UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000035808 |
|---|---|
| Receipt number | R000040793 |
| Scientific Title | The effects of diffrent density type foam rollers after intermittent exercise on range of motion, muscle damage, muscle soreness, muscle hardness, and muscle activation. |
| Date of disclosure of the study information | 2019/02/07 |
| Last modified on | 2020/01/05 13:03:47 |
* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments
Basic information
Public title
The effects of diffrent density type foam rollers after intermittent exercise on range of motion, muscle damage, muscle soreness, muscle hardness, and muscle activation.
Acronym
Diffrent density type foam rollers and recovery
Scientific Title
The effects of diffrent density type foam rollers after intermittent exercise on range of motion, muscle damage, muscle soreness, muscle hardness, and muscle activation.
Scientific Title:Acronym
Diffrent density type foam rollers and recovery
Region
| Japan |
Condition
Condition
Exericse induced fatigue
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The purpose of this study is to investigate the effect of diffrent density type of foam rollers on recovery after exercise induced fatigue.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Renge of motion, muscle hardness, muscle damage, muscle soreness, and muscle activation at Post-0, Post-20, Post-60, Post-24h, and Post-48 h.
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Randomized
Randomization unit
Individual
Blinding
Single blind -participants are blinded
Control
No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Device,equipment |
Interventions/Control_1
SMR using soft foam roller (1 min, 2 repetitions)
Interventions/Control_2
SMR using hard foam roller (1 min, 2 repetitions)
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
| 40 | years-old | > |
Gender
Male
Key inclusion criteria
1. Healthy men aged 18 to 40.
2. Maximal oxygen uptake is above 50 ml/kg/min
3. Healthy men who trained (i.e., more than an hour per session) for more than 2 days per week.
Key exclusion criteria
1. Men who have medical disease.
2. Men who have surgical disease.
3. Men who have mental illnesses.
Target sample size
16
Research contact person
Name of lead principal investigator
| 1st name | Norikazu |
| Middle name | |
| Last name | Hirose |
Organization
Waseda University
Division name
Faculty of Sport Sciences
Zip code
202-0021
Address
3-4-1 Higashihushimi, Nishitokyo, Tokyo, 202-0021, Japan
TEL
04-2451-1022
toitsu_hirose@waseda.jp
Public contact
Name of contact person
| 1st name | Takuma |
| Middle name | |
| Last name | Yanaoka |
Organization
Waseda university
Division name
Graduate School of Sport Sciences
Zip code
202-0021
Address
2-7-5-208 Higashihushimi, Nisitokyo, Tokyo, 202-0021, Japan
TEL
04-2461-1322
Homepage URL
takumayanaoka@toki.waseda.jp
Sponsor or person
Institute
Waseda Univerity
Institute
Department
Personal name
Funding Source
Organization
N/A
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
the Ethics Review Committee on Research with Human Subjects of Waseda University
Address
1-104, Totsuka, Shinjuku, Tokyo, Japan
Tel
+81-3-5272-1639
rinri@list.waseda.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
| 2019 | Year | 02 | Month | 07 | 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
10
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
Completed
Date of protocol fixation
| 2019 | Year | 02 | Month | 07 | Day |
Date of IRB
| 2019 | Year | 02 | Month | 18 | Day |
Anticipated trial start date
| 2019 | Year | 02 | Month | 20 | Day |
Last follow-up date
| 2019 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2019 | Year | 02 | Month | 07 | Day |
Last modified on
| 2020 | Year | 01 | Month | 05 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000040793
| Research Plan | |
|---|---|
| Registered date | File name |
| Research case data specifications | |
|---|---|
| Registered date | File name |
| Research case data | |
|---|---|
| Registered date | File name |
