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Not yet recruitingNCT07912112Updated Nov 3, 2026

Effects of Muscle Energy Technique With and Without Scapulothoracic Mobilization on Neck Pain in Students

An interventional study of Muscle Energy Technique + Scapulothoracic Mobilization. and Muscle Energy Technique. in Non Psecific Neck Pain, sponsored by University of Management and Technology Lahore. Not yet recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 30 Years. Per ClinicalTrials.gov, last updated 2026-11-03.

Sponsored by University of Management and Technology Lahore · Not applicable, Interventional, and Treatment

Updated Nov 3, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

Non-specific neck pain is neck pain that cannot be attributed to any known, specific pathology such as inflammatory disease, cancer, fracture or infection. Non-specific neck pain accounts for a large proportion of musculoskeletal disorders among young people, especially university students, due to prolonged static postures, prolonged screen time and poor ergonomic habits. In some cases, muscular imbalances or excessive activity of the cervical and periscapular muscles due to prolonged forward head posture is suggested to be the cause. In other cases, altered neuromuscular function, limited movement of the scapulothoracic region resulting in altered cervical mechanics or mild dysfunction of the facet joints between cervical vertebrae may be the cause. In addition to these, there may be other minor disorders that cause pain and impairment of function in the connective tissues and surrounding soft tissue components in the neck and upper thorax. When symptoms last longer than three months, the term "chronic" non-specific neck pain is used.

Non-specific neck pain has been treated with numerous therapeutic interventions such as manual therapy, exercise based approaches, dry needling, postural correction and soft tissue procedures. Muscle Energy Technique (MET) is an active osteopathic manual therapies method that uses the patient's own contractions to lengthen and relax hypertonic muscles and improve joint mobility. The purpose of this study is to compare the effects of Muscle Energy Technique with and without Scapulothoracic Mobilization on pain, range of motion and disability among university students with non-specific neck pain. The study design will be a randomized clinical trial and evaluation will be done using Numeric Pain Rating Scale (NPRS), Neck Disability Index (NDI) and Goniometer. However, the most effective combination of these interventions as a method of rehabilitation for altered cervical kinematics and pain. Further research is necessary to determine the best effective mix of these interventions as a rehabilitation strategy for non-specific neck pain in college students, which reflects the complexity of the condition. This study aims to assess the response of university students with non-specific neck pain to Muscle Energy Technique with and without Scapulothoracic Mobilization in terms of pain, range of motion and impairment. A randomized clinical trial will be used as the study design. The Neck Disability Index (NDI), Goniometer and Numeric Pain Rating Scale (NPRS) will be used for evaluation. The subjects will be divided into two groups at random using non-probability convenient sampling; Group A will receive Muscle Energy Technique in addition to Scapulothoracic Mobilizations, while Group B will receive Muscle Energy Technique alone. Prior to the application of the technique, both groups will receive a 15-minute moist heat as a basic treatment for non-specific neck pain; both groups will receive 12 sessions over the course of four weeks; measurements of all outcome variables will be taken at baseline, the second week, and the fourth week. The results will be analyzed using SPSS 24.

02

Conditions studied

  • Non Psecific Neck Pain

Keywords

  • Nonspecific neck pain, Scapulothoracic mobilization, Muscle energy technique, students.
03

In context

Lead sponsor

University of Management and Technology Lahore is the lead sponsor of 34 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • University students(16)
  • 18 to 30-year-old male and female.(7)(21)(16)
  • The clinical diagnosis of non-specific neck pain.(27)
  • Lasts for at least 6 to 12 weeks, and has no obvious specific pathology.(21)
  • At the time of enrolment, a neck pain level of four or higher on the Numeric Pain Rating Scale (NPRS).(8)

Exclusion criteria

Exclusion Criteria:

  • Cervical radiculopathy or myelopathy.(27)
  • Previous cervical spine and shoulder trauma or surgery(27).
  • Diagnosed systemic or serious pathology, including malignancy, infection, inflammatory arthritis (12)
  • Participation in any structured physical therapy for neck pain within the preceding 6 months.(27)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Muscle Energy Technique + Scapulothoracic Mobilization.

    will undergo scapulothoracic mobilization after receiving Muscle Energy Technique (MET) that targets the levator scapulae and upper trapezius muscles. The therapist will position the cervical spine in flexion, contralateral side bending, and minor ipsilateral rotation for the upper trapezius as the patient lies supine until the initial resistance barrier is reached. After 7-10 seconds of an isometric shoulder shrug against 20-30% therapist resistance, the participant will relax. Following relaxation, the therapist will gently stretch the new barrier and hold it there for ten to fifteen seconds. This process will be carried out five times. The cervical spine will be positioned in flexion, contralateral side bending, and contralateral rotation for the levator scapulae. The participant will attempt to raise the shoulder against therapist resistance for 7-10 seconds as part of a mild isometric contraction. After that, they will rest and stretch for 10-15 seconds. There will be five repeat

    Other: Muscle Energy Technique + Scapulothoracic Mobilization.

  • Active comparator
    Muscle Energy Technique.

    will be given the identical MET program as Group A for the levator scapulae and upper trapezius muscles. Nevertheless, there won't be any scapulothoracic mobilization. In order to compare results and ascertain the extra impact of scapulothoracic mobilization, this group will solely receive the MET intervention. Participants in both groups will be advised to do a standardized at-home exercise regimen that includes deep cervical flexor activation activities, pectoralis muscle stretching, chin tuck movements, and scapular retraction exercises in addition to the supervised treatment sessions. Stretching exercises will be held for 30 seconds and repeated three times a day, while each exercise will be done in three sets of ten repetitions.

    Other: Muscle Energy Technique.

Interventions

  • OtherMuscle Energy Technique + Scapulothoracic Mobilization.

    will undergo scapulothoracic mobilization after receiving Muscle Energy Technique (MET) that targets the levator scapulae and upper trapezius muscles. The therapist will position the cervical spine in flexion, contralateral side bending, and minor ipsilateral rotation for the upper trapezius as the patient lies supine until the initial resistance barrier is reached. After 7-10 seconds of an isometric shoulder shrug against 20-30% therapist resistance, the participant will relax. Following relaxation, the therapist will gently stretch the new barrier and hold it there for ten to fifteen seconds. This process will be carried out five times. The cervical spine will be positioned in flexion, contralateral side bending, and contralateral rotation for the levator scapulae. The participant will attempt to raise the shoulder against therapist resistance for 7-10 seconds as part of a mild isometric contraction. After that, they will rest and stretch for 10-15 seconds. There will be five repeats

  • OtherMuscle Energy Technique.

    will be given the identical MET program as Group A for the levator scapulae and upper trapezius muscles. Nevertheless, there won't be any scapulothoracic mobilization. In order to compare results and ascertain the extra impact of scapulothoracic mobilization, this group will solely receive the MET intervention. Participants in both groups will be advised to do a standardized at-home exercise regimen that includes deep cervical flexor activation activities, pectoralis muscle stretching, chin tuck movements, and scapular retraction exercises in addition to the supervised treatment sessions. Stretching exercises will be held for 30 seconds and repeated three times a day, while each exercise will be done in three sets of ten repetitions

06

What researchers measure

Primary outcomes

  1. NUMERIC PAIN RATING SCALE

    Numeric Rating Scale (NPRS) is most frequently used instruments to measure pain intensity in low back pain (LBP). The 11-point numeric with 0 representing No pain, 1-3 representing Mild Pain (nagging, annoying, interfering little with ADLs), 4-6 representing Moderate Pains (interferes significantly with ADLs), 7-10 representing Sever Pain (disabling, unable to perform ADLs).

    Time frame: baseline and after 4 weeks

  2. The Neck Disability Index (NDI)

    The Neck Disability Index (NDI) is a ten-item questionnaire based on the Oswestry Low Back Pain Index that assesses disability associated with neck pain and whiplash. It is the most widely used and most strongly validated instrument for assessing self-rated disability in patients with neck pain. It has been used effectively in both clinical and research settings in the treatment of this very common problem. (16) There are four items that relate to subjective symptomatology (pain intensity, headache, concentration, sleeping) and six items that relate to activities of daily living (lifting, work, driving, recreation, personal care, reading). The questionnaire requires only 5-10 minutes to complete and score, and requires no special training to administer. A score of less than 4 indicates no disability, 5-14 mild disability, 15-24 moderate disability, 25-34 severe disability, and scores greater than 35 complete disabilities

    Time frame: baseline and after 4 weeks

  3. CLINOMETER PLUS BUBBLE LEVEL

    The Clinometer application (Plaincode App Development, Google Play Store) on a smartphone will be used to measure active cervical range of motion (ROM) in all six directions: flexion, extension, right and left lateral flexion, and right and left rotation. The participant will be seated upright for flexion, extension, and lateral flexion, and supine for rotation, as the supine position shifts the device into a vertical plane using the accelerometer rather than the magnetometer, resolving the poor rotation validity seen in seated protocols. With SEM ranging from 1.17° to 2.01° and minimal detectable change from 1.18° to 2.02°, the Clinometer application showed moderate to excellent concurrent validity (ICC = 0.544-0.888, p \< 0.01) and moderate to excellent intra rater reliability (ICC = 0.774-0.928) across all six cervical movements, confirming its validity and reliability for measuring active cervical range of motion (40). With the smartphone flat against the corresponding plane of the

    Time frame: baseline and after 4 weeks

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes — The results data collected, de-identified individual participant data will be shared.

Supporting information: Study protocol, Statistical analysis plan, Informed consent form

Time frame: 6 months after the publication of the manuscript.

Access criteria: The data can be requested from the corresponding author.

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Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Nov 3, 2026
Show all 1 update
  1. Nov 3, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07912112
Lead sponsor
University of Management and Technology Lahore
Responsible party
Sponsor
First posted
Nov 3, 2026
Start date
Oct 28, 2026 (estimated)
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Nov 3, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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