Efficacy of Kinesiology Tape on Neck Disability
Primary Purpose
Pain, Myofascial Pain Syndrome, Trigger Point Pain, Myofascial
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
kinesiotaping and exercise
exercise
Sponsored by
About this trial
This is an interventional treatment trial for Pain
Eligibility Criteria
Inclusion Criteria:
- age between 18 and 65 years
- symptom duration of at least 3 months
Exclusion Criteria:
- a diagnosis of cervical radiculopathy or myelopathy
- a history of acute neck injury or cervical surgery
- diagnosis of psychiatric disorders
- recent trigger-point injection or participation in a physical treatment program witin the last 6 monhts
- any allergies to the tape and
- having already received treatment with kinesio-taping.
Sites / Locations
- Cansın Medin Ceylan
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
kinesiotaping and exercise
exercise
Arm Description
'I'' strip kinesiotape will be applied with the space correction technique for the upper trapezius muscle, for a total of 4 sessions, 2 days a week, and the patients will be included in the 1-month home exercise program.
1-month home exercise program.
Outcomes
Primary Outcome Measures
visual analog scale
activity and rest pain with visual analog scale '0' no pain '10' severe pain
visual analog scale
activity and rest pain with visual analog scale. '0' no pain '10' severe pain
visual analog scale
activity and rest pain with visual analog scale '0' no pain '10' severe pain
Secondary Outcome Measures
Full Information
NCT ID
NCT05030181
First Posted
July 13, 2021
Last Updated
September 21, 2021
Sponsor
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05030181
Brief Title
Efficacy of Kinesiology Tape on Neck Disability
Official Title
Efficacy of Kinesiology Tape Versus Postural Correction Exercises on Neck Disability in Nonspesific Nek Pain: A Randomized Single Blinded Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
April 1, 2021 (Actual)
Primary Completion Date
June 5, 2021 (Actual)
Study Completion Date
August 31, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Sixty participants with nonspecific neck pain were randomly assigned to either the kinesiotaping (n=30) or exercise (n=30) group.
At the beginning, at the 2nd week and at the 1st month, activity and rest pain with visual analog scale, cervical lateral flexion and rotation with goniometer, neck disability scale and trapezius thickness, trigger point volume, trigger point diameter, trigger point area (with ultrasonograpic imaging) will be evaluated.
After the initial evaluation of the patients in the kinesiotaping group, 'I' strip kinesiotape will be applied with the space correction technique for the upper trapezius muscle, for a total of 4 sessions, 2 days a week, and the patients will be included in the 1-month home exercise program. Patients will be evaluated at the start of treatment, Week 2, and Month.
Patients in the control group will only be included in the 1-month home exercise program. Patients will be evaluated at the start of treatment, Week 2, and Month 1.
The participants inclusion criteria were; age between 18 and 65 years, symptom duration of at least 3 months. The exclusion criteria were as follows: (1) a diagnosis of cervical radiculopathy or myelopathy, (2) a history of acute neck injury or cervical surgery (3) diagnosis of psychiatric disorders (4) recent trigger-point injection or participation in a physical treatment program witin the last 6 monhts (5) any allergies to the tape and (6) having already received treatment with kinesio-taping.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Myofascial Pain Syndrome, Trigger Point Pain, Myofascial
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
single blinded randomized controlled trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
kinesiotaping and exercise
Arm Type
Active Comparator
Arm Description
'I'' strip kinesiotape will be applied with the space correction technique for the upper trapezius muscle, for a total of 4 sessions, 2 days a week, and the patients will be included in the 1-month home exercise program.
Arm Title
exercise
Arm Type
Active Comparator
Arm Description
1-month home exercise program.
Intervention Type
Other
Intervention Name(s)
kinesiotaping and exercise
Intervention Description
kinesiotaping group, ''I'' strip kinesiotape will be applied with the space correction technique for the upper trapezius muscle, for a total of 4 sessions, 2 days a week, and the patients will be included in the 1-month home exercise program.
Intervention Type
Other
Intervention Name(s)
exercise
Intervention Description
exercise
Primary Outcome Measure Information:
Title
visual analog scale
Description
activity and rest pain with visual analog scale '0' no pain '10' severe pain
Time Frame
Baseline
Title
visual analog scale
Description
activity and rest pain with visual analog scale. '0' no pain '10' severe pain
Time Frame
2nd week
Title
visual analog scale
Description
activity and rest pain with visual analog scale '0' no pain '10' severe pain
Time Frame
1st month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age between 18 and 65 years
symptom duration of at least 3 months
Exclusion Criteria:
a diagnosis of cervical radiculopathy or myelopathy
a history of acute neck injury or cervical surgery
diagnosis of psychiatric disorders
recent trigger-point injection or participation in a physical treatment program witin the last 6 monhts
any allergies to the tape and
having already received treatment with kinesio-taping.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
cansın m ceylan
Organizational Affiliation
istanbul physical medicine and rehabilitation research and training hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cansın Medin Ceylan
City
Istanbul
State/Province
None Selected
ZIP/Postal Code
34147
Country
Turkey
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Efficacy of Kinesiology Tape on Neck Disability
We'll reach out to this number within 24 hrs