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Effect of Kinetic Control in Lumbosacral Radiculopathy. (KC)

M

Madonna Maher Ezzat Yassa

Status

Not yet enrolling

Conditions

Chronic Low Back Pain
LUMBOSACRAL RADICULOPATHY

Treatments

Other: Conventional physical therapy.
Other: kinetic control

Study type

Interventional

Funder types

Other

Identifiers

NCT07079202
P.T.REC/012/004918

Details and patient eligibility

About

-This study would answer the following question: Is there an effect of kinetic control retraining on electromyographic activity of trunk and lumbar proprioception in patients with lumbosacral radiculopathy?

The aims of this study are:

  1. To investigate the effect of kinetic control retraining on electromyographic activity of trunk in patients with lumbosacral radiculopathy
  2. To investigate the effect of kinetic control retraining on lumbar proprioception in patients with lumbosacral radiculopathy.
  3. To investigate the effect of kinetic control retraining on trunk Range of motion (ROM) in patients with lumbosacral radiculopathy.
  4. To investigate the effect of kinetic control retraining on pain intensity in patients with lumbosacral radiculopathy. 5 -To investigate the effect of kinetic control retraining on functional disability in patients with lumbosacral radiculopathy.

Enrollment

50 estimated patients

Sex

All

Ages

35 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients will be from both sexes.
  2. The age of patients will range from 35- 50 years old.
  3. The Body Mass Index (BMI) of patients will be less than 30Kg/m2
  4. All patients represent chronic low back pain (at least 3 months).
  5. Patients with unilateral lumbosacral radiculopathy (L4-5, L5-S1) due to Posterolateral disc prolapse.
  6. Patients have been diagnosed by MRI.
  7. Patients with sufficient cognitive abilities that enables them to understand and follow instructions (Mini-Mental State Examination (MMSE) scale >24).

Exclusion criteria

  1. Previous spinal surgeries
  2. Another Causes of the lumbosacral radiculopathy
  3. Pain that persists less than 3 months
  4. Spinal tumors
  5. Lumbar instability due to structural problems, for example: ligament tear or spondylolythesis.
  6. Cognitive impairment (a score less than 24 according to MMSE).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups

Kinetic control
Experimental group
Description:
This group received kinetic control retraining protocol in addition to conventional physical therapy. ( TENS, hot backs, Ultrasound,Nerve mobilization ) three sessions per week for 6 weeks.
Treatment:
Other: kinetic control
Conventional physical therapy
Active Comparator group
Description:
This group received only conventional physical therapy. ( TENS, hot backs, Ultrasound, Nerve mobilization ) three sessions per week for 6 weeks.
Treatment:
Other: Conventional physical therapy.

Trial contacts and locations

0

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Central trial contact

Madonna Maher Ezzat

Data sourced from clinicaltrials.gov

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