Integrated Rehabilitation Program for Fractures
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| ClinicalTrials.gov Identifier: NCT01817933 |
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Recruitment Status :
Completed
First Posted : March 26, 2013
Last Update Posted : March 26, 2013
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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 |
| 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 |
| Arm | Intervention/treatment |
|---|---|
| Experimental: Physical therapy |
Behavioral: physical therapy |
- 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
- 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 |
Inclusion Criteria:
- patients with humeral neck fracture, vertebral fracture, distal radial fracture or hip fractures after surgical fixation
Exclusion Criteria:
- no
| 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 |
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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 |

