- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06642688
Immediate Effect of Cervical and Sacroiliac Manipulation on the Autonomic Nervous System and Balance (CSMPAANS)
Comparison Of Spinal Manipulation Applied to the Cervical Spine and Sacroiliac Joints With Pedobarographic Analysis and It's Immediate Effect on the Autonomic Nervous System in Healthy Individuals
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Sinop, Turkey
- Sinop University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Willingness to participate voluntarily.
- Signed informed consent form.
- Age between 18 and 35 years.
- No contraindications for chiropractic practices.
Exclusion Criteria:
- History of orthopedic disabilities related to the lower extremity.
- Ankylosing spondylitis, rheumatoid arthritis.
- History of foot sprain/strain within the past six months.
- Presence of pathologies in the lumbar and sacroiliac regions (herniated discs, spondylosis, spondylolisthesis).
- History of cardiovascular and respiratory diseases.
- Psychiatric disorders such as psychosis and depression.
- Radicular root compressions causing progressive neurological deficits.
- Bleeding/coagulation disorders and receiving anticoagulant treatment.
- Acute fractures and orthopedic trauma.
- Spinal cord tumors and meningeal tumors.
- Intraosseous infections and acute inflammation, such as osteomyelitis.
- Cauda equina syndrome.
- Intracanicular hematomas.
- Spinal cord hematomas in the spine.
- Basilar invagination of the upper cervical region.
- Aneurysmal bone cysts, osteoid osteomas, osteolastomas, giant cell bone tumors.
- Post-surgical fixation prostheses.
- Neoplastic diseases in muscles or other tissues.
- Lhermitte's sign.
- Syringomyelia.
- Vertebral dislocations or hypermobile joints.
- Advanced osteoporosis.
- Vertebrobasilar insufficiency.
Criteria for Withdrawal from the Study:
- Pregnancy or suspicion of pregnancy.
- The volunteer's desire to discontinue participation in the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Sacroiliac Joint Manipulation Group
Sacroiliac joint manipulation was performed on this group in the lateral decubitus position.
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The patient was asked to tie his arms while he was in the side lying position.
The patient's upper knee was flexed and positioned such that it was placed in the popliteal fossa of the lower knee, while the lower knee was in full extension.
Pushing maneuver was performed with HVLA from posterior to anterior and from medial to lateral with pelvic rotation.
The contact point of the sacroiliac joint was PSIS.
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Experimental: Cervical Joint Manipulation Group
Cervical joint manipulation was performed on this group in the supine position.
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Cervical SM was applied supine to restrictions found on motion palpation, according to the technique described by Bergmann and Peterson28 The participant's head and neck were simultaneously rotated and laterally flexed over the contact point-specifically, the posterior supramastoid groove or zygomatic arch (C0-C1), the posterior aspect of the transverse process (C1-C2), or the posterior articular pillar of superior vertebrae (C2-C7) -to the end of passive ROM.
Thereafter, a high-velocity, low-amplitude thrust was delivered in the direction of restricted movement.
Participants with more ROM restriction in the lateral plane were given more lateral-to-medial directed thrusts; participants with more restriction in rotation were given thrusts in the direction of restricted axial rotation; and participants with more restriction in extension were given more anteriorly directed thrusts.
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No Intervention: Control Group
This group did not undergo any interventions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Evaluation of Autonomic Nervous System
Time Frame: In the manipulation groups, measurements were repeated immediately after the manipulation, while in the control group, the initial measurements were repeated 30 minutes later.
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The assessment of the autonomic nervous system was conducted using the Polar H10 device, which is a high-accuracy, gold-standard HRV sensor that comes with a chest-worn strap. The device can connect to multiple components via Bluetooth and ANT+. This device facilitates the measurement of heart rate variability (HRV), R-R intervals, RMSSD (an instantaneous assessment of the parasympathetic system), LF Power (activation of the sympathetic nervous system), HF Power (activation of the parasympathetic nervous system), HF band, and LF/HF ratio (sympathetic-vagal balance). For data analysis, the Elite HRV software supported by the device is utilized. Measurements are conducted while the participant is seated and last approximately one minute. To ensure accurate measurements, it is necessary to moisten the electrode surface before each measurement. During the assessment, the participant should not speak or move |
In the manipulation groups, measurements were repeated immediately after the manipulation, while in the control group, the initial measurements were repeated 30 minutes later.
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Evaluation of Blood Pressure
Time Frame: In the manipulation groups, measurements were repeated immediately after the manipulation, while in the control group, the initial measurements were repeated 30 minutes later.
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Blood pressure of the participants were evaluated with a manual sphygmomanometer on the left arm.
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In the manipulation groups, measurements were repeated immediately after the manipulation, while in the control group, the initial measurements were repeated 30 minutes later.
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Analysis of Pedobarographic Data
Time Frame: In the manipulation groups, measurements were repeated immediately after the manipulation, while in the control group, the initial measurements were repeated 30 minutes later.
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The analysis of pedobarographic data was conducted using METISENS pedobarographic assessment devices.
During the measurements of pressure analysis in individuals participating in our study, static conditions were maintained, and the load distribution on both the right and left feet, as well as the loads on the anterior and posterior aspects of the foot (%), were reported.
Pressure analyses were determined using the Metisens Baropodometric Analysis software, which is the proprietary software that operates in conjunction with the Metisens Pedobarographic Assessment Device (It is not possible to separate these measurements as the device takes all measurements and provides a total analysis.)
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In the manipulation groups, measurements were repeated immediately after the manipulation, while in the control group, the initial measurements were repeated 30 minutes later.
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Evaluation of Pulse
Time Frame: In the manipulation groups, measurements were repeated immediately after the manipulation, while in the control group, the initial measurements were repeated 30 minutes later.
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The pulse of the participants were evaluated with a manual sphygmomanometer on the left arm.
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In the manipulation groups, measurements were repeated immediately after the manipulation, while in the control group, the initial measurements were repeated 30 minutes later.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: SEFA H HATIK, Asst. Prof., Sinop University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CMT0006
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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