UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000057536 |
|---|---|
| Receipt number | R000065588 |
| Scientific Title | Comparison of the range of motion of hip joint in Subjects with transfemoral amputee in different floor sitting Position |
| Date of disclosure of the study information | 2025/05/23 |
| Last modified on | 2025/05/23 14:20:09 |
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Basic information
Public title
Comparison of the range of motion of hip joint in Subjects with transfemoral amputee in different floor sitting Position
Acronym
Comparison of the range of motion of hip joint in Subjects with transfemoral amputee in different floor sitting Position
Scientific Title
Comparison of the range of motion of hip joint in Subjects with transfemoral amputee in different floor sitting Position
Scientific Title:Acronym
Comparison of the range of motion of hip joint in Subjects with transfemoral amputee in different floor sitting Position
Region
| Japan |
Condition
Condition
transfemoral amputee
Classification by specialty
| Orthopedics | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To investigate changes in relative hip range of motion in subjects with and without transfemoral amputation in different floor sitting position.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Confirmatory
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
3D motion analysis device (VICON) will be used to measure range of motion of hip joint. All measurements will be obtained in deferent floor sitting position. Subjects will be asked to sit on the floor from standing position. The measurements of range of motion of hip joint will be compared between cross sitting position and side sitting position.
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Self control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Prevention
Type of intervention
| Other |
Interventions/Control_1
Subjects will be asked to move into either cross floor sitting position or floor side sitting position from standing position.
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
| 70 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Subjects with transfemoral amputation
Key exclusion criteria
a history of orthopedic surgery, immunological diseases (rheumatism, etc.), and neurological symptoms of the lower extremities on non-amputee side.
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | masaru |
| Middle name | |
| Last name | kanda |
Organization
niigata university of health and welfare
Division name
Dept. of Prosthetics, Orthotics and Assistive Technology
Zip code
9503198
Address
1398 shimai, Kita-ku, Niigata, Niigata, Japan
TEL
0252574621
kanda@nuhw.ac.jp
Public contact
Name of contact person
| 1st name | masaru |
| Middle name | |
| Last name | kanda |
Organization
Niigata University of Health and Welfare
Division name
Dept. of Prosthetics, Orthotics and Assistive Technology
Zip code
9503198
Address
1398 shimai, Kita-ku, Niigata, Niigata, Japan
TEL
0252574621
Homepage URL
kanda@nuhw.ac.jp
Sponsor or person
Institute
Niigata University of Health and Welfare
Institute
Department
Personal name
Funding Source
Organization
Niigata University of Health and Welfare
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Niigata University of Health and Welfare
Address
1398 shimai, Kita-ku, Niigata, Niigata, Japan
Tel
0252574621
kanda@nuhw.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
| 2025 | Year | 05 | Month | 23 | 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
| 2025 | Year | 03 | Month | 01 | Day |
Date of IRB
Anticipated trial start date
| 2025 | Year | 04 | Month | 30 | Day |
Last follow-up date
| 2026 | Year | 01 | 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
| 2025 | Year | 04 | Month | 07 | Day |
Last modified on
| 2025 | Year | 05 | Month | 23 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000065588
