back motion of your broken wrist are all standard orthopedic practice for treating a broken wrist bone.

• Study Type: Interventional
• Enrollment (Actual): 39
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Minnesota
    • Rochester, Minnesota, United States, 55905
      • Mayo Clinic

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 85 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

The following criteria must be met to be enrolled:

1. Have a closed unstable distal radius fracture
2. Have a fracture classified as an AO Type A or C fracture, with or without an ulnar styloid fracture
3. Be a male or non-pregnant female at least 18 years of age.
4. Understand the requirements of the study and able to provide a written informed consent and comply with the study protocol
5. Have the ability to understand and provide written authorization for use and disclosure of personal health information

Exclusion Criteria:

Participants are excluded if they:

1. Have any of the following conditions

   1. Concomitant contralateral or ipsilateral upper extremity fractures
   2. Ipsilateral ulna (excluding styloid) fracture
   3. Open, multi-fragmentary fracture
   4. Artery or Nerve injury secondary to fracture
2. Have had a previous ipsilateral distal radius fracture in the 2 years prior to enrollment
3. Are currently on chemotherapy or radiation therapy
4. A history of a metabolic disorder affecting the skeletal system other than osteoarthritis or osteoporosis
5. A history of uncontrolled diabetes
6. Are unable to provide consent for the study
7. Are unable to make the follow-up appointments required of the study

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Early; Participants randomized to this arm will begin physical therapy of their fractured wrist approximately one week following surgery	Procedure: Physical therapy; Physical therapy to instruct participant with exercises to assist in return to normal activities following the healing of their wrist fracture
Other: Delayed; Participants randomized to this group will begin physical therapy of their fractured wrist approximately 6 weeks from their surgery. This is the approximate time frame in which therapy begins for patients not involved in the study. The term Delayed refers to therapy being delayed in starting from those in the study who begin therapy at one week post-operatively, not a delay in current care practice.	Procedure: Physical therapy; Physical therapy to instruct participant with exercises to assist in return to normal activities following the healing of their wrist fracture

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Range of motion measurements	at each study visit

Secondary Outcome Measures

Outcome Measure	Time Frame
Pinch strength	at each study visit
Grip strength	at each study visit
Pain	at each study visit
Return to work	at each study visit
Scores of DASH & PRWE questionnaires	at each study visit

Collaborators and Investigators

• Sponsor: Mayo Clinic
• Collaborators: DePuy Orthopaedics
• Investigators: Principal Investigator: Alexander Y. Shin, M.D., Mayo Clinic

Study record dates

Study Major Dates

• Study Start: October 1, 2006
• Primary Completion (Actual): February 1, 2010
• Study Completion (Actual): February 1, 2010

Study Registration Dates

• First Submitted: January 5, 2009
• First Submitted That Met QC Criteria: January 5, 2009
• First Posted (Estimate): January 6, 2009

Study Record Updates

• Last Update Posted (Estimate): April 8, 2011
• Last Update Submitted That Met QC Criteria: April 6, 2011
• Last Verified: April 1, 2011

More Information

Terms related to this study

• Keywords: Radius fractures
• Additional Relevant MeSH Terms: Wounds and Injuries; Arm Injuries; Forearm Injuries; Fractures, Bone; Radius Fractures
• Other Study ID Numbers: 06-004364