- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06578481
The Effectiveness of Postural Stabilization Exercises in Patients With Chronic Neck Pain
August 27, 2024 updated by: Gölgem Mehmetoğlu, European University of Lefke
The Effect of Postural Stabilization Exercises on Craniovertebral Angle, Disability and Quality of Life in Patients With Chronic Neck Pain: Randomized Controlled Trial
This study aimed to evaluate the effect of postural stabilization exercises given in addition to cervical stabilization on craniovertebral angle, neck disability index, and quality of life in people with chronic neck pain.Sixty women with chronic neck pain between the ages of 20-60 were included in the study and the individuals were randomly divided into two groups.
Individuals in the first group underwent cervical stabilization (CS) exercises and additional scapular and lumbopelvic stabilization (SLPS) exercises three times a week for 6 weeks.
The second group was treated with only CS exercises for the same period.
In addition, stretching exercises and a 20-minute hot pack were applied to the muscles around the neck of all patients.
Craniovertebral angle (CVA) was measured by photogrammetry.
Disability level was measured by the Neck Disability Index (NDI).
The Turkish version of the Short Form-36 (SF-36) was used to assess quality of life.
Study Overview
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Gemikonağı
-
Lefka, Gemikonağı, Cyprus, 99790
- European University of Lefke
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- The study included females between the ages of 20-60 years, with moderate pain intensity (3 cm and above according to the Visual Pain Scale) and neck pain lasting more than 3 months.
Exclusion Criteria:
- Participants who had undergone any shoulder or neck surgery complained of fibromyalgia and myofascial pain syndrome, had a neurological disease, cervical radiculopathy, and serious systemic disease that would interfere with treatment, and who were pregnant were excluded from the study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: SLPS Group
Scapular and lumbopelvic stabilization group
|
Individuals in the first group underwent cervical stabilization (CS) exercises and additional scapular and lumbopelvic stabilization (SLPS) exercises three times a week for 6 weeks.
The second group was treated with only CS exercises for the same period.
In addition, stretching exercises and a 20-minute hot pack were applied to the muscles around the neck of all patients.
|
|
Active Comparator: CS group
Cervical stabilization group
|
Individuals in the first group underwent cervical stabilization (CS) exercises and additional scapular and lumbopelvic stabilization (SLPS) exercises three times a week for 6 weeks.
The second group was treated with only CS exercises for the same period.
In addition, stretching exercises and a 20-minute hot pack were applied to the muscles around the neck of all patients.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Craniovertebral Angle Measurement
Time Frame: 6 weeks
|
The craniovertebral angle (CVA) is formed by the intersection of a horizontal line passing through the seventh cervical vertebra in the sagittal plane and a line going to the tragus of the ear
|
6 weeks
|
|
Neck Disability Index
Time Frame: 6 weeks
|
The Neck Disability Index was used to assess the disability of people with chronic neck pain during daily activities
|
6 weeks
|
|
Health Related Quality of Life
Time Frame: 6 weeks
|
The Turkish version of the Short Form-36 (SF-36) is used to assess health-related quality of life.
Short Form-36 (SF-36) is a self-assessment scale and analyses 8 dimensions of health
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 28, 2022
Primary Completion (Actual)
December 30, 2022
Study Completion (Actual)
December 30, 2022
Study Registration Dates
First Submitted
August 26, 2024
First Submitted That Met QC Criteria
August 27, 2024
First Posted (Actual)
August 29, 2024
Study Record Updates
Last Update Posted (Actual)
August 29, 2024
Last Update Submitted That Met QC Criteria
August 27, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- EULefke
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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