- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04809337
Therapeutic Exercises and Stabilization Exercises Given After Manual Therapy
March 19, 2021 updated by: Emine Atıcı, Okan University
Comparison of the Effects of Therapeutic Exercises and Stabilization Exercises After Manual Therapy in Patients With Non-Specific Chronic Neck Pain
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
30
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
-
-
-
İstanbul, Turkey, 34959
- Emine
-
-
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
18 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
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.
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
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Stabilization Exercise Group
|
After manuel therapy, the patients were allocated into two groups as Stabilization Exercise Group and Therapeutic Exercise Group randomly.
|
EXPERIMENTAL: Therapeutic Exercise Group
|
After manuel therapy, the patients were allocated into two groups as Stabilization Exercise Group and Therapeutic Exercise Group randomly.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Visual Analogue Scale
Time Frame: 1 minute
|
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
|
1 minute
|
Range of motion
Time Frame: 10 minute
|
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
|
10 minute
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Lateral Scapular Shift Test
Time Frame: 5 minute
|
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
|
5 minute
|
Neck Disability Index
Time Frame: 3 minutes
|
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
|
3 minutes
|
Bournemouth Neck Pain Questionnaire
Time Frame: 5 minutes
|
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.
|
5 minutes
|
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)
February 1, 2020
Primary Completion (ACTUAL)
September 30, 2020
Study Completion (ACTUAL)
December 1, 2020
Study Registration Dates
First Submitted
March 18, 2021
First Submitted That Met QC Criteria
March 18, 2021
First Posted (ACTUAL)
March 22, 2021
Study Record Updates
Last Update Posted (ACTUAL)
March 23, 2021
Last Update Submitted That Met QC Criteria
March 19, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 005
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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