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Neck Pain MusculoskeletalPBUNCT07266610

Effects of Neck Stabilizers Retraining on Chronic Neck Pain

A study testing Biofeedback-assisted deep neck flexor retraining and Conventional exercises in people with Neck Pain Musculoskeletal and Chronic Neck Pain, run by Lahore University of Biological and Applied Sciences at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The present study aims to evaluate the effects of deep neck stabilizers retraining with pressure biofeedback on cervical range of motion, pain, and temporomandibular dysfunction in patients with chronic neck pain. Read more about this study

Who is it for?
Ages 18 to 30 years
Conditions the study is for
Neck Pain Musculoskeletal, Chronic Neck Pain
What is being tested?
Biofeedback-assisted deep neck flexor retraining and Conventional exercises
Could I receive a placebo?
No, everyone receives an active treatment
How many people
70 participants
Where
1 sitePakistan
Study dates
28 Nov 2025to 13 May 2026
Phase
Interventional
Are there results?
None posted in the registry

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

  • Diagnosis: Chronic neck pain (duration more than 3 months and less than 1 year and 6 months)
  • TMJ Dysfunction (RCD TMJ Axis I Confirmation on Helkino Index) Fonseca Anamnestic Index (FAI) 20-65 score mild to moderate

Who cannot join

  • Traumatic neck injury
  • Neurological disorders
  • Cervical spine infection or surgery
  • Cancer

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Pakistan Society for the Rehabilitation of the Disabled (PSRD)

    Lahore, Punjab Province

Other trials in Pakistan

About this study

Official title: Effects of Deep Neck Stabilizers Retraining With Pressure Biofeedback on Cervical Pain, Range of Motion and Temporomandibular Dysfunction in Patients With Chronic Neck Pain

The present study aims to evaluate the effects of deep neck stabilizers retraining with pressure biofeedback on cervical range of motion, pain, and temporomandibular dysfunction in patients with chronic neck pain.

Participants will receive biofeedback-assisted deep neck flexor retraining in one group, while the other group will perform conventional exercises. The neurological connection between the TMJ and neck means that therapies such as neck flexion exercises and biofeedback can alleviate neck pain and jaw issues.

Read the detailed description

Chronic neck pain is increasingly affecting young adults in Pakistan. This rise is linked to poor posture, being overweight, aging, and various other factors. Weakness in deep neck muscles can affect neck stability. The craniocervical flexion test (CCFT) is useful for evaluating and engaging these muscles. The jaw joint (Temporomandibular joint) and the neck are closely connected through shared nerves. Therefore, problems in the neck can lead to jaw issues (pain and difficulty moving the jaw). Using biofeedback to train deep neck muscles helps improve muscle control, posture, and reduces stress on surface and jaw muscles, easing TMJ symptoms. However, many studies on deep neck stabilizer (DNS) exercises don't focus on jaw problems. This study utilizes pressure biofeedback to relieve pain, improve mobility, and reduce jaw tension by promoting better neck posture.

Being tested
Biofeedback-assisted deep neck flexor retraining, Conventional exercises
Keywords
Chronic neck pain, Deep neck stabilizers, Pressure biofeedback, Temporomandibular dysfunction
Medical subject headings
Temporomandibular Joint Disorders

What participants receive

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

  • Biofeedback-assisted deep neck flexor retrainingOther

    The experimental group will receive deep neck stabilizer training with pressure biofeedback and traditional exercises for six weeks, three times weekly.

  • Conventional exercisesOther

    The control group will engage in a traditional exercise program for 6 weeks, meeting three times weekly

Study groups in NCT07266610
Study groupRoleWhat they receive
Group 1 (Biofeedback-assisted deep neck flexor retraining )ExperimentalEach session includes TENS and hot pack therapy, crook lying exercises with a 20 mmHg pressure biofeedback sensor, the Cranio-Cervical Flexion Test, and neck and shoulder stretches. Data will be collected at the initial point, after 3 weeks, and once more at the 6-week point.
Receives: Other: Biofeedback-assisted deep neck flexor retraining
Group 2 (Conventional exercises)Active comparatorEach session begins with TENS and hot pack therapy, followed by stretching and strengthening exercises for neck and shoulder muscles. Data will be collected at the initial point, after 3 weeks, and once more at the 6-week point.
Receives: Other: Conventional exercises

What is being measured

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

  1. Temporomandibular dysfunction

    Mandibular Functional Impairment Questionnaire

    Measured: 6 weeks

  2. Pain Intensity

    Numeric Pain Rating Scale will be used

    Measured: 6 weeks

  3. Cervical Range of Motion

    Inclinometer

    Measured: 6 weeks

Timeline

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

  1. First posted5 Dec 2025
  2. Study start28 Nov 2025
  3. Primary completion13 May 2026
  4. Study completion13 May 2026

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
Model description
2 groups Experimental group (Group 1): deep neck stabilizers training through pressure biofeedback, along with a traditional exercise program Control group (Group 2): traditional exercise program
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
70 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07266610
Sponsor's protocol ID
UBAS/ERB/FoRS/25/024
Other IDs
U1111-1331-6077
Acronym
PBU
Status last verified
Dec 2025
First submitted
24 Nov 2025
Last updated
18 May 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Sikka I, Chawla C, Seth S, Alghadir AH, Khan M. Effects of Deep Cervical Flexor Training on Forward Head Posture, Neck Pain, and Functional Status in Adolescents Using Computer Regularly. Biomed Res Int. 2020 Oct 5;2020:8327565. doi: 10.1155/2020/8327565. eCollection 2020.

    PubMed 33083487
  • Alagingi NK. Chronic neck pain and postural rehabilitation: A literature review. J Bodyw Mov Ther. 2022 Oct;32:201-206. doi: 10.1016/j.jbmt.2022.04.017. Epub 2022 Apr 20.

    PubMed 36180150
  • Aguiar ADS, Nogueira Carrer HC, de Lira MR, Martins Silva GZ, Chaves TC. Patient-Reported Outcome Measurements in Temporomandibular Disorders and Headaches: Summary of Measurement Properties and Applicability. J Clin Med. 2021 Aug 26;10(17):3823. doi: 10.3390/jcm10173823.

    PubMed 34501273
  • Craciun MD, Geman O, Leuciuc FV, Holubiac IS, Gheorghita D, Filip F. Effectiveness of Physiotherapy in the Treatment of Temporomandibular Joint Dysfunction and the Relationship with Cervical Spine. Biomedicines. 2022 Nov 17;10(11):2962. doi: 10.3390/biomedicines10112962.

    PubMed 36428529

Questions about this trial

What is this clinical trial studying?

A study testing Biofeedback-assisted deep neck flexor retraining and Conventional exercises in people with Neck Pain Musculoskeletal and Chronic Neck Pain, run by Lahore University of Biological and Applied Sciences 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 2 inclusion and 4 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: finished, as of the sponsor's last update on 18 May 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Temporomandibular dysfunction (time frame: 6 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07266610, which also lists 4 linked publications.

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 18 May 2026.

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