- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07395011
The Effectiveness of Dynamic Neuromuscular Stabilization (DNS) Exercises Compared to Localized Exercises and Standard Care on Pain Intensity, Neck Dysfunction, and Upper Cervical Range of Motion in Patients With Chronic Neck Pain: A Pilot Randomized Controlled Trial (RCT) (DYNEX)
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.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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.
Exclusion Criteria: -
- 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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: DNS_Group
|
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.
|
|
Experimental: Local_Exercise
|
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.
|
|
Experimental: Usual_Care
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Numeric Ratic Scale
Time Frame: From enrollment to the end of treatment at 12 weeks
|
From enrollment to the end of treatment at 12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Neck Disability Index
Time Frame: From enrollment to the end of treatment at 12 weeks
|
From enrollment to the end of treatment at 12 weeks
|
|
Flexio Rotation Test
Time Frame: From enrollment to the end of treatment at 12 weeks
|
From enrollment to the end of treatment at 12 weeks
|
|
Fear-Avoidance Beliefs Questionnaire
Time Frame: From enrollment to the end of treatment at 12 weeks
|
From enrollment to the end of treatment at 12 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- WiSo_BA_PTB_WiSe25-26_1_1
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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