ClinicalTrials.gg
Not yet recruitingNCT07791680Updated Aug 28, 2026

Bruegger's Relief Exercise in Chronic Mechanical Neck Pain

An interventional study of Bruegger's Relief Exercise + Conventional Physical Therapy and Conventional Treatment in Chronic Mechanical Neck Pain, sponsored by Riphah International University. Not yet recruiting at 1 site in Pakistan. Open to participants aged 20 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-08-28.

Sponsored by Riphah International University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
44
Allocation
Randomized
Ages
20 Years to 50 Years
Sex
All
01

Where this study stands

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

Among 123 studies in Neck Pain by Riphah International University — 31 open to participants now, 31 under way, none of them phase 3. Neck Pain · Riphah International University.

Planned enrollment
39th of 117
44 · median 40
Started
2026
with 13 others
No phase
117 of 123
31 open now
Primary completion
2027-08
later than 30 of 30 live
Registered
120th of 123
by date

Among the 123 studies in Neck Pain by Riphah International University, this one is the 39th largest by planned enrollment of the 117 interventional ones, is one of 14 that started in 2026, is one of 117 with no phase, reaches primary completion later than 30 of the 30 other live ones, and was the 120th registered.

By phase

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

No phasethis study117 · 31 open
Observational6 · 0 open

By the year they started

First in 2018; this study’s year is marked. 14 started in 2026.

Size and results

Median enrollment 40 across the 117 interventional studies, 114 across the 6 observational. Of the 86 that completed or were terminated, 0 (0%) have results posted.

Was this useful?
Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 123 studies in Neck Pain by Riphah International University, or all of them as a file.
02

Study summary

The aim of this randomized controlled trial is to determine the effect of Bruegger's Relief Exercise combined with conventional physical therapy on pain intensity, functional disability, cervical range of motion, and craniovertebral angle in patients with chronic mechanical neck pain

Read the detailed description

Neck pain is the second most prevalent musculoskeletal disorder worldwide. Neck pain persisting for more than three months is classified as chronic neck pain (CNP). Individuals with chronic mechanical neck pain (CMNP) exhibit distinct neuromuscular and epidemiological characteristics This imbalance contributes to impaired cervical stability and altered movement control.According to the Global Burden of Disease 2019 report, the global age-standardized prevalence of neck pain was approximately 2,696.5 per 100,000 population (≈2.7%), with an incidence rate of 579.1 per 100,000 population (≈0.58%). In Pakistan, musculoskeletal pain among young adults has been reported to range between 55-60%, with neck pain representing a major complaint Forward head posture (FHP) is a common postural deviation associated with chronic mechanical neck pain. It is highly prevalent, affecting approximately 62% of young adults in Pakistan and nearly 64% globally. FHP is characterized by anterior translation of the head, lower cervical flexion, and often increased upper cervical extension. The craniovertebral angle (CVA), defined as the angle formed between a horizontal line through the C7 spinous process and a line connecting the tragus of the ear to C7, is commonly used to quantify forward head posture. A reduced CVA indicates greater forward head translation and has been associated with increased pain intensity and reduced endurance of the deep cervical flexor muscles. Postural deviation and neuromuscular imbalance contribute to mechanical stress on cervical structures, functional limitations, and persistent symptoms in individuals with CMNP.

Given the high prevalence of forward head posture and its association with chronic mechanical neck pain, interventions targeting postural correction and neuromuscular re-education may be clinically beneficial.

This randomized controlled trial aims to evaluate the effect of Bruegger's Relief Exercise combined with conventional physical therapy on pain intensity, functional disability, cervical range of motion, and craniovertebral angle in individuals with chronic mechanical neck pain.

03

Conditions studied

  • Chronic Mechanical Neck Pain

Browse trials for

Keywords

  • Bruegger's Relief Exercise
  • Chronic Mechanical Neck Pain
  • Forward Head Posture
  • Craniovertebral Angle
  • Neck Disability
04

Who can participate

Ages eligible
20 Years to 50 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

    • Participants falling in this category would be recruited into the study.

      • Age 20-50 years
      • Diagnosis of chronic mechanical neck pain (>3 months)
      • Pain intensity ≥ 3/10 on NPRS
      • Neck Disability Index score ≥ 10/50
      • Willing to participate and provide

Exclusion criteria

Exclusion Criteria:

    • Participants falling in this category would be excluded from the study.

      • History of cervical spine fracture or surgery
      • Systemic musculoskeletal or neurological disease
      • Recent whiplash injury (within 6 months)
      • Botulinum toxin injection within previous 6 months
      • Severe structural deformity (e.g., torticollis, severe scoliosis)
      • Red flag signs (fever, unexplained weight loss, progressive neurological deficit)
      • Positive cervical instability tests (Sharp-Purser or Alar ligament test)
      • Clinical signs of cervical radiculopathy (positive Spurling's/ULTT/distraction test)
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
44 participants (estimated)

Study arms

  • Experimental
    Experimental: Bruegger's Relief Exercise + Conventional Physical Therapy

    Bruegger's Relief Exercise + Conventional Physical Therapy

    Other: Bruegger's Relief Exercise + Conventional Physical Therapy

  • Experimental
    Conventional Physical Therapy

    Conventional Physical Therapy

    Other: Conventional Treatment

Interventions

  • OtherBruegger's Relief Exercise + Conventional Physical Therapy

    Bruegger's Relief Exercise. High sitting neutral posture with feet flat on the floor and a light resistance band held across the thighs. 1A gentle chin tuck is performed to maintain cervical alignment. The movement includes 2 shoulder abduction and external rotation 3. Elbow extension 4. Forearm supination 5. Wrist extension 6. Finger and thumb abduction, coordinated with diaphragmatic breathing. (Hold duration: 10-30 seconds with progression of 2 seconds per session). 12 repetitions per session with 30-second rest interval between holds. Total duration is 3 sessions per week for 4 consecutive weeks.

  • OtherConventional Treatment

    Conventional PT including 1- Cervical ROM exercises (flexion, extension, rotation, lateral flexion) 2- Stretching of upper trapezius and levator scapulae (30 sec hold × 3 repetitions) 3- Cervical isometric strengthening in all directions 4- Scapular stabilization exercises (elevation-depression, protraction-retraction) (Dosage: 2-3 sets of 10-15 repetitions). Total duration is 3 sessions per week for 4 consecutive weeks.

06

What researchers measure

Primary outcomes

  1. Numeric Pain Rating Scale

    An 11-point scale (0-10) used to assess pain intensity. 0 indicates no pain and 10 indicates worst imaginable pain. Participants verbally report their pain score

    Time frame: Baseline, Week 2, Week 4

  2. Neck Disability Index

    The NDI is a 10-item questionnaire assessing functional disability related to neck pain. Each item is scored 0-5 with total score range 0-50. Higher scores indicate greater disability.

    Time frame: Baseline, Week 2, Week 4

  3. Cervical Range of Motion

    A universal goniometer will be used to measure cervical flexion, extension, lateral flexion, and rotation

    Time frame: Baseline, Week 2, Week 4

  4. Craniovertebral Angle

    CVA will be measured using the Angle - Video Goniometer mobile application via lateral photographic analysis. A smaller angle indicates greater forward head posture.

    Time frame: Baseline, Week 2, Week

07

Study locations

1 site
  • AR Medical Complex, Mirpur, Azad Kashmir
    Mīrpur, Azad Kashmir 46000, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking 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

Start is estimated for Sep 2026; primary completion for Aug 2027, 11 months later.

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 11 months is above 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
Aug 25, 2026
First posted
Aug 28, 2026
StartEst.
Sep 2026
Primary completionEst.
Aug 1, 2027
CompletionEst.
Aug 5, 2027
Last update
Aug 28, 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.
No changes since tracking began. The registry record was last updated on Aug 28, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07791680
Responsible party
Sponsor
First posted
Aug 28, 2026
Start date
Sep 2026 (estimated)
Primary completion
Aug 1, 2027 (estimated)
Completion
Aug 5, 2027 (estimated)
Last update
Aug 28, 2026

Study contacts

KINZA ANWAR, MS-OMPT
Contact
kinza.anwar@riphah.edu.pk
03319735427
KINZA ANWAR, MS-OMPT
Contact
kinza.anwar@riphah.edu.pk
KINZA ANWAR, MS-OMPT
principal investigator · Riphah International University

Oversight

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

Not currently enrolling

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

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion