NCT07079202

Brief Summary

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

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 13, 2025

Completed
4 days until next milestone

Study Start

First participant enrolled

July 17, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 22, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 28, 2025

Completed
3 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2025

Completed
Last Updated

July 22, 2025

Status Verified

July 1, 2025

Enrollment Period

1 month

First QC Date

July 13, 2025

Last Update Submit

July 13, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • ELECTROMYOGRAPHIC ACTIVITY OF TRUNK MUSCLES

    6 Weeks

Secondary Outcomes (4)

  • lumbar proprioception

    6 Weeks

  • Pain intensity level

    6 weeks

  • Trunk Rang Of Motion

    6 Weeks

  • Functional disability level

    6 Weeks

Study Arms (2)

Kinetic control

EXPERIMENTAL

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.

Other: kinetic control

Conventional physical therapy

ACTIVE COMPARATOR

This group received only conventional physical therapy. ( TENS, hot backs, Ultrasound, Nerve mobilization ) three sessions per week for 6 weeks.

Other: Conventional physical therapy.

Interventions

Kinetic Control uses the Movement Control Rating System based on motor tests, the purpose of which is to identify the place and direction of uncontrolled movements and exercises to re-educate motor control

Kinetic control

This group received only conventional physical therapy. ( TENS, hot backs, Ultrasound,Nerve mobilization ) three sessions per week for 6 weeks.

Conventional physical therapy

Eligibility Criteria

Age35 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Madonna Maher Ezzat

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, CARE PROVIDER
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Teaching Assistant

Study Record Dates

First Submitted

July 13, 2025

First Posted

July 22, 2025

Study Start

July 17, 2025

Primary Completion

August 28, 2025

Study Completion

August 31, 2025

Last Updated

July 22, 2025

Record last verified: 2025-07