NCT03838315

Brief Summary

This study will evaluate Effects of Neural Mobilization with or without Soft Tissue Mobilization in Cervical Radiculopathy, half of the subjects will receive treatment of Neural Mobilization along with Soft Tissue Mobilization whereas half of the subjects will receive only Neural Mobilization.

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
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2019

Shorter than P25 for not_applicable

Status
unknown

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

February 9, 2019

Completed
3 days until next milestone

First Posted

Study publicly available on registry

February 12, 2019

Completed
8 days until next milestone

Study Start

First participant enrolled

February 20, 2019

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 20, 2019

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 20, 2019

Completed
Last Updated

February 15, 2019

Status Verified

February 1, 2019

Enrollment Period

3 months

First QC Date

February 9, 2019

Last Update Submit

February 12, 2019

Conditions

Keywords

Cervical Radiculopathy,Neural Mobilizations,Soft Tissue Mobilization

Outcome Measures

Primary Outcomes (1)

  • Neck Pain Numeric Scale

    Pain intensity in one of the upper limb is measured by Numeric pain scale in which "0"

    4weeks

Secondary Outcomes (1)

  • Neck Disability Index

    4weeks

Study Arms (2)

Neural Mobilization with Soft Tissue Mobilization

EXPERIMENTAL

Neural Mobilization with Soft Tissue Mobilization group will be assessed by spurling's test and than will involved in treatment protocol i.e Cervical Traction, Hot packs, Neural mobilization Techniques which involve Median, Radial and Ulnar Nerve Mobilization and Post Isometric Relaxation Techniques. Frequency for Neural mobilization is 3 sets of 10 repetitions for each and duration of 15minute. Participant will be scheduled to attend 12 treatment session (3 sessions every week for 4 weeks, 40mints each session)

Other: Neural Mobilization with Soft Tissue Mobilization

Neural mobilization without Soft Tissue Mobilization

ACTIVE COMPARATOR

Neural Mobilization without Soft Tissue Mobilization group will be assessed by spurling's test and than will involved in treatment protocol i.e Cervical Traction, Hot packs, Neural Mobilization Participant will be scheduled to attend 12 treatment session (3 sessions every week for 4 weeks, 30mints each session)

Other: Neural Mobilization without Soft Tissue Mobilization

Interventions

Cervical Traction for 10mints 7%of body weight with 7 second hold time and 5 second rest time. Hot Pack for 10mints. Neural mobilization technique includes Median, Radial and Ulnar nerve mobilization. Frequency for neural mobilization is 3 sets of 10 repetitions for each and duration of 10minute. •Post isometric relaxation technique

Neural Mobilization with Soft Tissue Mobilization

Cervical Traction for 10mints 7%of body weight with 7 second hold time and 5 second rest time. * Hot Pack * Neural mobilization technique includes Median, Radial and Ulnar nerve mobilization Frequency for neural mobilization is 3 sets of 10 repetitions for each and duration of 10minute.

Neural mobilization without Soft Tissue Mobilization

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patients with age 18 to 55years
  • Patients having pain more than 3months
  • Radiating pain in one of the upper limb
  • Spurling's test positive

You may not qualify if:

  • Traumatic injury of upper limb or cervical spine
  • Vertebral artery test positive(dizziness, vomiting, diplopia, drop attacks etc)
  • Patient asymptomatic for pain but symptomatic for tingling and paraesthesia
  • Circulatory disturbance of upper extremity
  • Known history of high level of spinal cord injury and malignancy
  • Thoracic Outlet syndrome

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Radiculopathy

Condition Hierarchy (Ancestors)

Peripheral Nervous System DiseasesNeuromuscular DiseasesNervous System Diseases

Central Study Contacts

Noor Ul Ain, MPhilOPT

CONTACT

Waqar Ahmed Awan, Ph D Rehab

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Subjects will be assigned randomly into two groups: Neural Mobilization with Soft tissue mobilization and Neural mobilization without Soft tissue mobilization.A coin will be flipped at start of data collection for the first patient to be assigned odd number and included in Neural mobilization with Soft tissue mobilization group. Later on odd and even numbered subjects will be included in specific group.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Associate

Study Record Dates

First Submitted

February 9, 2019

First Posted

February 12, 2019

Study Start

February 20, 2019

Primary Completion

May 20, 2019

Study Completion

June 20, 2019

Last Updated

February 15, 2019

Record last verified: 2019-02