Study Results
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Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2025-03-05
2025-04-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Placebo Vibration Group
In addition to the conventional treatment program, the placebo plantar vibration application will be applied to the plantar region of the patients in the placebo group. For the application, the local vibration device will be moved without touching the patient's skin while it is operational. The placebo plantar vibration will be applied for 30 minutes each day over 3 consecutive days.
Placebo Plantar Vibration
The patients in the placebo group will receive placebo plantar vibration intervention with a frequency of 100 Hz on the affected plantar region, without touching the skin, for 30 minutes each day over 3 consecutive days.
Local Vibration Intervention Group
In addition to the conventional treatment program, the patients in this group will receive plantar vibration application on the affected plantar region, utilizing a frequency of 100 Hz. The plantar vibration will be applied for 30 minutes each day over 3 consecutive days.
Plantar Vibration
The patients in the study group will receive plantar vibration intervention with a frequency of 100 Hz on the affected plantar region for 30 minutes each day over 3 consecutive days.
Interventions
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Plantar Vibration
The patients in the study group will receive plantar vibration intervention with a frequency of 100 Hz on the affected plantar region for 30 minutes each day over 3 consecutive days.
Placebo Plantar Vibration
The patients in the placebo group will receive placebo plantar vibration intervention with a frequency of 100 Hz on the affected plantar region, without touching the skin, for 30 minutes each day over 3 consecutive days.
Eligibility Criteria
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Inclusion Criteria
2. A Mini-Mental State Examination score of 24 or higher,
3. Being between 45 and 75 years of age,
4. Having a Brunnstrom stage of 4 or above,
5. Ability to stand independently for 20 seconds or more,
6. Ability to walk independently for 10 meters, using assistive devices or orthoses if necessary.
Exclusion Criteria
2. The presence of cancer or diabetic neuropathy,
3. The presence of vestibular disorder,
4. The presence of lower extremity ulceration or amputation,
5. Hemodynamic instability,
6. The presence of other neurological disorders (such as multiple sclerosis, Parkinson's disease),
7. Having experienced an acute lower extremity injury in the last six weeks,
8. History of lower extremity surgery,
9. Alcohol consumption in the last 24 hours
10. Posterior circulation stroke involving the basilar artery or cerebellum
45 Years
75 Years
ALL
No
Sponsors
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Bitlis Eren University
OTHER
Responsible Party
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Omer Dursun
Asst. Prof.
Principal Investigators
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ömer dursun, Asst. Prof.
Role: PRINCIPAL_INVESTIGATOR
Bitlis Eren University
burak mavuş, M.Sc.
Role: PRINCIPAL_INVESTIGATOR
Bolu Abant İzzet Baysal Physiotherapy and Rehabilitation Training and Research Hospital
Locations
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Bolu İzzet Baysal Fizik Tedavi ve Rehabilitasyon Eğitim ve Araştırma Hastanesi
Bolu, Merkez, Turkey (Türkiye)
Countries
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References
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Onal B, Karaca G, Sertel M. Immediate Effects of Plantar Vibration on Fall Risk and Postural Stability in Stroke Patients: A Randomized Controlled Trial. J Stroke Cerebrovasc Dis. 2020 Dec;29(12):105324. doi: 10.1016/j.jstrokecerebrovasdis.2020.105324. Epub 2020 Sep 28.
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Toosizadeh N, Wahlert G, Fain M, Mohler J. The effect of vibratory stimulation on the timed-up-and-go mobility test: a pilot study for sensory-related fall risk assessment. Physiol Res. 2020 Aug 31;69(4):721-730. doi: 10.33549/physiolres.934451. Epub 2020 Jul 16.
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Other Identifiers
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BEUFTR-7
Identifier Type: -
Identifier Source: org_study_id
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