UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000055698 |
|---|---|
| Receipt number | R000063646 |
| Scientific Title | Verification of the effect of 4 weeks of trunk flexion training with whole body vibration on lumbar erector spinae muscle stiffness. |
| Date of disclosure of the study information | 2024/10/02 |
| Last modified on | 2024/10/02 09:33:39 |
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Basic information
Public title
Verification of the effect of 4 weeks of trunk training using a whole body vibration device on back muscle stiffness.
Acronym
Effects of 4 weeks of trunk training with whole body vibration on back muscle stiffness.
Scientific Title
Verification of the effect of 4 weeks of trunk flexion training with whole body vibration on lumbar erector spinae muscle stiffness.
Scientific Title:Acronym
Effects of 4 weeks of trunk flexion training with whole body vibration on erector spinae stiffness
Region
| Japan |
Condition
Condition
Healthy person
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To clarify whether or not whole body vibration has an effect on spinal erector stiffness reduction
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Erector spinae muscle stiffness
Key secondary outcomes
Pressure pain threshold, lumbar motion angle, lumbar proprioception
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Single blind -investigator(s) and assessor(s) are blinded
Control
Placebo
Stratification
YES
Dynamic allocation
NO
Institution consideration
Institution is not considered as adjustment factor.
Blocking
YES
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Device,equipment |
Interventions/Control_1
Whole body vibration
Interventions/Control_2
Non-Whole body vibration
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| 18 | years-old | <= |
Age-upper limit
| 30 | years-old | > |
Gender
Male and Female
Key inclusion criteria
healthy university student
Key exclusion criteria
1. those who have pain that interferes with their daily life
2. those who have typical physical dysfunction such as paralysis due to cerebrovascular disease
3. those with a history of surgery that significantly affects the movement of the spine or hip joint, such as spinal fusion or hip replacement surgery
4. those with significant deformity of the spine
5. those with cognitive decline
6. pregnant.
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | Ryo |
| Middle name | |
| Last name | Miyachi |
Organization
Hokuriku University
Division name
Faculty of Medical and Health Sciences
Zip code
9201180
Address
1-1 Taiyogaoka, Kanazawa, Ishikawa
TEL
0762291161
ry_miyachi@hokuriku-u.ac.jp
Public contact
Name of contact person
| 1st name | Ryo |
| Middle name | |
| Last name | Miyachi |
Organization
Hokuriku University
Division name
Faculty of Medical and Health Sciences
Zip code
9201180
Address
1-1 Taiyogaoka, Kanazawa, Ishikawa
TEL
0762291161
Homepage URL
ry_miyachi@hokuriku-u.ac.jp
Sponsor or person
Institute
Hokuriku University
Institute
Department
Personal name
Funding Source
Organization
Japan society for promotion of science
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Japan
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Hokuriku University
Address
1-1 Taiyogaoka, Kanazawa, Ishikawa
Tel
0762291161
ry_miyachi@hokuriku-u.ac.jp
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2024 | Year | 10 | Month | 02 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Preinitiation
Date of protocol fixation
| 2024 | Year | 10 | Month | 02 | Day |
Date of IRB
Anticipated trial start date
| 2024 | Year | 10 | Month | 07 | Day |
Last follow-up date
| 2024 | Year | 12 | Month | 19 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2024 | Year | 10 | Month | 02 | Day |
Last modified on
| 2024 | Year | 10 | Month | 02 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063646
