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Neck SyndrometheNCT07756125

Suboccipital Release vs Smartphone App Guided Exercises in Smartphone Neck Syndrome

A study testing Suboccipital Release and Smartphone App Guided Exercises in people with Neck Syndrome, run by Riphah International University at 1 site in Pakistan.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Randomized controlled trial comparing suboccipital release and smartphone app-guided exercises on pain, disability, craniovertebral angle and cervical ROM in 52 participants with smartphone neck syndrome over 4 weeks. Read more about this study

Who is it for?
Ages 18 to 30 years
Conditions the study is for
Neck Syndrome
What is being tested?
Suboccipital Release and Smartphone App Guided Exercises
Could I receive a placebo?
No, everyone receives an active treatment
How many people
52 participants
Where
1 sitePakistan
Study dates
13 Aug 2026to 5 Aug 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

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 30 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Adults aged 18 -30 years
  • Both genders
  • Neck pain (>3 months duration)
  • Smartphone use ≥3 h/day
  • Presence of ≥ 3 symptoms (neck pain, upper back pain, shoulder pain, headache, insomnia,intermittent tingling/numbness in upper limbs)
  • Smartphone use with neck flexion ≥ 15°.
Show all 10Show fewer
  • Pain intensity ≥ 3/10 on NPRS
  • Disability score ≥ 10/50 on Neck Disability Index (NDI)
  • Forward head posture with a craniovertebral angle (CVA) < 50
  • Able to understand and independently follow smartphone application-guided

Who cannot join

  • History of cervical spine trauma, surgery, or fracture.
  • Presence of clinically confirmed cervical radiculopathy or objective neurological deficits (e.g., dermatomal sensory loss, myotomal weakness, diminished deep tendon reflexes, or positive clinical tests for cervical radiculopathy).
  • Structural spinal deformities (e.g., scoliosis, torticollis)
  • Presence of acute infection, inflammatory, or systemic musculoskeletal conditions (e.g., rheumatoid arthritis)
  • Vestibular deficits
  • Current participation in other neck pain treatments

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

KINZA ANWAR, MS-OMPT contact

+92-3239735427

kinza.anwar@riphah.edu.pk

Pakistan1 site, 1 recruiting
  • Tariq Medical Centre

    Kallar Kahār, Punjab Province, 46000

    KINZA ANWAR, MS-OMPT, kinza.anwar29@gmail.com

    SANA NAZ, MS-OMPT*

    Recruiting

Other trials in Pakistan

About this study

Official title: Comparison of Suboccipital Release and Smartphone App Guided Exercises in Smartphone Neck Syndrome

Randomized controlled trial comparing suboccipital release and smartphone app-guided exercises on pain, disability, craniovertebral angle and cervical ROM in 52 participants with smartphone neck syndrome over 4 weeks.

Read the detailed description

Smartphone neck syndrome, commonly referred to as text neck syndrome, is a musculoskeletal condition characterized by neck pain, stiffness, and postural dysfunction resulting from prolonged smartphone use. Sustained neck flexion during smartphone viewing increases mechanical stress on the cervical spine, particularly affecting the upper cervical segments and suboccipital musculature. Repetitive forward head posture (FHP) leads to adaptive shortening of posterior cervical muscles, overstretching of anterior cervical structures, altered joint biomechanics, and progressive muscular imbalance.

.Biomechanically, forward head posture increases the load on the cervical spine. As the head moves anteriorly, the gravitational moment arm increases, leading to greater compressive forces on the cervical vertebrae and increased tension in the suboccipital muscles. Continuous activation of these muscles to counterbalance the forward weight of the head results in muscle fatigue, trigger point formation, reduced cervical range of motion (ROM), and pain sensitization. Over time, these alterations may contribute to joint stiffness, decreased mobility, and functional disability.

The craniovertebral angle (CVA) is widely used as an objective measure of forward head posture. A reduced CVA (less than 50 degrees) indicates increased anterior head translation and postural deviation. Decreased CVA has been associated with higher levels of neck pain, muscle tightness, and functional impairment. Additionally, individuals with smartphone neck syndrome commonly demonstrate limited cervical ROM in flexion, extension, rotation, and lateral flexion, along with increased pain intensity and disability scores.

Suboccipital muscle dysfunction plays a central role in smartphone neck syndrome. The suboccipital muscles (rectus capitis posterior major and minor, obliquus capitis superior and inferior) are responsible for fine motor control and stabilization of the atlanto-occipital and atlanto-axial joints. Prolonged flexion posture increases their resting tension and reduces local circulation, potentially leading to ischemia and heightened nociceptive input. Manual therapy techniques such as suboccipital release aim to reduce muscle hypertonicity, improve local blood flow, modulate pain through mechanoreceptor stimulation, and restore normal cervical biomechanics.

On the other hand, exercise-based interventions focus on correcting muscle imbalance and improving neuromuscular control. Chin tucks, suboccipital stretching, and craniovertebral nodding exercises strengthen deep neck flexors, lengthen tight posterior muscles, enhance cervical alignment, and promote long-term postural correction. These exercises also contribute to improved proprioception, muscular endurance, and motor control, which are essential for maintaining cervical stability during daily activities. Physitrack mobile application will be used for app guided exercises.

Recent advancements in digital health technologies have introduced smartphone application-guided rehabilitation programs. Applications such as Physitrack provide structured exercise protocols, instructional videos, reminders, adherence tracking, and feedback mechanisms that enhance patient compliance and self-management. App-guided exercise programs are cost-effective, accessible, and promote continuity of care beyond clinical settings. Evidence suggests that smartphone-based rehabilitation demonstrates strong reliability and validity in monitoring performance and improving musculoskeletal outcomes.

Despite availability of both passive manual therapy and active exercise-based interventions, limited research directly compares the effectiveness of suboccipital release and smartphone app-guided exercises in individuals with smartphone neck syndrome. Passive techniques may provide immediate pain relief and muscle relaxation, whereas active exercise programs may offer long-term improvements in posture, motor control, and functional ability.

Therefore, this study aims to compare the effects of suboccipital release and smartphone app-guided exercises on craniovertebral angle, cervical range of motion, pain intensity, and functional disability in adults with smartphone neck syndrome. The findings of this study may contribute to evidence-based physiotherapy practice by identifying the more effective intervention approach for managing postural dysfunction and neck pain associated with prolonged smartphone

Conditions
Neck Syndrome
Being tested
Suboccipital Release, Smartphone App Guided Exercises
Keywords
Suboccipital Release, Smartphone App Guided Exercises, Smartphone Neck Syndrome

What participants receive

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

  • Suboccipital ReleaseOther

    Suboccipital release technique applied in supine position with sustained bilateral pressure under occiput at C2 level. Duration 4 minutes per session, 3 sessions per week for 4 weeks

  • Smartphone App Guided ExercisesOther

    Chin tucks (10 sec hold, 10 reps), Suboccipital stretch (30 sec hold, 3 reps), Craniovertebral nodding (10 sec hold, 10 reps). 3 sessions per week for 4 weeks. App features include reminders, instructional videos, adherence tracking and feedback.

Study groups in NCT07756125
Study groupRoleWhat they receive
Suboccipital ReleaseExperimentalSuboccipital Release
Receives: Other: Suboccipital Release
Smartphone App Guided ExercisesExperimentalSmartphone App Guided Exercises
Receives: Other: Smartphone App Guided Exercises

What is being measured

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

  1. Numeric Pain Rating Scale

    The Numeric Pain Rating Scale (NPRS) is a simple self-report tool in which patients rate their pain intensity on a scale from 0 (no pain) to 10 (worst imaginable pain).It is widely used in clinical and research settings due to its strong validity, good test-retest reliability, and strong correlation with other pain assessment tools

    Measured: Baseline, 2nd week, 4th week

  2. Neck Disability Index

    The Neck Disability Index (NDI) is a brief, self-administered questionnaire designed to measure disability related to neck pain. It assesses how neck pain affects daily activities and functional status. The NDI is highly reliable and valid, making it a commonly recommended outcome measure in musculoskeletal practice. Lower scores (0-14) mean little to mild neck pain impact on daily tasks. Higher scores (25-50+) indicate severe to complete activity limits,

    Measured: Baseline, 2nd week, 4th week

Timeline

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

  1. First posted10 Aug 2026
  2. Study start13 Aug 2026
  3. Primary completion1 Aug 2027 (estimated)
  4. Study completion5 Aug 2027 (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
Masking
Single blind
Who is masked
Participant
Enrolment
52 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07756125
Sponsor's protocol ID
SANA NAZ
Acronym
the
Status last verified
Aug 2026
First submitted
5 Aug 2026
Last updated
27 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Suboccipital Release and Smartphone App Guided Exercises in people with Neck Syndrome, 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 10 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: looking for participants now, as of the sponsor's last update on 27 Aug 2026. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact KINZA ANWAR, MS-OMPT (+92-3239735427, kinza.anwar@riphah.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Numeric Pain Rating Scale (time frame: Baseline, 2nd week, 4th week). The study lists 2 primary outcomes in all. 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 27 Aug 2026.

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