Short and Long Time Effects of IASTM and Myofascial Release Techniques in Chronic Neck Pain
NCT ID: NCT05683288
Last Updated: 2024-07-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
48 participants
INTERVENTIONAL
2022-12-28
2023-02-22
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Immidate Effect of Instrument Assited Soft Tissue Mobilization Technique on Chronic Neck Pain
NCT04882397
Instrument-assisted Soft Tissue Mobilization and Kinesiotape Application in Individuals With Chronic Neck Pain.
NCT04765670
Comparison of Two Treatments on Nonspecific Neck Pain
NCT06485921
Investigation of the Effect of Instrument Assisted Soft Tissue Mobilization Technique and Foam Roller Application in Individuals With Chronic Non-Specific Neck Pain.
NCT05503602
The Effect of Instrument-assisted Soft Tissue Mobilization Technique on Neck Pain
NCT04803669
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
IASTM
EYYDM will be applied to the upper trapezius and sternocleideomastoid muscles of the participants for 90 seconds, with a frequency of 60 beats per minute. The instruments will be applied to the soft tissue at 30º-60º angles with multidirectional strokes ("stroking") movements.
IASTM
IASTM will be applied to the upper trapezius and sternocleidomastoid muscles of the participants for 90 seconds, with a frequency of 60 beats per minute.
Myofascial Release
Basic movements will be used in the rectus capitis, sternocleidomastoideus, hyoid region and upper trapezius regions within the scope of myofascial release application. The application will take 3 minutes for each region.
Myofascial Release
Basic movements will be performed for 3 minutes in the rectus capitis, sternocleidomastoideus, hyoid region and upper trapezius regions.
Control
It will include 250W infrared application on the cervical region from 50cm away for 15 minutes and TENS application for 20 minutes at 80Hz frequency with 150ms current transit time, home exercise program.
250W infrared application
For 15 minutes, 250W infrared application will be applied on the cervical region from a distance of 50 cm
TENS
TENS will be applied for 20 minutes at 80Hz frequency, with a current transit time of 150ms.
Home exercise
Cervical strengthening and stretching exercises five days a week will given
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
IASTM
IASTM will be applied to the upper trapezius and sternocleidomastoid muscles of the participants for 90 seconds, with a frequency of 60 beats per minute.
Myofascial Release
Basic movements will be performed for 3 minutes in the rectus capitis, sternocleidomastoideus, hyoid region and upper trapezius regions.
250W infrared application
For 15 minutes, 250W infrared application will be applied on the cervical region from a distance of 50 cm
TENS
TENS will be applied for 20 minutes at 80Hz frequency, with a current transit time of 150ms.
Home exercise
Cervical strengthening and stretching exercises five days a week will given
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* To have given at least 3 values to the pain with the Numerical Pain Scale
* having bilateral muscle spasms in the cervical region
Exclusion Criteria
* those with acute injury or infection,
* those with open wounds,
* osteoporosis,
* fracture,
* hematoma,
* those with acute cardiac, liver and kidney problems,
* those with connective tissue disease,
* rheumatoid arthritis, osteoarthritis,
* cancer,
* those with circulation problems,
* those with peripheral vascular disease,
* epilepsy,
* history of surgery in the cervical region
18 Years
44 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
KTO Karatay University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
KTO Karatay University
Konya, Karatay, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
KaratayUH7
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.