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NCT Number: NCT07721389

Comparison Between Dynamic Neuromuscular Stabilization Breathing and Manual Therapy on Forward Head Posture in University Students

Forward Head Posture (FHP) is a common postural dysfunction characterized by the anterior displacement of the head relative to the shoulders, leading to cervical spine misalignment, increased muscle strain, and neck pain. It is highly prevalent in university students (63-66%), largely due to prolonged sedentary behaviors and the use of smartphones, laptops, and tablets in poor ergonomic postures .

This randomized controlled trial aims to evaluate the effectiveness of three intervention strategies for managing FHP in university students:

Dynamic Neuromuscular Stabilization (DNS) Breathing + Conventional Exercises: DNS breathing will emphasize diaphragmatic activation and postural stabilization, combined with stretching, strengthening, and postural education.

Myofascial Release (MFR) + Conventional Exercises: Suboccipital MFR to release fascial tension, combined with the same conventional exercise program.

Conventional Exercises Alone (Control Group): A standard rehabilitation protocol of stretching, strengthening, and postural correction.

All interventions will be delivered three times per week for six weeks, with each session lasting 45 minutes.

Assessments will be conducted at baseline, week 4, and week 6:

Craniovertebral Angle (CVA) and Forward Shoulder Angle (FSA) measured using smartphone photographic analysis.

Wall Test to assess forward head and rounded shoulder posture.

Visual Analog Scale (VAS) to measure subjective pain intensity.

SF-36 Health Survey to evaluate quality of life across eight health domains.

The study will compare the relative effectiveness of DNS breathing and MFR, each combined with conventional therapy, against conventional therapy alone. Findings are expected to contribute to evidence-based postural rehabilitation, particularly for young adults with sedentary lifestyles.

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Key information

Age range

18 year–28 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

İstinye University, Fizyoterapi ve Rehabilitasyon Uygulama ve Araştırma Merkezi -İSÜFİZYOTEM

Istanbul, Zeytinburnu, 34010, Turkey (Türkiye)

Location status: Recruiting

Location contact

Dr. Öğr. Üyesi Nurgül Dürüstkan Elbaşı, phd of physical therapy

CONTACT

[email protected]

0850 283 00 00

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

University student aged 18 to 28 years

Presence of forward head posture confirmed by photogrammetric assessment

Mild to moderate cervical pain (VAS score between 0 and 6)

Voluntary agreement to participate in the study

Exclusion criteria

History of cervical spine surgery

Presence of neurological disorders

Diagnosis of cervical disc herniation

Severe musculoskeletal pain (VAS ≥ 7)

Treatment and study plan

Dynamic neuromuscular stabilisation breathing

Other

Diaphragmatic breathing exercises performed in supine, side-lying, and quadruped positions, 3 sets of 1 minute each.

Myofascial Release

Other

Manual sustained pressure applied to the suboccipital region, upper trapezius, and levator scapulae, 2-3 minutes per site, to reduce myofascial stiffness and improve tissue extensibility

Convetional Exercises

Other

Standardized exercise protocol including head rotation, neck/upper back extension, swimmer exercise, head retraction with resistance band, and upper trapezius/levator scapulae stretches.

Primary outcomes

  1. Craniovertebral Angle (CVA)

    Time frame: 4 weeks, and 8 weeks

    The craniovertebral angle (CVA) will be measured using digital photogrammetry to assess the degree of forward head posture. A marker will be placed on the tragus of the ear and the spinous process of C7, and the angle formed between a horizontal line through C7 and the line connecting C7 to the tragus will be calculated. Smaller angles indicate a greater degree of forward head posture.

Secondary outcomes

  1. Visual Analogue Scale (VAS)

    Time frame: Baseline, 4 weeks, and 8 weeks

    Pain intensity will be assessed using a 10 cm Visual Analogue Scale (VAS), where 0 indicates no pain and 10 indicates worst imaginable pain. Participants will mark their perceived pain level at rest and during activity.

Study contacts

Contact information is provided by the study sponsor or research team.

PT Rami M.osama Ramdoun, Bachelor of physical therapy

CONTACT

[email protected]

+905344100383

Prof.Dr. H. Habibe serap INAL, doctor of physical therapy

CONTACT

[email protected]

+905325573354

Sponsors and collaborators

Lead sponsor

Istinye University

Other

Registry information

Official study title

The Effects of Dynamic Neuromuscular Stabilization Breathing and Manual Therapy on Forward Head Posture in University Students: A Randomized Controlled Trial

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jul 23, 2026
Registry last updated
Jul 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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