UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000059123 |
|---|---|
| Receipt number | R000067633 |
| Scientific Title | A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on abdominal skeletal muscle mass and quality in women. |
| Date of disclosure of the study information | 2026/05/30 |
| Last modified on | 2025/09/18 16:11:23 |
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Basic information
Public title
A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on abdominal skeletal muscle mass and quality in women.
Acronym
A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on abdominal skeletal muscle mass and quality in women.
Scientific Title
A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on abdominal skeletal muscle mass and quality in women.
Scientific Title:Acronym
A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on abdominal skeletal muscle mass and quality in women.
Region
| Japan |
Condition
Condition
Healthy adults
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Evaluation of the effects of resistance training combined with supplementation of functional food ingredient on abdominal skeletal muscle mass and quality in women
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Abdominal muscle thickness at 8 weeks
Key secondary outcomes
Abdominal muscle thickness at 4 weeks
Abdominal muscle echo intensity, abdominal muscle strength, body composition, index of posture
Abdominal muscle mass at 8 weeks (assessed by MRI)
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Double blind -all involved are blinded
Control
Placebo
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Prevention
Type of intervention
| Food |
Interventions/Control_1
Intake of test food containing lemon myrtle extract for 8 weeks combined with resistance training for 8 weeks.
Interventions/Control_2
Intake of test food not containing lemon myrtle extract for 8 weeks combined with resistance training for 8 weeks.
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
| 30 | years-old | <= |
Age-upper limit
| 59 | years-old | >= |
Gender
Female
Key inclusion criteria
1.Subjects who are healthy women aged 30 to 59
2.Subjects with a BMI ranging from 18.5 to less than 30.0
3.Subjects who are aware of worse of abdominal muscles or getting increase of abdominal fat
Key exclusion criteria
1.Subjects who regularly engage in resistance training or endurance exercises
2.Subjects who regularly attend fitness facilities, including yoga or pilates classes
3.Subjects who have symptoms that interfere with training, such as lower back pain or arthralgia
4.Subjects who are currently on a diet involving dietary restrictions or similar weight-loss efforts
5.Subjects who have undergone, or plan to undergo, cosmetic medicine for weight loss, such as liposuction, medication, or injections
6.Subjects who take functional foods or supplements in order to improve of symptoms related to muscle or arthrosis on a daily basis
7.Subjects who have participated in clinical trials with exercises within the past year, or clinical trials with intake of pharmaceuticals or food ingredients within the past three month
8.Subjects who are considerably undernutrition
9.Subjects who are currently pregnant
10.Subjects who are judged to be ineligible by a doctor.
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | Shuichi |
| Middle name | |
| Last name | Machida |
Organization
Juntendo University
Division name
Graduate School of Health and Sports Science
Zip code
270-1695
Address
1-1 Hirakagakuendai, Inzai, Chiba 270-1695, Japan
TEL
0476-98-1001
machidas@juntendo.ac.jp
Public contact
Name of contact person
| 1st name | Shuichi |
| Middle name | |
| Last name | Machida |
Organization
Juntendo University
Division name
Graduate School of Health and Sports Science
Zip code
270-1695
Address
1-1 Hirakagakuendai, Inzai, Chiba 270-1695, Japan
TEL
0476-98-1001
Homepage URL
machidas@juntendo.ac.jp
Sponsor or person
Institute
Juntendo University
Institute
Department
Personal name
Funding Source
Organization
KANEKA CORPORATION
Organization
Division
Category of Funding Organization
Profit organization
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Ethics committee in Juntendo University Graduate School of Health and Sports Science
Address
1-1 Hirakagakuendai, Inzai, Chiba 270-1695, Japan
Tel
0476-98-1001
sc-rinri@juntendo.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
| 2026 | Year | 05 | Month | 30 | 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 | 08 | Month | 01 | Day |
Date of IRB
| 2025 | Year | 08 | Month | 01 | Day |
Anticipated trial start date
| 2025 | Year | 10 | Month | 01 | Day |
Last follow-up date
| 2026 | Year | 01 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
| 2026 | Year | 01 | Month | 31 | Day |
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2025 | Year | 09 | Month | 18 | Day |
Last modified on
| 2025 | Year | 09 | Month | 18 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000067633
