NCT07395011

Brief Summary

Many people experience long-lasting neck pain, which can affect daily life, work, and overall well-being. This study aims to find out which type of exercise program is most effective in reducing neck pain, improving neck movement, and making daily activities easier. What Is Being Studied?: The study compares three different types of treatment: DNS Exercises (Dynamic Neuromuscular Stabilization): Whole-body exercises focusing on posture, breathing, and core stability. Localized Neck Exercises: Targeted exercises for the neck and shoulder muscles. Standard Care: Usual physiotherapy treatment commonly provided in clinical practice. Study Procedures: Participants are randomly assigned to one of the three groups. Each participant receives individual exercise instruction from a physiotherapist. Participants are also given simple home exercises to perform on their own. The study lasts for about 12 weeks. What Will Be Measured?: At the beginning, during, and at the end of the study, the following will be assessed: Neck pain intensity (pain scale) Neck range of motion How much the pain affects daily life and activities Possible Benefits: Participants may experience: Less neck pain Improved neck mobility Better overall body awareness Even if not every participant notices improvement, taking part will help researchers improve future treatment options for chronic neck pain. Risks: No major risks are expected. All exercises are supervised by qualified physiotherapists and adjusted to each participant's abilities. Participation can be stopped at any time if discomfort or pain occurs. Voluntary Participation and Data Privacy: Participation is completely voluntary. All personal data will be kept confidential and analyzed anonymously for research purposes only. Participants may withdraw from the study at any time without any disadvantages.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
5mo left

Started Feb 2026

Status
not yet recruiting

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 Progress56%
Feb 2026Dec 2026

First Submitted

Initial submission to the registry

January 31, 2026

Completed
2 days until next milestone

Study Start

First participant enrolled

February 2, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 9, 2026

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

February 9, 2026

Status Verified

January 1, 2026

Enrollment Period

11 months

First QC Date

January 31, 2026

Last Update Submit

January 31, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Numeric Ratic Scale

    From enrollment to the end of treatment at 12 weeks

Secondary Outcomes (3)

  • Neck Disability Index

    From enrollment to the end of treatment at 12 weeks

  • Flexio Rotation Test

    From enrollment to the end of treatment at 12 weeks

  • Fear-Avoidance Beliefs Questionnaire

    From enrollment to the end of treatment at 12 weeks

Study Arms (3)

DNS_Group

EXPERIMENTAL
Other: Dynamic Neuromuscular Stabilization (DNS) Exercises

Local_Exercise

EXPERIMENTAL
Other: Local Exercises

Usual_Care

EXPERIMENTAL
Other: Usual Care

Interventions

Localized neck exercises target deep and superficial cervical muscles through specific strengthening, motor control, and stabilization drills. The program includes chin tucks, resisted movements, and scapular stabilization, supervised by a physiotherapist to improve pain, function, and coordination.

Local_Exercise

Usual care includes standard physiotherapy for chronic neck pain: patient education, manual therapy, heat application, and general stretching or mobility exercises. Treatment follows typical clinical practice and is adjusted to individual needs.

Usual_Care

Dynamic Neuromuscular Stabilization (DNS) is a physiotherapy approach based on developmental kinesiology. It uses specific postural and breathing exercises to restore spinal stability, improve motor control, and enhance cervical function under physiotherapist supervision.

DNS_Group

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • between 18 and 50 years of age. This ensures a homogeneous population that in-cludes both young adults and middle-aged individuals.
  • have suffered from neck pain continuously for at least 12 weeks, as described by the International Association for the Study of Pain (IASP)
  • have current neck pain greater than 40 on the Numeric Rating Scale (NRS) (on a scale of 0 to 100).
  • have an NDI score of over 10 points.

You may not qualify if:

  • Cancer
  • Patients with existing or previous fractures in the cervical spine
  • Patients who have undergone surgery on the cervical spine
  • Patients who, in addition to neck pain, also have or have had dizziness or balance disorders
  • People with osteoporosis
  • Fibromyalgia
  • People with diagnosed rheumatoid arthritis
  • People with red flags identified during a thorough physical examination
  • Patients with neurological deficits identified during a thorough physical examination
  • Participants who have undergone physiotherapy within the last 3 months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Neck Pain

Interventions

Exercise

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 31, 2026

First Posted

February 9, 2026

Study Start

February 2, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

February 9, 2026

Record last verified: 2026-01