The Reflex Mechanism Underlying Neuromuscular Effects Of The Whole Body Vibration (WBV-IRM)
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| ClinicalTrials.gov Identifier: NCT04516798 |
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Recruitment Status :
Completed
First Posted : August 18, 2020
Last Update Posted : October 27, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Reflex, Ankle, Decreased | Other: vibration | Not Applicable |
A total of eight volunteers were included according to the inclusion and exclusion criteria. The subjects were vibrated while standing upright with the WBV device (PowerPlate® Pro5). The 30, 35 and 40 Hz WBVs were applied for thirty seconds for each frequency with an amplitude of 2 mm. In the same session, 100, 135 and 150 Hz local vibrations were applied to the right Achilles tendon for thirty seconds for each frequency. 100, 135 and 150 Hz local vibrations were then applied to the right heel for thirty seconds for each frequency with an interval of five seconds. Vibration stimuli were recorded accelerometers. Reflex muscle responses were recorded from the right soleus muscle at a sampling rate of 40 KHz. Recording electrodes were placed on the belly of the right soleus muscle and the ground electrode was placed on the right medial malleolus.
The data were recorded with the PowerLab device, the records were processed and analyzed offline from the LabChart program. After the EMG records are filtered and rectified, reflex latencies were measured by cumulative averaging method using the accelerometer records as triggers (Karacan I, Cakar HI, Sebik O, Yilmaz G, Cidem M, Kara S, Türker KS.A new method to determine reflex latency induced by high rate stimulation of the nervous system.Front Hum Neurosci.2014 Jul 18; 8: 536.doi: 10.3389 / fnhum.2014.00536). After determining the Achilles tendon vibration reflex latency and the reflex latency induced by WBV, it was compared with statistical methods.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 8 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Intervention Model Description: | Self controlled experimental study |
| Masking: | None (Open Label) |
| Primary Purpose: | Basic Science |
| Official Title: | The Reflex Mechanism Underlying The Neuromuscular Effects Of The Whole Body Vibration |
| Actual Study Start Date : | October 5, 2020 |
| Actual Primary Completion Date : | October 7, 2020 |
| Actual Study Completion Date : | October 7, 2020 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Experiment
Local and whole body vibration were applied
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Other: vibration
local and whole-body vibration were applied |
- reflex latency [ Time Frame: during intervention, an average of 8 minutes ]The time between the vibration stimulus and the reflex muscle response triggered by it was defined as the latency.
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| Ages Eligible for Study: | 20 Years to 40 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Healthy
- Young adult (20-40 years old)
- Both gender
- Volunteer
Exclusion Criteria:
- Cardiac disorder (Rhythm / conduction disorder, Cardiac pacemaker, Ischemic heart disease)
- Finding or suspected active deep vein thrombosis,
- History of deep vein thrombosis and pulmonary embolism,
- Orthostatic hypotension
- Hypertension
- Presence of fracture in the lower limb
- Achilles Contractures
- Active inflammatory, rheumatological or infectious disease in the lower limb
- Peripheral nerve lesions such as polyneuropathy, radiculopathy in the lower limb
- Those with a history of Achilles tendinopathy / bursitis
- Those with a history of kidney stones
- Patients with dizziness and balance problems,
- Cases with lesions on the skin surface where electrodes were attached
- Those with communication-cooperation problems
- Having a history of panic attacks
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04516798
| Turkey | |
| Istanbul Physical Medicine Rehabilitation Training & Research Hospital | |
| İstanbul, Turkey, 34173 | |
| Principal Investigator: | Ilhan Karacan, Assoc Prof | Istanbul Physical Medicine Rehabilitation Training & Research Hospital |
| Responsible Party: | Istanbul Physical Medicine Rehabilitation Training and Research Hospital |
| ClinicalTrials.gov Identifier: | NCT04516798 |
| Other Study ID Numbers: |
ISTANBULPMR |
| First Posted: | August 18, 2020 Key Record Dates |
| Last Update Posted: | October 27, 2020 |
| Last Verified: | October 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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whole body vibration tonic vibration reflex muscle spindle |
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Reflex, Abnormal Neurologic Manifestations Nervous System Diseases |

