Lordosis; PosturalWBVNCT06521983
The Effect of Whole Body Vibration on Muscle Elasticity
A study testing Whole body vibration in people with Lordosis; Postural and Lordosis, run by Gaziantep Islam Science and Technology University at 1 site in Turkey (Türkiye).
Trial summary
This study examined the effect of whole-body vibration on pain and muscle elasticity in individuals with hyperlordosis and normal lordosis. Flexible ruler for individuals' spinal curvatures (lumbar lordosis); back-lower back pain levels VAS; muscle elasticity Myoton Pro device; Physical functions will be evaluated… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Lordosis; Postural, Lordosis, Hyperlordosis
- What is being tested?
- Whole body vibration
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 28 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 5 Nov 2023to 28 Jun 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Being over 18 years of age,
- Having pain >5 according to VAS measurement,
- Having normal lumbar lordosis angle between 30°-40°,
- Having hyperlordosis angle >40°
Who cannot join
- Having Scheurmann kyphosis, ,
- Having scoliosis (Cobb angle >10°),
- Having other congenital spine abnormalities
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Gaziantep Islam Science and Technology University
Gaziantep
About this study
Official title: The Effect of Whole Body Vibration on Pain and Muscle Elasticity in Individuals With Hyperlordosis and Normal Lordosis
This study examined the effect of whole-body vibration on pain and muscle elasticity in individuals with hyperlordosis and normal lordosis.
Flexible ruler for individuals' spinal curvatures (lumbar lordosis); back-lower back pain levels VAS; muscle elasticity Myoton Pro device; Physical functions will be evaluated with the Modified Oswestry low back pain scale.
Read the detailed description
This study examined the effect of whole-body vibration on pain and muscle elasticity in individuals with hyperlordosis and normal lordosis.
Flexible ruler for individuals' spinal curvatures (lumbar lordosis); back-lower back pain levels VAS; muscle elasticity Myoton Pro device; Physical functions will be evaluated with the Modified Oswestry low back pain scale.
The viscoelasticity properties ( tone, stiffness, elasticity) of the Musculus Trapezius and Musculus Pectoralis were assessed with MyotonPro® (Myoton AS, Estonia) during prone position on both sides.
Individuals will be divided into two groups: hyperlordosis and normal lordosis. Whole body vibration will be applied twice a week for six weeks, with a frequency of 30 Hz and an intensity of 2 mm.
A total of 28 females and males (14 individuals for each group) with hyperlordosis (>40°) and normal lordosis participated in the study.
- Conditions
- Lordosis; Postural, Lordosis, Hyperlordosis
- Being tested
- Whole body vibration
- Keywords
- Whole-body vibration, Lordosis, Hyperlordosis
- Medical subject headings
- Lordosis, Swayback
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Whole body vibrationOther
Whole body vibration will be applied while standing with a frequency of 30 Hz and an intensity of 2 mm by vibration machine
| Study group | Role | What they receive |
|---|---|---|
| LORDOSİS | Experimental | 30-40 Receives: Other: Whole body vibration |
| HYPERLORDOSİS | Experimental | 40< Receives: Other: Whole body vibration |
What is being measured
The primary outcome is the main question the study is designed to answer.
Muscle viscoelastic properties
muscle stiffness
Measured: 6 weeks
Secondary outcomes (1)
Pain level
Visual Analog Scale: between 0 -10 points; 0 (zero) no pain; 5 (five) Moderate pain; 10 (ten) Worst possible Pain
Measured: 6 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Jul 2024
- Study start5 Nov 2023
- Primary completion20 Apr 2024
- Study completion28 Jun 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Lordosis; PosturalStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Investigator
- Enrolment
- 28 participants (actual)
Sponsor and investigators
- Lead sponsor
- Gaziantep Islam Science and Technology University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Gönül Elpeze, Gaziantep Islam Science and Technology University
- Investigators
- Gonul Elpeze, Principal investigator, Gaziantep Islam Science and Technology University Physical Therapy and Rehabilitation Department
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06521983
- Sponsor's protocol ID
- GİBTU-GE-VİBRATİON
- Acronym
- WBV
- Status last verified
- Jul 2024
- First submitted
- 10 Jul 2024
- Last updated
- 30 Jul 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 30 Jul 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Whole Body Vibration on Pain and Muscle Elasticity in Individuals With Hyperlordosis and Normal Lordosis
- ClinicalTrials.gov ID
- NCT06521983
- Acronym / sponsor ID
- WBV / GİBTU-GE-VİBRATİON
- Conditions
- Lordosis; Postural, Lordosis, Hyperlordosis
- Keywords
- Whole-body vibration, Lordosis, Hyperlordosis
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 28 participants (actual)
- Lead sponsor
- Gaziantep Islam Science and Technology UniversityUniversity, hospital or other
- Study start
- 5 Nov 2023 (actual)
- Primary completion
- 20 Apr 2024 (actual)
- Study completion
- 28 Jun 2024 (actual)
- First posted
- 26 Jul 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study examined the effect of whole-body vibration on pain and muscle elasticity in individuals with hyperlordosis and normal lordosis.
Flexible ruler for individuals' spinal curvatures (lumbar lordosis); back-lower back pain levels VAS; muscle elasticity Myoton Pro device; Physical functions will be evaluated with the Modified Oswestry low back pain scale.
Detailed description
This study examined the effect of whole-body vibration on pain and muscle elasticity in individuals with hyperlordosis and normal lordosis.
Flexible ruler for individuals' spinal curvatures (lumbar lordosis); back-lower back pain levels VAS; muscle elasticity Myoton Pro device; Physical functions will be evaluated with the Modified Oswestry low back pain scale.
The viscoelasticity properties ( tone, stiffness, elasticity) of the Musculus Trapezius and Musculus Pectoralis were assessed with MyotonPro® (Myoton AS, Estonia) during prone position on both sides.
Individuals will be divided into two groups: hyperlordosis and normal lordosis. Whole body vibration will be applied twice a week for six weeks, with a frequency of 30 Hz and an intensity of 2 mm.
A total of 28 females and males (14 individuals for each group) with hyperlordosis (>40°) and normal lordosis participated in the study.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| LORDOSİS | Experimental | Other: Whole body vibration30-40 |
| HYPERLORDOSİS | Experimental | Other: Whole body vibration40< |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Being over 18 years of age,
- Having pain >5 according to VAS measurement,
- Having normal lumbar lordosis angle between 30°-40°,
- Having hyperlordosis angle >40°
Key exclusion criteria (3 listed)
- Having Scheurmann kyphosis, ,
- Having scoliosis (Cobb angle >10°),
- Having other congenital spine abnormalities
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Whole body vibrationWhole body vibration will be applied while standing with a frequency of 30 Hz and an intensity of 2 mm by vibration machine | Other | HYPERLORDOSİS, LORDOSİS |
Primary outcome
Muscle viscoelastic properties
Time frame: 6 weeks
muscle stiffness
1 secondary outcome
Pain level
Time frame: 6 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Jul 2024.
- Individual participant dataSharing planned: No
Related trials for Lordosis; Postural
Enrolling by invitation
Egoscue and Core Stabilization for Chronic Low Back Pain
Chronic Low Back Pain (CLBP)
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Gonul Elpeze principal investigator
Gaziantep Islam Science and Technology University Physical Therapy and Rehabilitation Department
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Whole body vibration in people with Lordosis; Postural and Lordosis, run by Gaziantep Islam Science and Technology University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 30 Jul 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Muscle viscoelastic properties (time frame: 6 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Jul 2024.