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Acute Effects of Vibration on Shoulder Flexibility - Experimental Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02649452
Enrollment
40
Registered
2016-01-07
Start date
2015-11-30
Completion date
Unknown
Last updated
2016-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

Whole body Vibration

Brief summary

Whole body vibration (WBV) can help to improve muscle flexibility by stimulating the neuromuscular functions. But there is a dearth in the literature to prove its effectiveness in improving the flexibility of the upper limb muscles. Therefore the purpose of the study is to determine the effects of vibration on improving upper limb flexibility. This experimental research will be conducted by recruiting participants at the age of 19 to 27 with no histories of injuries on the upper limb. They will be randomly assigned into two groups; experimental (with vibration) and control (no vibration) group. The WBV machine will be used to provide vibration to the upper extremities by placing both palms on the vibration platform. The outcome measure of active chest flexibility and shoulder reach flexibility will be performed pre and post vibration.

Interventions

OTHERvibration

vibration will be given using whole body vibration machine. The subject will place both palms on top of the vibration platform with their knee supported on the ground. They need to apply as much pressure on the vibration platform by using their body weight. The whole body vibration machine will be set at the frequency of 30 Hz and the amplitude of 5 mm. They need to hold that position for 1 minute for 3 sets with 1 minute rest in between. The researcher will immediately stop this if the subjects feel dizziness and discomfort

Sponsors

Universiti Tunku Abdul Rahman
CollaboratorOTHER
Manisha Parai
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 27 Years
Healthy volunteers
Yes

Inclusion criteria

* ages of 19 to 28 * no athletic background

Exclusion criteria

* shoulder pain and injury within 12 months, recent back pain and neck pain, recent fever and high blood pressure.

Design outcomes

Primary

MeasureTime frame
Active Chest Flexibility testone minute
Shoulder Reach Flexibility testone minute

Countries

Malaysia

Contacts

Primary ContactManisha Parai, MPT
manisha@utar.edu.my0173128276

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026