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Active, not recruitingNCT07905339Updated Oct 29, 2026

Cervical Stabilization vs Scapular Clock Exercises for Chronic Non-Specific Neck Pain

An interventional study of Cervical Stabilization Exercises and Scapular Clock Exercises in Chronic Non-Specific Neck Pain, sponsored by University of Management and Technology Lahore. Active, not recruiting at 1 site in Pakistan. Open to participants aged 22 Years to 35 Years. Per ClinicalTrials.gov, last updated 2026-10-29.

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

Updated Oct 29, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
22 Years to 35 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 205 studies in Neck Pain with a site in Pakistan — 52 open to participants now, 60 under way, none of them phase 3. Neck Pain · Pakistan.

Enrollment
153rd of 195
30 · median 42
Started
2026
with 35 others
No phase
195 of 205
52 open now
Primary completion
2026-12
later than 46 of 59 live
Registered
197th of 205
by date
Lead sponsor
7 of 205
University of Management and Technology Lahore

Among the 205 studies in Neck Pain with a site in Pakistan, this one is the 153rd largest by enrollment of the 195 interventional ones, is one of 36 that started in 2026, is one of 195 with no phase, reaches primary completion later than 46 of the 59 other live ones, and was the 197th registered.

By phase

205 studies; the count open now beside each. This study's row is marked.

No phasethis study195 · 52 open
Observational10 · 0 open

By the year they started

First in 2017; this study’s year is marked. 36 started in 2026.

Size and results

Median enrollment 42 across the 195 interventional studies, 128 across the 10 observational. Of the 131 that completed or were terminated, 0 (0%) have results posted.

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Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 205 studies in Neck Pain with a site in Pakistan, or all of them as a file.
02

Study summary

This randomized clinical trial will compare cervical stabilization exercises with scapular clock exercises in 30 adults with chronic non-specific neck pain. Participants will be allocated to Group A (cervical stabilization exercises) or Group B (scapular clock exercises), with 15 participants in each group. Both groups will receive three supervised sessions per week for six weeks (18 sessions; approximately 30-40 minutes per session), along with a 10-minute cervical hot pack, pain-free active cervical range-of-motion exercises, postural education, and home-exercise instructions. Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS), cervical range of motion using a inclinometer, and neck-related disability using the Neck Disability Index (NDI), before treatment and at the end of six weeks. The study aims to compare changes in pain, cervical mobility, and disability between the two exercise approaches

03

Conditions studied

  • Chronic Non-Specific Neck Pain

Browse trials for

Keywords

  • Neck Pain
  • cervical stabilization exercises
  • scapular clock exercises
  • range of motion
04

Who can participate

Ages eligible
22 Years to 35 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

Adults aged 22-35 years. Male and female participants. Chronic non-specific neck pain lasting more than 12 weeks. Ability to understand and follow exercise instructions. Neck Disability Index (NDI) score indicating mild to moderate disability. NPRS score of 3-6

Exclusion criteria

Exclusion Criteria:

History of cervical fracture, tumor, infection, or cervical spine surgery. Cervical radiculopathy or myelopathy. Neurological disorders affecting the neck or upper limbs. Recent trauma to the cervical spine. Rheumatologic or systemic inflammatory diseases.

05

Study design

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

Study arms

  • Experimental
    Cervical Stabilization Exercises

    Participants will perform cranio-cervical flexion, chin-tuck, deep cervical flexor activation, and cervical isometric exercises. Exercises will progress over six weeks, with quadruped cervical stabilization and controlled upper-limb movements introduced during weeks 5-6.

    Other: Cervical Stabilization Exercises

  • Active comparator
    Scapular Clock Exercises

    Group B - Scapular Clock Exercises: Participants will practice scapular elevation (12 o'clock), protraction (3 o'clock), depression (6 o'clock), and retraction (9 o'clock), progressing to wall-based, multidirectional, and diagonal clock patterns. Both groups will receive three sessions weekly for six weeks, each approximately 30-40 minutes, plus the same conventional care and postural education described above.

    Other: Scapular Clock Exercises

Interventions

  • OtherCervical Stabilization Exercises

    Participants will perform cranio-cervical flexion, chin-tuck, deep cervical flexor activation, and cervical isometric exercises. Exercises will progress over six weeks, with quadruped cervical stabilization and controlled upper-limb movements introduced during weeks 5-6

  • OtherScapular Clock Exercises

    Participants will practice scapular elevation (12 o'clock), protraction (3 o'clock), depression (6 o'clock), and retraction (9 o'clock), progressing to wall-based, multidirectional, and diagonal clock patterns. Both groups will receive three sessions weekly for six weeks, each approximately 30-40 minutes, plus the same conventional care and postural education described above

06

What researchers measure

Primary outcomes

  1. . Numeric Pain Rating Scale (NPRS)

    An 11-point scale used to rate pain intensity (3). A score of 0 means no pain. Scores of 1 to 3 are mild pain (nagging, annoying, and interferes little with ADLs). Scores of 4 to 6 are moderate pain (interferes significantly with ADLs). Scores of 7 to 10 are severe pain (disabling, unable to perform ADLs). Patients rate their current shoulder pain at baseline and after six weeks.

    Time frame: baseline and after 6 weeks

  2. Goniometric range of motion

    The smartphone inclinometer is a mobile version of a medical device called an inclinometer that can be used to measure joint range of motion (ROM) accurately and objectively. It uses the smartphone's sensors to determine angle of displacement and outputs the reading in degrees. Smartphones are valid, reliable, cost-effective tools to measure neck ROM in real-world clinical and research settings

    Time frame: baseline and after 6 weeks

  3. NECK DISABILITY INDEX (NDI)

    The Neck Disability Index (NDI) will be used to assess functional disability related to neck pain. It consists of 10 items; each scored from 0 to 5. The total score ranges from 0 to 50,with higher scores indicating greater disability. The NDI is a valid and reliable self-reported questionnaire and is one of the most widely used instruments for measuring neck-related disability in individuals with chronic non-specific neck pain.

    Time frame: baseline and after 6 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

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Oct 2026 (actual). Primary completion is estimated for Dec 2026, 2 months after the start.

Of 763 non-industry interventional studies with no phase under Neck Pain, half reached primary completion within 7 months of starting (the median), counting those still running; a quarter within 3 and three quarters within 15. This study's planned 2 months is below that.

Counting every sponsor, half of 772 studies reached it within 7 months; a quarter within 3 and three quarters within 15.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 22, 2026
First posted
Oct 29, 2026
StartActual
Oct 22, 2026
Primary completionEst.
Dec 31, 2026
CompletionEst.
Dec 31, 2026
Last update
Oct 29, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 29, 2026
Show all 1 update
  1. Oct 29, 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
NCT07905339
Lead sponsor
University of Management and Technology Lahore
Responsible party
Rabia Majeed (Dr. Rabia Majeed, Assistant Professor, University of Management and Technology Lahore) — Principal investigator
First posted
Oct 29, 2026
Start date
Oct 22, 2026
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Oct 29, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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