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Trunk Forward Ability in Patients With Lumbar Fusion

Joint Coordination Changes During Functional Activities After Lumbar Fusion

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01585337
Enrollment
30
Registered
2012-04-25
Start date
2012-01-31
Completion date
2016-12-31
Last updated
2015-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fusion of Spine, Lumbar Region

Brief summary

The hypotheses of this study are as follows: 1. There is no significant muscle activity difference of each muscle in patients between pre and post operation. 2. There is no significant forward reach distance/average velocity difference in patients between pre and post operation. 3. There is no significant standard deviation of center of pressure (COP) along x axis, speed of COP along y axis during the task and COP path during the 3-sec holding phase difference in patients between pre and post operation. 4. There is no significant muscle activity difference between muscles on both sides at post operation.

Detailed description

30 healthy adults and 30 patients is going to undergo lumbar fusion surgery will be recruited in this study. The assessment will be held before surgery, two months, three months and six months after surgery. Visual pain scale and passive range of motion over lumbar, hip, knee, ankle joint of each subjects will be recorded. Then the maximum voluntary contraction at lower extremity will be measured by electromyography. Finally, the subjects will be asked to do forward reach by dominant upper limb/bilateral upper limbs/arm crossed in the front of chest for three times in standing and sitting position after five practices. The motion data will be collected by 3-dimension video and the muscle activity by electromyography.

Interventions

None listed

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. specific low back pain with MRI finding by the radiologist and the surgeon; 2. patient who is scheduled for MISS in one week.

Exclusion criteria

1. scoliosis; 2. neurological disorder; 3. Self-reported impairment in daily activities; 4. leg length deficiency over 2 cm; 5. body mass index over 30.

Design outcomes

Primary

MeasureTime frame
EMGone months post operation

Secondary

MeasureTime frame
forward reach distanceone month post operation

Countries

Taiwan

Contacts

Primary ContactWei-Li Hsu, PhD
wlhsu@ntu.edu.tw+8862-33668127

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026