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Integrated Rehabilitation Program for Fractures

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ClinicalTrials.gov Identifier: NCT01817933
Recruitment Status : Completed
First Posted : March 26, 2013
Last Update Posted : March 26, 2013
Sponsor:
Information provided by (Responsible Party):
Ta-Sen Wei,MD, Changhua Christian Hospital

Brief Summary:

The recovery of range of motion and muscle power after surgical intervention of the fracture will mostly affect patient's daily activities. So postoperative rehabilitation program will play the important role. Correct and effective physical therapy will reduce the functional impairment of limbs after long term casting or surgical fixation, and accelerate to recover the independent daily activities. There is no consensus between immediate or delay and the duration of continue physical therapy will improve the shoulder function、muscle power and degree of satisfaction( physiological function、social function、mental health、 pain、 general health status ) after surgical fixation of fractures. This study will evaluate the patients of the fracture that including of the humeral neck fracture, vertebral fracture, distal radial fracture and hip fractures after surgical fixation, to see the difference of fracture healing time, function recovery and pain sensation after intervention of physical therapy at different time point.

From this study, we hope to discriminate the timing of intervention and duration of physical therapy which is the key factors for postoperative prognosis of fractures fixation, and to set up the perfect rehabilitation program in ChangHua Christian Hospital. The results of this study will improve the discomfort of fracture patient's recovery or reduce the complications rate, and set up the standard treatment policy of our hospital , also was the model of other hospitals.


Condition or disease Intervention/treatment Phase
Humeral Neck Fracture Vertebral Fracture Distal Radial Fracture Hip Fractures Behavioral: physical therapy Not Applicable

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Study Type : Interventional  (Clinical Trial)
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Study Start Date : July 2010
Actual Primary Completion Date : January 2011
Actual Study Completion Date : July 2011

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Physical therapy Behavioral: physical therapy



Primary Outcome Measures :
  1. Change in pain degree [ Time Frame: 1 month after surgical fixation ]
    use Visual Analog Scale (VAS) to measure the pain condition after surgical fixation and 1 month


Secondary Outcome Measures :
  1. Change in range of motion at the fracture area [ Time Frame: 1 month after surgical fixation ]
    to access the range of motion in the elbow, wrist, hip, and knee joint, and the muscle power of upper limb and lower limb



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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • patients with humeral neck fracture, vertebral fracture, distal radial fracture or hip fractures after surgical fixation

Exclusion Criteria:

  • no
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Responsible Party: Ta-Sen Wei,MD, Director, Physical Medical and Rehabilitation, Principal Investigator, Clinical Professor, Changhua Christian Hospital
ClinicalTrials.gov Identifier: NCT01817933    
Other Study ID Numbers: CCH-100410
First Posted: March 26, 2013    Key Record Dates
Last Update Posted: March 26, 2013
Last Verified: March 2013
Additional relevant MeSH terms:
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Fractures, Bone
Hip Fractures
Spinal Fractures
Radius Fractures
Wounds and Injuries
Femoral Fractures
Hip Injuries
Leg Injuries
Spinal Injuries
Back Injuries
Forearm Injuries
Arm Injuries