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Cervical RadiculopathyNCT03838315

Effects of Neural Mobilization With or Without Soft Tissue Mobilization in Cervical Radiculopathy

A study testing Neural Mobilization with Soft Tissue Mobilization and Neural Mobilization without Soft Tissue Mobilization in people with Cervical Radiculopathy, run by Isra University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 55 years
Conditions the study is for
Cervical Radiculopathy
What is being tested?
Neural Mobilization with Soft Tissue Mobilization and Neural Mobilization without Soft Tissue Mobilization
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
No sites listed yet
Study dates
20 Feb 2019to 20 Jun 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 55 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

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

Who cannot join

  • 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

Trial locations and contacts

No sites are listed yet.

Noor Ul Ain, MPhilOPT contact

0333-5292822

Noorabid2015@gmail.com

Waqar Ahmed Awan, Ph D Rehab contact

03335348846

wawan01@hotmail.com

About this study

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.

Read the detailed description

Neural mobilization and Soft Tissue Mobilization both treatments are used to treat Cervical Radiculopathy but they work differently.

Neural mobilization technique is different for all 3 nerves i.e Radial, ulnar and median. Neural Mobilization Technique target the single nerve which is being compressed and showing symptoms.

Soft Tissue Mobilization include traction which decompresses the nerve and stretches the surrounding muscles along with help to reduce pain and tingling sensation. whereas hot pack helps to increase blood circulation and warm up muscles and isometric exercises provide strengthening and build endurance.

Being tested
Neural Mobilization with Soft Tissue Mobilization, Neural Mobilization without Soft Tissue Mobilization
Keywords
Cervical Radiculopathy,, Neural Mobilizations,, Soft Tissue Mobilization
Medical subject headings
Radiculopathy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Neural Mobilization with Soft Tissue MobilizationOther

    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 without Soft Tissue MobilizationOther

    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.
Study groups in NCT03838315
Study groupRoleWhat they receive
Neural Mobilization with Soft Tissue MobilizationExperimentalNeural 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)
Receives: Other: Neural Mobilization with Soft Tissue Mobilization
Neural mobilization without Soft Tissue MobilizationActive comparatorNeural 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)
Receives: Other: Neural Mobilization without Soft Tissue Mobilization

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Neck Pain Numeric Scale

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

    Measured: 4weeks

Secondary outcomes (1)
  1. Neck Disability Index

    Neck disability index scale used to measure ability to manage neck pain in everyday life in terms of: Pain intensity, Personal care, Lifting, Reading, Headaches, and Concentration. In which "0" shows disability and "5" shows normal.

    Measured: 4weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Feb 2019
  2. Study start20 Feb 2019 (estimated)
  3. Primary completion20 May 2019 (estimated)
  4. Study completion20 Jun 2019 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
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.
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03838315
Sponsor's protocol ID
IIRS-IUISB/MphilOPT/002
Status last verified
Feb 2019
First submitted
9 Feb 2019
Last updated
15 Feb 2019
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Neural Mobilization with Soft Tissue Mobilization and Neural Mobilization without Soft Tissue Mobilization in people with Cervical Radiculopathy, run by Isra University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 15 Feb 2019. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Noor Ul Ain, MPhilOPT (0333-5292822, Noorabid2015@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Neck Pain Numeric Scale (time frame: 4weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Feb 2019.

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