- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04830098
Comparison of the Effectiveness of Spinal Stabilization Exercises and Chiropractic Spinal Manipulation
Comparison of the Effectiveness of Spinal Stabilization Exercises and Chiropractic Spinal Manipulation in Healthy Individuals
It is the study of the effectiveness of spinal stabilization exercises and chiropractic spinal manipulation in healthy individuals.
In addition, it was planned to investigate the effects of spinal stabilization exercises and manipulation on muscle strength, muscular endurance, balance and proprioception, depression and quality of life.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
It is the study of the effectiveness of spinal stabilization exercises and chiropractic spinal manipulation in healthy individuals.
In addition, it was planned to investigate the effects of spinal stabilization exercises and manipulation on muscle strength, muscular endurance, balance and proprioception, depression and quality of life.
Eighty healthy individuals between the ages of 18-45 who voluntarily participated in the study from students or academic/administrative staff at Gümüşhane University were included in the study. The study program was explained to the participants in line with the Informed Consent Form. It was included in the study after the relevant form was signed by the participant.
Healthy individuals to participate in the study will be randomly divided into 4 groups; randomization will be done by "Research Randomizer" computer program. Group 1 Stabilization group (n = 20), Group 2 Manipulation group (n = 20), Group 3 Stabilization and Manipulation group (n = 20), Group 4 Control group (n = 20). Group 1 will be given stabilization exercises for a total of 18 sessions, 3 times a week for 6 weeks, each session for 45 minutes. Group 2 will be applied high-speed low-amplitude (HVLA) chiropractic manipulation for a total of 6 sessions, once a week for 6 weeks. Group 3 will be given both stabilization exercises and manipulation exercises. The fourth group will be followed as a control group and no application will be made. Prone plunk, side plunk and sorenson tests for muscular endurance in the individuals participating in the study; Quadriceps muscle strength for muscle strength assessment; Joint position sense for propioception; Y balance test for balance; Short Form-36 (SF-36) for quality of life; Beck Depression Inventory was planned to be evaluated before, after and 1 months for psychosomatic evaluation.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Gumushane, Turkey, 29000
- Gumushane University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy volunteer individuals (Female and Male),
- Between the ages of 18-45,
- No pain, trauma or surgery history in the last 6 months,
- Without any chronic disease (Obesity, Diabetes, Hypertension, Osteoporosis),
- Individuals who had not received any treatment for spinal problems before were included in the study.
Exclusion Criteria:
- Conditions where chiropractic spinal manipulation is contraindicated (Inflammation, infection, malignancy, blood coagulation disorder, etc.)
- Any injury during the working process,
- Individuals who did not attend the work program regularly were not included in the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Stabilization group
Stabilization group will be given stabilization exercises for a total of 18 sessions, 3 times a week for 6 weeks, each session for 45 minutes.
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It will be given stabilization exercises for a total of 18 sessions, 3 times a week for 6 weeks, each session for 45 minutes.
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Experimental: Manipulation group
Manipulation group be applied high-speed low-amplitude (HVLA) chiropractic manipulation for a total of 6 sessions, once a week for 6 weeks.
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It will be applied high-speed low-amplitude (HVLA) chiropractic manipulation for a total of 6 sessions, once a week for 6 weeks.
|
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Experimental: Stabilization and Manipulation group
Stabilization and Manipulation group will be given both stabilization exercises and manipulation exercises.
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It will be given stabilization exercises for a total of 18 sessions, 3 times a week for 6 weeks, each session for 45 minutes.
It will be applied high-speed low-amplitude (HVLA) chiropractic manipulation for a total of 6 sessions, once a week for 6 weeks.
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No Intervention: Control group
No application will be made in the control group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Joint position sense change
Time Frame: Before starting study, after the study is finished, 1 month after the end of the study
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The knee to be evaluated in a closed and quiet environment was positioned at 60 degrees of flexion joint angle for five seconds, and the person was asked to perceive this angular position.
Then, the knee was relaxed and the person was asked to return to the joint position he perceived and hold for five seconds at that point.
The difference is considered as the error angle.
The error angle was calculated by taking the average of 3 trials.
Measurements were made with the participants' eyes closed
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Before starting study, after the study is finished, 1 month after the end of the study
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Quadriceps muscle strength change
Time Frame: Before starting study, after the study is finished, 1 month after the end of the study
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During the test, after the participant completed the maximum knee extension, the evaluator stabilized the applied thigh with one hand and placed the dynamometer perpendicular to the leg 1-2 cm above the level of the malleoli with the other hand.
A thin towel was placed between the dynamometer and the leg so that the dynamometer did not hurt the leg during the measurement.
During the test, the "make test" technique, which requires isometric contraction, was applied.
(Make test is the protocol of the person applying the maximum force against the device while the meter keeps the dynamometer constant).
After the knee extension was completed, the participant was asked to maintain the maximum isometric contraction for 5 seconds.
The average of 3 consecutive maximum contraction measurement values made at 30-second intervals was calculated
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Before starting study, after the study is finished, 1 month after the end of the study
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Y balance test change
Time Frame: Before starting study, after the study is finished, 1 month after the end of the study
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It was used for dynamic balance of individuals.
The validity reliability of the test was determined by Plisky et al.
ICC range was 0.85-0.01
intrarater and 0.99-1.00
interrater [30].
The amount of lying on the dominant extremities of the individuals was measured.
The subject was asked to stand on one foot at the midpoint of the test setup and touch with the tip of the toe while maintaining his balance with the other foot in the anterior, posteromedial and posterolateral directions.
The test was repeated 3 times in all directions, averaged and recorded in cm.
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Before starting study, after the study is finished, 1 month after the end of the study
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Prone Plank Test change
Time Frame: Before starting study, after the study is finished, 1 month after the end of the study
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It is a valid and reliable test used to measure the endurance of core region muscles [27].
The participant is asked to lie face down and rise on their elbows and toes while keeping the body in a straight line.
The total time is recorded.
The time is stopped if the participant lowers or lifts his body.
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Before starting study, after the study is finished, 1 month after the end of the study
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Side Plank Test change
Time Frame: Before starting study, after the study is finished, 1 month after the end of the study
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It evaluates the endurance of the lateral trunk flexor muscles.
The participant is asked to lie on his side on the elbow with the legs in full extension.
Participant is asked to lift the lower limbs so that the hips and back are aligned and maintain this position.
The total time is recorded.
If the participant dropped his hip, the time was stopped.
Measurements were repeated on both sides, right and left.
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Before starting study, after the study is finished, 1 month after the end of the study
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Sorenson test change
Time Frame: Before starting study, after the study is finished, 1 month after the end of the study
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Participant lies face down with his torso hanging from the table above the Anterior Superior Iliac Spine (ASIS) level.
Thighs and legs are stabilized using straps.
Participant then places his hands diagonally on the shoulders and is asked to lift his body at the same level with the table.
Participant is asked to hold this position as long as possible and the total time is recorded.
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Before starting study, after the study is finished, 1 month after the end of the study
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Short Form-36 change
Time Frame: Before starting study, after the study is finished, 1 month after the end of the study
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Developed to evaluate the quality of life, this scale was developed by Koçyiğit et al.
Turkish validity and reliability study was conducted by [33].
SF-36 is a 36-item scale that includes physical and mental health inquiries.
The high score obtained from the scale, which is evaluated between 0 and 100 points, indicates good health.
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Before starting study, after the study is finished, 1 month after the end of the study
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Beck Depression Inventory change
Time Frame: Before starting study, after the study is finished, 1 month after the end of the study
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Hisli et al.
It is a scale consisting of 21 items, whose Turkish validity and reliability study was conducted by [35].
The high score obtained from the scale, which is between 0 and 63 points, indicates the presence of high depression.
0-9 points are defined as minimal depression, 10-16 points mild depression, 17-29 points moderate depression, and 30-63 points severe depression.
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Before starting study, after the study is finished, 1 month after the end of the study
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Collaborators and Investigators
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
Other Study ID Numbers
- CHRİOEXERCİSE001
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
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