Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
45 participants
INTERVENTIONAL
2018-06-06
2018-11-15
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
OTHER
DOUBLE
Study Groups
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63 Hz vibration group
Vibration of 63 Hz frequency was applied.
63 Hz Vibration
Vibrations of 63 Hz were applied with handheld vibration device.
42 Hz vibration group
Vibration of 42 Hz frequency was applied.
42 Hz Vibration
Vibrations of 42 Hz were applied with handheld vibration device.
Sham vibration group
No actual vibration was applied.
Sham vibration
Handheld device was applied to the participants without any vibrations.
Interventions
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63 Hz Vibration
Vibrations of 63 Hz were applied with handheld vibration device.
42 Hz Vibration
Vibrations of 42 Hz were applied with handheld vibration device.
Sham vibration
Handheld device was applied to the participants without any vibrations.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* history of sensory deficits in the upper extremity
* recent upper extremity injury
* undergoing any resistance training
19 Years
30 Years
MALE
Yes
Sponsors
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King Saud University
OTHER
Responsible Party
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Masood Khan
Principal Investigator
Principal Investigators
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Masood Khan, M.P.Th
Role: PRINCIPAL_INVESTIGATOR
King Saud University
Locations
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King Saud University
Riyadh, , Saudi Arabia
Countries
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Other Identifiers
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RRC-2018-007
Identifier Type: -
Identifier Source: org_study_id
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