NCT06653543

Brief Summary

The goal of this clinical trial is to investigate the effect of Mulligan mobilization with arm movement on nerve conduction velocity in patients with unilateral cervical radiculopathy. The main questions it aims to answer are :

  1. 1.Is there a statistical significant effect of mobilization with arm movement on NCV velocity in treatment of cervical radiculopathy ?
  2. 2.Is there a statistical significant effect of mobilization with arm movement on pain level in treatment of cervical radiculopathy ?
  3. 3.Is there a statistical significant effect of mobilization with arm movement on cervical ROM in treatment of cervical radiculopathy ?
  4. 4.Is there a statistical significant effect of mobilization with arm movement on neck disability level in treatment of cervical radiculopathy ?

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
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

September 1, 2024

Completed
2 months until next milestone

First Posted

Study publicly available on registry

October 22, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

January 1, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 30, 2025

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 10, 2025

Completed
Last Updated

April 27, 2025

Status Verified

April 1, 2025

Enrollment Period

3 months

First QC Date

September 1, 2024

Last Update Submit

April 25, 2025

Conditions

Keywords

mobilizationMulligancervicalradiculopathy

Outcome Measures

Primary Outcomes (1)

  • median nerve conduction study

    using nerve conduction studies to measure the median nerve (latency, amplitude, Duration , F-wave and nerve conduction velocity of motor nerve action potentials and sensory nerve action potentials ) .

    2 weeks

Secondary Outcomes (3)

  • cervical range of motion

    2 weeks

  • pain

    2 weeks

  • neck disability level

    2 weeks

Study Arms (2)

mulligan group

EXPERIMENTAL

20 participants recieving conventional therapy in addition to mulligan mobilization with arm movement

Other: Mulligan mobilization with arm movementOther: conventional therapy of cevical radiculopathy

control group

SHAM COMPARATOR

control group that revieves only the conventional therapy

Other: conventional therapy of cevical radiculopathy

Interventions

mulligan mobilization applied on cervical spine with arm movement

mulligan group

hot pack for 10 minutes, active ranges of motion (AROMs) with 3 sets of 10 repetitions and isometrics for each movement repeated 20 times with the hold of 6 to 10 seconds in each repetition

control groupmulligan group

Eligibility Criteria

Age20 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • diagnosed with cervical radiculopathy .
  • Age group between 20-60 years
  • Unilateral radiating pain through the course of median nerve .
  • Subject having positive upper limb tension test (ULTT 1)
  • either gender male and female
  • Subjects who can understand the instructions and are willing to participate in the study.

You may not qualify if:

  • History of trauma, dislocation and subluxation of upper extremity
  • Rheumatoid Arthritis
  • Malignancy
  • Spinal canal stenosis .
  • Cervical instability/Spondylolisthesis
  • VBI (Vertebral-Basillar Insufficiency)
  • Referred pain in patients with cardiac ischemia
  • Cervical or thoracic spine surgeries .
  • systemic causes like diabetic neuropathy .
  • recent fracture or surgery in and around the shoulder .
  • carpal tunnel syndrome .
  • thoracic outlet syndrome .

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kafr El-Sheikh university

Kafr El-Sheikh Governorate, Kafr el-Sheikh Governorate, 33516, Egypt

RECRUITING

MeSH Terms

Conditions

Radiculopathy

Condition Hierarchy (Ancestors)

Peripheral Nervous System DiseasesNeuromuscular DiseasesNervous System Diseases

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
teaching assistant at the department of basic science

Study Record Dates

First Submitted

September 1, 2024

First Posted

October 22, 2024

Study Start

January 1, 2025

Primary Completion

March 30, 2025

Study Completion

August 10, 2025

Last Updated

April 27, 2025

Record last verified: 2025-04

Locations