UMIN-CTR Clinical Trial

Recruitment status Completed
Unique ID issued by UMIN UMIN000017196
Receipt No. R000019952
Official scientific title of the study The effects of load rate and walking speed during anti-gravity treadmill walking on the oxygen uptake and the heart rate
Date of disclosure of the study information 2015/04/20
Last modified on 2018/11/27 (Ver. 5)

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Basic information
Official scientific title of the study The effects of load rate and walking speed during anti-gravity treadmill walking on the oxygen uptake and the heart rate
Title of the study (Brief title) The effects of load rate and walking speed during anti-gravity treadmill walking on the oxygen uptake and the heart rate
Region
Japan

Condition
Condition Healthy subjects
Classification by specialty
Adult
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 The porpose of this study is to investigate the effects of load rate and walking speed during anti-gravity treadmill walking on the oxygen uptake and the heart rate in the healthy subjects.
Basic objectives2 Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes the oxygen uptake during anti-gravity treadmill walking
Key secondary outcomes the heart rate during anti-gravity treadmill walking

Base
Study type Interventional

Study design
Basic design Single arm
Randomization Non-randomized
Randomization unit
Blinding Open -no one is blinded
Control Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms 1
Purpose of intervention Prevention
Type of intervention
Device,equipment
Interventions/Control_1 anti-gravity treadmill walking
Interventions/Control_2
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
20 years-old <=
Age-upper limit
29 years-old >=
Gender Male and Female
Key inclusion criteria healthy subjects
Key exclusion criteria The subject with previous history of orthopedic surgery.
The subject with neurological,cardiovascular and respiratory disease.
The subject who principal investigator has determined to be inappropriate.
Target sample size 20

Research contact person
Name of lead principal investigator Takeshi Chiba
Organization Hokkaido University Hosptal
Division name rehabilitation
Address Kita 14 Nishi 5, Kitaku, Sapporo, Hokkaido, Japan
TEL 011-706-5740
Email pt-chiba@med.hokudai.ac.jp

Public contact
Name of contact person Naoko Kojima
Organization Hokkaido University Hosptal
Division name rehabilitation
Address Kita 14 Nishi 5, Kitaku, Sapporo, Hokkaido, Japan
TEL 011-706-5740
Homepage URL
Email pt-koji@med.hokudai.ac.jp

Sponsor
Institute Hokkaido University Hosptal
Institute
Department

Funding Source
Organization no
Organization
Division
Category of Funding Organization Self funding
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

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
2015 Year 04 Month 20 Day

Progress
Recruitment status Completed
Date of protocol fixation
2013 Year 12 Month 10 Day
Anticipated trial start date
2013 Year 12 Month 10 Day
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Related information
URL releasing protocol
Publication of results Partially published
URL releasing results
Results
Other related information

Management information
Registered date
2015 Year 04 Month 20 Day
Last modified on
2018 Year 11 Month 27 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000019952