Cervical RadiculopathyNCT05959330
Effects of Neural Tension Versus Neural Sliding Technique on Cervical Radiculopathy.
A study testing Neural Tension Technique(ulnar, median, radial), Neural Slider Technique (ulnar, median, radial) and Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial) in people with Cervical Radiculopathy, run by Riphah International University at 1 site in Pakistan.
Trial summary
The aim of this research is to find the effects of neural tension versus neural sliding technique on pain, cervical muscle endurance and hand grip strength in unilateral cervical radiculopathy. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Cervical Radiculopathy
- What is being tested?
- Neural Tension Technique(ulnar, median, radial), Neural Slider Technique (ulnar, median, radial) and Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 1 sitePakistan
- Study dates
- 5 Mar 2023to 30 Jul 2023
- 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 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- • Unilateral radicular pain in upper limb since 3 months(10)
- Any two of the following tests positive: Spurling's test, Distraction test, Upper Limb Tension Test
Who cannot join
- • Any orthopedic or neurological conditions of cervical spine and shoulder joint
- Hypermobility of cervical spine
- Malignancy
- Vertebro-basilar insufficiency
- Patients undergone cervical surgeries
- Patients with bilateral cervical radiculopathies
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effects of Neural Tension Versus Neural Sliding Technique on Pain, Cervical Muscle Endurance and Hand Grip Strength in Unilateral Cervical Radiculopathy
The aim of this research is to find the effects of neural tension versus neural sliding technique on pain, cervical muscle endurance and hand grip strength in unilateral cervical radiculopathy. It will be a randomized controlled trial in which participants selected through non probability convenience sampling with age from 18 to 65 years having unilateral cervical radicular pain in upper limb since 3 months and any two of the following positive test Spurling's test, Distraction test and Upper Limb Tension Test. Participants will be randomly allocated, into three groups (A, B, and C). On the contrary, patients with any orthopedic or neurological conditions of cervical spine and shoulder joint, malignancy, cervical surgeries and bilateral cervical radiculopathies will be excluded from the study. Baseline measurement of all groups will be taken by using Numerical Pain Rating Scale (NPRS) for pain, Cranio-cervical Flexion Test for endurance and Hand-Held Dynamometer for hand grip strength. Group A will receive 7 neural tension technique, Group B will receive neural sliding technique, while Group C will receive both neural tension technique and neural sliding technique for 4 weeks (6 successive sessions). Both techniques (slider and tensioner) will be provided three sets in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment. SPSS 21 software will be used for data entry and analysis.
Read the detailed description
Cervical radiculopathy also known as "pinched nerve", is a neurological condition caused by compression of the cervical spine nerve and roots. It is basically a lower motor neuron and sensory demonstration of neurological dysfunction of the involved cervical nerve root. Cervical radiculopathy is most commonly caused by the herniation of the cervical spine intervertebral disc or any space-occupying lesion that may lead to nerve root inflammation or impingement. Other common causes of cervical radiculopathy are spondylosis, trauma, osteoporosis, cervical instability, and sometimes oncological issues. Such problems either directly compress the cervical nerve roots or narrow the space of the vertebral foramen from where the cervical nerve root emerges which leads to neuritis, hypoxia, ischemia, fibrosis, edema, or decreased nerve mobility. Cervical radiculopathy has an average annual incident rate of 83 per 100,000 of the population with an increased prevalence in the fourth and fifth decade of life.
According to studies, the most commonly affected cervical nerve root is C7 followed by the C6 and C8. The clinical manifestation of cervical radiculopathy is quite broad involving motor and sensory changes in the upper extremity. Patients with cervical radiculopathy usually experience loss of sensation, tingling, numbness, motor defects in the neck and sometimes in the scapula, and pain in the arm and hand along the pathway of the nerve depending upon the location of the affected nerve root. The pain can be radiated both bilaterally and unilaterally into the arms, however, the prevalence of bilateral cervical radiculopathy is only 5 - 36%.
The symptoms of muscle weakness in the upper limb are often seen in patients with cervical radiculopathy. According to the principles of the kinetic chain, the upper limb is an integrated system consisting of different segments working together to accomplish the activities of daily living. In simpler words, the muscle weakness produced in any segment of the upper limb would result in generalized muscle weakness and ultimately decreased hand grip strength. To perform functional activities of daily living it is very important to maintain the grip strength of the upper extremity. But, to achieve the maximum grip strength the physical and physiological properties of nerve tissues need to be intact. Since reduced grip strength is often seen in patients with cervical radiculopathy, it becomes essential to administer an appropriate technique to rehabilitate its strength
Manual therapy techniques are considered effective in the treatment of cervical radiculopathy. Neurodynamic mobilization has been considered effective as a conservative management approach for the treatment of upper quadrant pain. It restores homeostasis in and around the neural tissues by improving the mechanical and neurophysiological integrity of the peripheral nerves, thus reducing pain and disability. Slider and tensioner are the two most commonly used neural mobilization techniques and a biomechanical distinction can be made between these two techniques. Neural mobilization plays an important role in returning to normal functional activities by restoring the range of motion and extensibility of the nervous system
Neurodynamic mobilization restores the neural tissues' ability to resist tension and stress by promoting the restoration of normal physiological function, decreasing pain, and improving function. The slider neurodynamic mobilization causes sliding movement in the neural tissue in correspondence to the nearby structures; distributing the compression and tension along the entire nervous instead of one particular region. On the other hand, tensioner neurodynamic mobilization causes tension in the neural tissue without surpassing the tissue elastic capacity that enhances nerve's viscoelastic properties. This procedure is done by taking the nerve, in the end, range of movement (elongated position), maintaining the position for a short duration, and then fully releasing the tension.
A systematic review of a randomized control trial was done by Papacharalambous C et al. in 2022 to evaluate the effectiveness of slider and tensioner neural mobilization techniques in the management of upper quadrant pain. The results of the study concluded that slider and tensioner neural mobilization techniques are quite effective in reducing pain in certain musculoskeletal conditions. Moreover, the results revealed that slider neural mobilization technique is more effective in the treatment of acute conditions than tensioner neural mobilization.
A randomized clinical trial was conducted by Shou MK et al. in 2022, to determine the effects of neural slider and contralateral cervical lateral glide in athletes with cervicobrachial pain syndrome. Thirty patients were recruited in the study that were divided into groups. One group received neural slider technique whereas the other received contralateral cervical lateral glide. The results revealed that both techniques are effective in improving pain and functional disability. However, the contralateral cervical lateral glide is more effective than the neural mobilization technique for patients with cervicobrachial pain syndrome.
Raval MM et al. conducted a comparative study in 2022 to determine the effect of neural sliding technique versus neural sliding technique on functional disability and pain in patients with cervical radiculopathy. A total of thirty patients were recruited for the study and later divided into two equal groups. Group A received neural tension mobilization while Group B received neural sliding mobilization. Outcome measure tools Numeric Pain Rating Scale, Neck Disability Index, and Patient Specific Functional Scale were used to access the patient before and after the treatment. The results of the study concluded that tensioner neurodynamic mobilization is more effective in reducing functional disability and pain than slider neurodynamic mobilization.
- Conditions
- Cervical Radiculopathy
- Being tested
- Neural Tension Technique(ulnar, median, radial), Neural Slider Technique (ulnar, median, radial), Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial)
- Keywords
- Slider, Tensioner Neurodynamic Mobilization, Cervical Radiculopathy, Hand Grip Strength, Numeric Pain Rating Scale
- Medical subject headings
- Radiculopathy
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Neural Tension Technique(ulnar, median, radial)Other
Neural Tension Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment
Neural Slider Technique (ulnar, median, radial)Other
Neural Slider Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment
Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial)Other
Neural Tension and Sliding Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment
| Study group | Role | What they receive |
|---|---|---|
| Neural Tension Technique(ulnar, median, radial) | Experimental | Neural Tension Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment Receives: Other: Neural Tension Technique(ulnar, median, radial) |
| Neural Slider Technique (ulnar, median, radial) | Experimental | Neural Slider Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment Receives: Other: Neural Slider Technique (ulnar, median, radial) |
| Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial) | Experimental | Neural Tension and Sliding Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment Receives: Other: Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Numeric Pain Rating Scale
Numeric Pain Rating Scale is a subjective outcome measure tool that is used to measure intensity of pain in adults. It is a numeric version of Visual Analogue Scale. NPRS is a unidirectional 11- point scale that ranges from 0 to 10. With "0" indicating the 'no pain at all' and "10" indicating the 'the worst pain imaginable'. The NPRS can be administered either graphically or verbally. The respondent is asked to indicate the numeric value that describes their current pain intensity best
Measured: Changes from baseline Numeric Pain Rating Scale (NPRS) at 1 months
Hand-Held Dynamometer
The patient will be asked to sit on a straight back chair with his/her feet flat on the floor. The affected shoulder was to be maintained at 0º of flexion, abduction and rotation, elbow flexed to 90º, forearm rested in a neutral position with the wrist in minimal extension and ulnar deviation.
On achieving the standardized arm position, the dynamometer set at the second handle space was given to subjects who were then advised to perform 3 maximum gripping efforts for 5 seconds. A 15 second rest period was given to prevent fatigue effects.
While performing each trial, each patient was instructed by the assessor as follows: "Squeeze the handle as hard as possible". The mean value of the 3 efforts (measured in pounds) was evaluated for the analysis of grip strength. The patients were not allowed to see their score in each trial. No visual and verbal encouragement was given for achieving the maxi-mum capable grip strength
Measured: Changes from baseline Hand-Held Dynamometer (HHD) at 1 months
Cervico-cranial Flexion Test (Blood Pressure Cuff)
A blood pressure cuff is inflated to 20 mmHg and is placed between the lordotic curve and the surface of the table. While keeping the back of the head stable, the patient performs cranial cervical flexion in a graded fashion in 5 increments (22, 24, 26, 28, and 30 mmHg). Each position is held for 10 seconds with 10 seconds rest between increments. The cranial cervical flexion is performed by a head nod in the upper cervical spine. Make sure the patient's jaw is relaxed, so that there is no platysma, hyoid muscle, or sternocleidomastoid recruitment.
The test is ended when the pressure decreases >20% or when substitution occurs during the head nod. Normal response is achieving 26-30 mmHg.[
Measured: Changes from baseline Cervico-cranial Flexion Test (CCFT) at 1 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Jul 2023
- Study start5 Mar 2023
- Primary completion15 Jul 2023
- Study completion30 Jul 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Cervical RadiculopathyStudies of the same condition, open and under way.
- More trials run by Riphah International UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- Riphah International University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Sehar Fatima, DPT, Principal investigator, Riphah International University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05959330
- Sponsor's protocol ID
- RiphahIU Sehar Fatima
- Status last verified
- Dec 2023
- First submitted
- 31 Mar 2023
- Last updated
- 27 Dec 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Kang KC, Lee HS, Lee JH. Cervical Radiculopathy Focus on Characteristics and Differential Diagnosis. Asian Spine J. 2020 Dec;14(6):921-930. doi: 10.31616/asj.2020.0647. Epub 2020 Dec 22.
PubMed 33373515
Study at a glance
From the registry record, last updated by the sponsor on 27 Dec 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Neural Tension Versus Neural Sliding Technique on Pain, Cervical Muscle Endurance and Hand Grip Strength in Unilateral Cervical Radiculopathy
- ClinicalTrials.gov ID
- NCT05959330
- Acronym / sponsor ID
- RiphahIU Sehar Fatima
- Conditions
- Cervical Radiculopathy
- Keywords
- Slider, Tensioner Neurodynamic Mobilization, Cervical Radiculopathy, Hand Grip Strength, Numeric Pain Rating Scale
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- Riphah International UniversityUniversity, hospital or other
- Study start
- 5 Mar 2023 (actual)
- Primary completion
- 15 Jul 2023 (actual)
- Study completion
- 30 Jul 2023 (actual)
- First posted
- 25 Jul 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this research is to find the effects of neural tension versus neural sliding technique on pain, cervical muscle endurance and hand grip strength in unilateral cervical radiculopathy. It will be a randomized controlled trial in which participants selected through non probability convenience sampling with age from 18 to 65 years having unilateral cervical radicular pain in upper limb since 3 months and any two of the following positive test Spurling's test, Distraction test and Upper Limb Tension Test. Participants will be randomly allocated, into three groups (A, B, and C). On the contrary, patients with any orthopedic or neurological conditions of cervical spine and shoulder joint, malignancy, cervical surgeries and bilateral cervical radiculopathies will be excluded from the study. Baseline measurement of all groups will be taken by using Numerical Pain Rating Scale (NPRS) for pain, Cranio-cervical Flexion Test for endurance and Hand-Held Dynamometer for hand grip strength. Group A will receive 7 neural tension technique, Group B will receive neural sliding technique, while Group C will receive both neural tension technique and neural sliding technique for 4 weeks (6 successive sessions). Both techniques (slider and tensioner) will be provided three sets in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment. SPSS 21 software will be used for data entry and analysis.
Detailed description
Cervical radiculopathy also known as "pinched nerve", is a neurological condition caused by compression of the cervical spine nerve and roots. It is basically a lower motor neuron and sensory demonstration of neurological dysfunction of the involved cervical nerve root. Cervical radiculopathy is most commonly caused by the herniation of the cervical spine intervertebral disc or any space-occupying lesion that may lead to nerve root inflammation or impingement. Other common causes of cervical radiculopathy are spondylosis, trauma, osteoporosis, cervical instability, and sometimes oncological issues. Such problems either directly compress the cervical nerve roots or narrow the space of the vertebral foramen from where the cervical nerve root emerges which leads to neuritis, hypoxia, ischemia, fibrosis, edema, or decreased nerve mobility. Cervical radiculopathy has an average annual incident rate of 83 per 100,000 of the population with an increased prevalence in the fourth and fifth decade of life.
According to studies, the most commonly affected cervical nerve root is C7 followed by the C6 and C8. The clinical manifestation of cervical radiculopathy is quite broad involving motor and sensory changes in the upper extremity. Patients with cervical radiculopathy usually experience loss of sensation, tingling, numbness, motor defects in the neck and sometimes in the scapula, and pain in the arm and hand along the pathway of the nerve depending upon the location of the affected nerve root. The pain can be radiated both bilaterally and unilaterally into the arms, however, the prevalence of bilateral cervical radiculopathy is only 5 - 36%.
The symptoms of muscle weakness in the upper limb are often seen in patients with cervical radiculopathy. According to the principles of the kinetic chain, the upper limb is an integrated system consisting of different segments working together to accomplish the activities of daily living. In simpler words, the muscle weakness produced in any segment of the upper limb would result in generalized muscle weakness and ultimately decreased hand grip strength. To perform functional activities of daily living it is very important to maintain the grip strength of the upper extremity. But, to achieve the maximum grip strength the physical and physiological properties of nerve tissues need to be intact. Since reduced grip strength is often seen in patients with cervical radiculopathy, it becomes essential to administer an appropriate technique to rehabilitate its strength
Manual therapy techniques are considered effective in the treatment of cervical radiculopathy. Neurodynamic mobilization has been considered effective as a conservative management approach for the treatment of upper quadrant pain. It restores homeostasis in and around the neural tissues by improving the mechanical and neurophysiological integrity of the peripheral nerves, thus reducing pain and disability. Slider and tensioner are the two most commonly used neural mobilization techniques and a biomechanical distinction can be made between these two techniques. Neural mobilization plays an important role in returning to normal functional activities by restoring the range of motion and extensibility of the nervous system
Neurodynamic mobilization restores the neural tissues' ability to resist tension and stress by promoting the restoration of normal physiological function, decreasing pain, and improving function. The slider neurodynamic mobilization causes sliding movement in the neural tissue in correspondence to the nearby structures; distributing the compression and tension along the entire nervous instead of one particular region. On the other hand, tensioner neurodynamic mobilization causes tension in the neural tissue without surpassing the tissue elastic capacity that enhances nerve's viscoelastic properties. This procedure is done by taking the nerve, in the end, range of movement (elongated position), maintaining the position for a short duration, and then fully releasing the tension.
A systematic review of a randomized control trial was done by Papacharalambous C et al. in 2022 to evaluate the effectiveness of slider and tensioner neural mobilization techniques in the management of upper quadrant pain. The results of the study concluded that slider and tensioner neural mobilization techniques are quite effective in reducing pain in certain musculoskeletal conditions. Moreover, the results revealed that slider neural mobilization technique is more effective in the treatment of acute conditions than tensioner neural mobilization.
A randomized clinical trial was conducted by Shou MK et al. in 2022, to determine the effects of neural slider and contralateral cervical lateral glide in athletes with cervicobrachial pain syndrome. Thirty patients were recruited in the study that were divided into groups. One group received neural slider technique whereas the other received contralateral cervical lateral glide. The results revealed that both techniques are effective in improving pain and functional disability. However, the contralateral cervical lateral glide is more effective than the neural mobilization technique for patients with cervicobrachial pain syndrome.
Raval MM et al. conducted a comparative study in 2022 to determine the effect of neural sliding technique versus neural sliding technique on functional disability and pain in patients with cervical radiculopathy. A total of thirty patients were recruited for the study and later divided into two equal groups. Group A received neural tension mobilization while Group B received neural sliding mobilization. Outcome measure tools Numeric Pain Rating Scale, Neck Disability Index, and Patient Specific Functional Scale were used to access the patient before and after the treatment. The results of the study concluded that tensioner neurodynamic mobilization is more effective in reducing functional disability and pain than slider neurodynamic mobilization.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Neural Tension Technique(ulnar, median, radial) | Experimental | Other: Neural Tension Technique(ulnar, median, radial)Neural Tension Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment |
| Neural Slider Technique (ulnar, median, radial) | Experimental | Other: Neural Slider Technique (ulnar, median, radial)Neural Slider Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment |
| Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial) | Experimental | Other: Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial)Neural Tension and Sliding Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- • Unilateral radicular pain in upper limb since 3 months(10)
Key exclusion criteria (6 listed)
- • Any orthopedic or neurological conditions of cervical spine and shoulder joint
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Neural Tension Technique(ulnar, median, radial)Neural Tension Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment | Other | Neural Tension Technique(ulnar, median, radial) |
| Neural Slider Technique (ulnar, median, radial)Neural Slider Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment | Other | Neural Slider Technique (ulnar, median, radial) |
| Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial)Neural Tension and Sliding Technique for 4 weeks (6 successive sessions). Three sets will be provided in every session; Each set will be performed in a slow, oscillatory manner with 10 seconds rest between the sets. Posttest measurement will be taken after 4 weeks of treatment | Other | Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial) |
Primary outcome
Numeric Pain Rating Scale
Time frame: Changes from baseline Numeric Pain Rating Scale (NPRS) at 1 months
Numeric Pain Rating Scale is a subjective outcome measure tool that is used to measure intensity of pain in adults. It is a numeric version of Visual Analogue Scale. NPRS is a unidirectional 11- point scale that ranges from 0 to 10. With "0" indicating the 'no pain at all' and "10" indicating the 'the worst pain imaginable'. The NPRS can be administered either graphically or verbally. The respondent is asked to indicate the numeric value that describes their current pain intensity best
Hand-Held Dynamometer
Time frame: Changes from baseline Hand-Held Dynamometer (HHD) at 1 months
The patient will be asked to sit on a straight back chair with his/her feet flat on the floor. The affected shoulder was to be maintained at 0º of flexion, abduction and rotation, elbow flexed to 90º, forearm rested in a neutral position with the wrist in minimal extension and ulnar deviation. On achieving the standardized arm position, the dynamometer set at the second handle space was given to subjects who were then advised to perform 3 maximum gripping efforts for 5 seconds. A 15 second rest period was given to prevent fatigue effects. While performing each trial, each patient was instructed by the assessor as follows: "Squeeze the handle as hard as possible". The mean value of the 3 efforts (measured in pounds) was evaluated for the analysis of grip strength. The patients were not allowed to see their score in each trial. No visual and verbal encouragement was given for achieving the maxi-mum capable grip strength
Cervico-cranial Flexion Test (Blood Pressure Cuff)
Time frame: Changes from baseline Cervico-cranial Flexion Test (CCFT) at 1 months
A blood pressure cuff is inflated to 20 mmHg and is placed between the lordotic curve and the surface of the table. While keeping the back of the head stable, the patient performs cranial cervical flexion in a graded fashion in 5 increments (22, 24, 26, 28, and 30 mmHg). Each position is held for 10 seconds with 10 seconds rest between increments. The cranial cervical flexion is performed by a head nod in the upper cervical spine. Make sure the patient's jaw is relaxed, so that there is no platysma, hyoid muscle, or sternocleidomastoid recruitment. The test is ended when the pressure decreases >20% or when substitution occurs during the head nod. Normal response is achieving 26-30 mmHg.[
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Dec 2023.
- Background: PubMed 33373515Kang KC, Lee HS, Lee JH. Cervical Radiculopathy Focus on Characteristics and Differential Diagnosis. Asian Spine J. 2020 Dec;14(6):921-930. doi: 10.31616/asj.2020.0647. Epub 2020 Dec 22.
- Individual participant dataSharing planned: No
Related trials for Cervical Radiculopathy
Recruiting
Ultrasound-Guided Electrical Dry Needling for Chronic Cervical Radiculopathy
Cervical Radiculopathy
Not yet recruitingObservational study
Correlation Between Forward Head Posture and Executive Functions in Cervical Radiculopathy
Cervical Radiculopathy, Forward Head Posture
Recruiting
Myo-Electrical and Nerve Root Function Response to Focused Extracorpeal Shock Wave in Cervical Radiculopathy
Cervical Radiculopathy
Not yet recruiting
Endoscopic Posterior Cervical Foraminotomy Versus Anterior Cervical Discectomy and Fusion for Cervical Radiculopathy
Cervical Disc Herniation, Cervical Foraminal Stenosis
RecruitingObservational study
Cervical Spinal Cord Signal Abnormalities in Patients With Cervical Radicular Pain
Cervical Radiculopathy, Cervical Myelomalacia
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Sehar Fatima, DPT principal investigator
Riphah International University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Neural Tension Technique(ulnar, median, radial), Neural Slider Technique (ulnar, median, radial) and Neural Tension Technique and Neural Sliding Technique(ulnar, median, radial) in people with Cervical Radiculopathy, run by Riphah International University at 1 site in Pakistan.
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 2 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: finished, as of the sponsor's last update on 27 Dec 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Numeric Pain Rating Scale (time frame: Changes from baseline Numeric Pain Rating Scale (NPRS) at 1 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05959330, which also lists 1 linked publication.
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 27 Dec 2023.