Therapeutic Exercises and Stabilization Exercises Given After Manual Therapy
Primary Purpose
Patients With Non-Specific Chronic Neck Pain
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Exercise
Sponsored by
About this trial
This is an interventional treatment trial for Patients With Non-Specific Chronic Neck Pain
Eligibility Criteria
Inclusion Criteria:
- Between the ages of 18-65,
- having neck pain for 3 months or longer,
- was diagnosed with chronic neck pain by a specialist.
Exclusion Criteria:
- People with neurological diseases,
- who had previous surgery in the cervical region,
- who had medulla spinalis tumors,
- vascular pathologies,
- fractures,
- osteoporosis,
- rheumatoid arthritis problems were not included in the study.
Sites / Locations
- Emine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Stabilization Exercise Group
Therapeutic Exercise Group
Arm Description
Outcomes
Primary Outcome Measures
Visual Analogue Scale
The Visual Analog Scale (VAS) was developed to transform values which cannot be measured numerically to a numerical form. The patient is instructed to mark the severity of pain on a line marked at one end as 0=no pain to 10=intolerable pain, thereby providing the level of pain in a numerical form
Range of motion
Devices to measure range of motion in the joints of the body include the Goniometer and Inclinometer which use a stationary arm, protractor, fulcrum, and movement arm to measure angle from axis of the joint. We measured neck flexio, extantion and rotation
Secondary Outcome Measures
Lateral Scapular Shift Test
This test involves measuring the distance from the inferior angle of the scapula to the nearest vertebral spinous process using a tape measure or goniometer in three positions: shoulder in neutral, shoulder at 40-45 degrees of coronal plane abduction with hands resting on hips, and the shoulder at 90 degrees abduction with the arms in full internal rotation
Neck Disability Index
The Neck Disability Index (NDI) is a self-report questionnaire used to determine how neck pain affects a patient's daily life and to assess the self-rated disability of patients with neck pain
Bournemouth Neck Pain Questionnaire
Neck Bournemouth Questionnaire (NBQ) was created by Bolton and Humphreys due to the necessity of an evaluation measure to various health domains, such as pain, function, incapacity and psychological and social aspects of patients with neck pathologies. This tool is easily applied, reproducible and responsive to clinical alterations, which makes it adequate to be used for scientific research and clinical practice to monitor the pathology progression and to assist treatment planning.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04809337
Brief Title
Therapeutic Exercises and Stabilization Exercises Given After Manual Therapy
Official Title
Comparison of the Effects of Therapeutic Exercises and Stabilization Exercises After Manual Therapy in Patients With Non-Specific Chronic Neck Pain
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
February 1, 2020 (Actual)
Primary Completion Date
September 30, 2020 (Actual)
Study Completion Date
December 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Okan University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The study was conducted to determine and compare the effects of the therapeutic exercises and stabilization exercises given to the patient after the manual therapy session on pain, neck range of motion, daily living activities and quality of life.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Patients With Non-Specific Chronic Neck Pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Stabilization Exercise Group
Arm Type
Experimental
Arm Title
Therapeutic Exercise Group
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Exercise
Intervention Description
After manuel therapy, the patients were allocated into two groups as Stabilization Exercise Group and Therapeutic Exercise Group randomly.
Primary Outcome Measure Information:
Title
Visual Analogue Scale
Description
The Visual Analog Scale (VAS) was developed to transform values which cannot be measured numerically to a numerical form. The patient is instructed to mark the severity of pain on a line marked at one end as 0=no pain to 10=intolerable pain, thereby providing the level of pain in a numerical form
Time Frame
1 minute
Title
Range of motion
Description
Devices to measure range of motion in the joints of the body include the Goniometer and Inclinometer which use a stationary arm, protractor, fulcrum, and movement arm to measure angle from axis of the joint. We measured neck flexio, extantion and rotation
Time Frame
10 minute
Secondary Outcome Measure Information:
Title
Lateral Scapular Shift Test
Description
This test involves measuring the distance from the inferior angle of the scapula to the nearest vertebral spinous process using a tape measure or goniometer in three positions: shoulder in neutral, shoulder at 40-45 degrees of coronal plane abduction with hands resting on hips, and the shoulder at 90 degrees abduction with the arms in full internal rotation
Time Frame
5 minute
Title
Neck Disability Index
Description
The Neck Disability Index (NDI) is a self-report questionnaire used to determine how neck pain affects a patient's daily life and to assess the self-rated disability of patients with neck pain
Time Frame
3 minutes
Title
Bournemouth Neck Pain Questionnaire
Description
Neck Bournemouth Questionnaire (NBQ) was created by Bolton and Humphreys due to the necessity of an evaluation measure to various health domains, such as pain, function, incapacity and psychological and social aspects of patients with neck pathologies. This tool is easily applied, reproducible and responsive to clinical alterations, which makes it adequate to be used for scientific research and clinical practice to monitor the pathology progression and to assist treatment planning.
Time Frame
5 minutes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Between the ages of 18-65,
having neck pain for 3 months or longer,
was diagnosed with chronic neck pain by a specialist.
Exclusion Criteria:
People with neurological diseases,
who had previous surgery in the cervical region,
who had medulla spinalis tumors,
vascular pathologies,
fractures,
osteoporosis,
rheumatoid arthritis problems were not included in the study.
Facility Information:
Facility Name
Emine
City
İstanbul
ZIP/Postal Code
34959
Country
Turkey
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Therapeutic Exercises and Stabilization Exercises Given After Manual Therapy
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