NCT07601880

Brief Summary

Postural deviations of the cervical spine, particularly forward head posture (FHP) and altered cervical lordosis, are increasingly common in individuals with prolonged use of computers, mobile phones, and poor sitting posture. These deviations lead to muscular imbalances where weak deep cervical stabilizers coexist with tight, overactive muscles such as the upper trapezius and sternocleidomastoid. The biomechanical consequences include excessive stress on cervical joints, impaired proprioception, reduced cervical range of motion, and a predisposition to chronic neck pain, cervicogenic headaches, and even temporomandibular disorders. Myofascial trigger points (MTrPs) in the sternocleidomastoid and upper trapezius are frequently implicated in these conditions, contributing to pain, stiffness, and sensorimotor dysfunction. Trigger points are characterized by taut muscle bands, localized hypoxia, biochemical mediators of pain, and neuromuscular hyperexcitability. Treatments such as dry needling (DN) aim to mechanically disrupt this pain-spasm cycle by reducing motor end plate irritability and sympathetic overactivity, whereas phonophoresis (PH) enhances trans-dermal absorption of anti-inflammatory or analgesic drugs using ultrasound, providing a non-invasive alternative for pain management. Given the high prevalence of cervical postural deviations and the burden of associated pain and disability, there is a need to identify the most effective intervention for MTrPs in this population. This study, therefore, proposes a randomized controlled trial comparing the effects of dry needling and phonophoresis on pain, cervical range of motion, and postural correction in patients with FHP and altered cervical lordosis. The findings aim to guide clinicians in selecting evidence-based treatments to optimize outcomes for patients with cervical spine abnormalities. Study Design: Randomized Control Trial No of groups: 40 (men and women aged 20-55 year) 20 receiving phonophoresis and 20 receiving Dry Needling. Outcomes:

  1. 1.Reduction in Neck Pain
  2. 2.Cervical Range of Motion

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 25, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

May 15, 2026

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 15, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

May 22, 2026

Completed
Last Updated

May 22, 2026

Status Verified

January 1, 2026

Enrollment Period

4 months

First QC Date

May 15, 2026

Last Update Submit

May 15, 2026

Conditions

Keywords

Dry NeedlingPhonophoresisMyofascial Trigger pointsCervical postural DeviationNeck PainCervical Range of Motion

Outcome Measures

Primary Outcomes (2)

  • Regain Range Of motion

    Cervical Range of motion. These ranges are taken by Goniometer.

    4 weeks

  • Reduce Neck Pain.

    Reduction in neck pain and for its measurement we use Numeric pain rating scale.

    4 weeks

Study Arms (2)

Group 1

EXPERIMENTAL

Real Dry needling + sham phonophoresis

Procedure: Group 1

Group 2

EXPERIMENTAL

Sham dry needling + real phonophoresis

Radiation: Group 2

Interventions

Group 2RADIATION

* Diclofenac Sodium medication will be used with ultrasound. * Ultrasound waves with 1.2 w/cm intensity 60 percent duty cycle will be applied by a Pulsed 1 MHz ultrasound unit for 5 minutes on MTPs Baseline Treatment is stretching

Also known as: Phonophoresis, dexamethasone
Group 2
Group 1PROCEDURE

•0.25 × 40 millimeter sterilized needle, We will insert the steralized needle into subcutaneous tissue in a position perpendicular to muscle. The needle tip will be inserted into the muscle until a local twitch response is elicited. The same point will be needled for about 60 seconds by rapid inward and outward needle movements Baseline Treatment is stretching

Also known as: Dry Needling
Group 1

Eligibility Criteria

Age20 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Chronic Neck pain
  • Trigger points in Trapezius and Levetor Scapulae
  • Duration of Pain from at least 3 months

You may not qualify if:

  • Person's History of Neck Surgery
  • Local Hemmorhage
  • Active infections and Open wounds
  • Bleeding disorders
  • use of alcohol or any material that disturbs the consciousness

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ghurki Trust Teaching Hospital

Lahore, Punjab Province, 57000, Pakistan

Location

Related Publications (1)

  • Abbaszadeh-Amirdehi M, Ansari NN, Naghdi S, Olyaei G, Nourbakhsh MR. Therapeutic effects of dry needling in patients with upper trapezius myofascial trigger points. Acupunct Med. 2017 Apr;35(2):85-92. doi: 10.1136/acupmed-2016-011082. Epub 2016 Oct 3.

    PMID: 27697768BACKGROUND

Related Links

MeSH Terms

Conditions

Neck Pain

Interventions

PhonophoresisDexamethasoneDry Needling

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Drug Administration RoutesDrug TherapyTherapeuticsPregnadienetriolsPregnadienesPregnanesSteroidsFused-Ring CompoundsPolycyclic CompoundsSteroids, FluorinatedComplementary TherapiesPhysical Therapy Modalities

Study Officials

  • Umber Nawaz

    UBAS

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
By simply not informing about the group allocation
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant professor

Study Record Dates

First Submitted

May 15, 2026

First Posted

May 22, 2026

Study Start

January 25, 2026

Primary Completion

May 15, 2026

Study Completion

May 15, 2026

Last Updated

May 22, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations