Mulligan Mobilization & Stretching Effects of Cervical
Effects of Mulligan Mobilization and Stretching on Cervical Radiculopathy
1 other identifier
interventional
30
1 country
1
Brief Summary
- 1.To evaluate the effectiveness of mulligan mobilization and stretching exercises in reducing pain in individuals with cervical radiculopathy.
- 2.To evaluate the effectiveness of mulligan mobilization and stretching exercises in reducing disability in individuals with cervical radiculopathy.
- 3.To evaluate the effectiveness of mulligan mobilization and stretching exercises at improving ranges in individuals with cervical radiculopathy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2025
1 active site
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
June 23, 2025
CompletedFirst Posted
Study publicly available on registry
July 1, 2025
CompletedStudy Start
First participant enrolled
July 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 30, 2026
February 25, 2026
February 1, 2026
1 year
June 23, 2025
February 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Change in Cervical Pain Intensity Measured by Numeric Pain Rating Scale (NPRS)
The NPRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable") High test-retest reliability has been observed in both literate and illiterate patients with rheumatoid arthritis (r = 0.96 and 0.95, respectively) before and after medical consultation.
4 Weeks
Cervical Range of Motion by Inclinometer
An inclinometer is a device used to measure angles. It is commonly used in physiotherapy to measure the range of motion (ROM) of joints and very similar to a goniometer. The digital inclinometer demonstrated excellent reliability (ICC=0.75-0.86), except for the right lateral flexion (ICC=0.74) and left rotation (ICC=0.72).
4 Weeks
Cervical Disability by Neck Disability Index (NDI)
This questionnaire has been designed to give us information as to how your neck pain has affected your ability to manage in everyday life. Score: /50 Transform to percentage score x 100 = %points. It has 7 items for daily living, 2 for pain and 1 for concentration. Each item is rated from 0 to 5. Total score is presented in percentage. Higher score tells greater disability while 0 means no disability(16).Total score is 50. In cervical radiculopathy patients it has moderate test retest reliability ICC= 0.68 (22).The NDI has a fair to moderate test-retest reliability in patients with mechanical neck pain but also for patients with cervical radiculopathy. The NDI has a good construct validity.
4 Weeks
Study Arms (2)
Group A-Mulligan Mobilization
EXPERIMENTALMulligan SNAGs mobilization technique was applied at level C4/5.
Group B-Stretching Exercises
EXPERIMENTALCervical stretching exercises will be performed.
Interventions
Group A will receive Mulligan mobilizations (SNAGs). Mulligan SNAGs mobilization technique was applied at level C4/5. Subjects were placed in sitting position and therapist stood behind the patient with therapist's thumbs on spinous process of particular vertebra. Mobilization was given by active movement followed by passive overpressure based on the movement restricted. The duration of treatment was three sets of ten repetitions each. Conventional treatment include the following: Subjects in both the groups were treated with hot pack (20 min), TENS (2 to 10 Hz), and manual traction along with deep neck flexor, and isometric neck strengthening.
Group B will receive stretching exercises. Subject was asked to lie supine on the plinth and the head was held at the edge of the plinth by the therapist. Then with one hand the therapist held the neck in cervical lateral flexion to the opposite side so as to achieve the stretching of the trapezius muscle. Myofascial release by applying sustained finger pressure for 5-10 s on the involved trapezius was given. A gentle myofascial stretching force was applied to take up slack and sustained until a release occurred. This protocol comprised four sets of 15 stretches with 3 min rest. Conventional treatment include the following: Subjects in both the groups were treated with hot pack (20 min), TENS (2 to 10 Hz), manual traction along with deep neck flexor, and isometric neck strengthening.
Eligibility Criteria
You may qualify if:
- Participants falling in this category would be recruited into the study.
- Both genders
- Age between 20-50 years
- Subjects with neck pain radiating down to the arm
- Patients with positive findings for spurling test, Upper Limb Tension Test (ULTT), cervical distraction test and cervical rotation test towards the symptomatic side
- Subjects who were willing to participate in the study and willing to take treatment for cervical radiculopathy.
You may not qualify if:
- Participant failing to fall in this category would be excluded of the study.
- Systemic disease potentially affecting the musculoskeletal system Patients experiencing primary shoulder or upper extremity problem of local origin
- Patients with any cardiovascular disorders and respiratory disorders
- Patients with any other pathological conditions involving cervical spine like vertebro basilar insufficiency and canal stenosis
- Patients having osteophytes in cervical vertebrae
- Patients who were undergoing treatment for neck pain with other means of physiotherapy at the time of the study
- Hypermobile joints of cervical vertebrae, Cervical fractures, spinal surgery or other spinal pathologies (i.e. ankylosing spondylitis, spondylolysthesis)
- Peripheral nerve lesions like neurotemesis and axonotemesis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Leady Reading Hospital (LRH), Hayatabad Medical Complex (HMC)
Peshawar, KPK, 25100, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ayesha Sadiq, MSPT (OMPT)
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 23, 2025
First Posted
July 1, 2025
Study Start
July 15, 2025
Primary Completion (Estimated)
July 30, 2026
Study Completion (Estimated)
December 30, 2026
Last Updated
February 25, 2026
Record last verified: 2026-02