Effects of Multimodal Physical Therapy in Patients With Lumbosacral Radiculopathy

NCT ID: NCT06058806

Last Updated: 2023-09-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

14 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-06-01

Study Completion Date

2020-01-20

Brief Summary

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Purposes of the study

To investigate the effect of Multimodal Physical Therapy on pain, daiablility H-reflex, and Diffusion Tensor Imaging (DTI) Parameters in Patients With Lumbosacral Radiculopathy.

Detailed Description

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Participants will receive Multimodal Physical Therapy program consisting of electrophysical agents, manual therapy interventions, and core stability exercises. Patients will receive the intervention for six weeks. Outcomes will be assessed at baseline and post-intervention.

Conditions

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Lumbosacral Radiculopathy

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Multimodal Physical Therapy

Patients in this group will receive Multimodal Physical Therapy program consisting of electrophysical agents, manual therapy interventions, and core stability exercises.

Group Type EXPERIMENTAL

Multimodal Physical Therapy

Intervention Type OTHER

Multimodal Physical Therapy program consisting of electrophysical agents, manual therapy interventions, and core stability exercises

Interventions

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Multimodal Physical Therapy

Multimodal Physical Therapy program consisting of electrophysical agents, manual therapy interventions, and core stability exercises

Intervention Type OTHER

Other Intervention Names

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Physical Therapy Physiotherapy

Eligibility Criteria

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Inclusion Criteria

* chronic (≥ 3 months) unilateral Lumbosacral Radiculopathy (LSR)
* The LSR is due to paracentral L4-L5 or L5-S1 Lumbar disc herniation
* The LSR is confirmed radiologically by MRI
* The LSR is confirmed clinically by history and physical examination
* The LSR is confirmed neurophysiological by soleus H-reflex assessment
* Body mass Index less than 30
* 20-45 years of age

Exclusion Criteria

* systematic disease
* Bilateral symptoms
* Lumbar spinal stenosis
* previous surgery
* Steroid injection
* Spinal fracture
* Lumbar spinal stenosis
* Spinal deformity
* Spinal fracture
* Radiological evidence of bilateral nerve root encroachmen
* Evidence of H-reflex amplitude or latency affection on asymptomatic side
Minimum Eligible Age

20 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Mohamed Badr Hassanein

Mr

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Outpatient clinic, Faculty of Physical Therapy, Cairo University

Giza, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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MBH18

Identifier Type: -

Identifier Source: org_study_id

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