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CompletedNCT01817933Updated Mar 26, 2013

Integrated Rehabilitation Program for Fractures

An interventional study of physical therapy in Humeral Neck Fracture, Vertebral Fracture and Distal Radial Fracture, sponsored by Changhua Christian Hospital. Completed. Per ClinicalTrials.gov, last updated 2013-03-26.

Sponsored by Changhua Christian Hospital · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Allocation
Not applicable
Sex
All
01

Study 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.

02

Conditions studied

  • Humeral Neck Fracture
  • Vertebral Fracture
  • Distal Radial Fracture
  • Hip Fractures
03

In context

Spinal Fractures

167 studies on the registry are indexed under Spinal Fractures; 29 are open to participants now.

Browse Spinal Fractures studies →

Lead sponsor

Changhua Christian Hospital is the lead sponsor of 76 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • no
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)

Study arms

  • Experimental
    Physical therapy

    Behavioral: physical therapy

Interventions

  • Behavioralphysical therapy
06

What researchers measure

Primary outcomes

  1. Change in pain degree

    use Visual Analog Scale (VAS) to measure the pain condition after surgical fixation and 1 month

    Time frame: 1 month after surgical fixation

Secondary outcomes

  1. Change in range of motion at the fracture area

    to access the range of motion in the elbow, wrist, hip, and knee joint, and the muscle power of upper limb and lower limb

    Time frame: 1 month after surgical fixation

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jul 2010, a primary completion of Jan 2011 and a completion of Jul 2011. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 20, 2013
First posted
Mar 26, 2013
Start
Jul 2010
Primary completionActual
Jan 2011
CompletionActual
Jul 2011
Last update
Mar 26, 2013
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 26, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01817933
Lead sponsor
Changhua Christian Hospital
Responsible party
Ta-Sen Wei,MD (Director, Physical Medical and Rehabilitation, Principal Investigator, Clinical Professor, Changhua Christian Hospital) — Principal investigator
First posted
Mar 26, 2013
Start date
Jul 2010
Primary completion
Jan 2011
Completion
Jul 2011
Last update
Mar 26, 2013
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2013. You cannot join it, but the record below documents what was studied.

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