| Recruitment status | Completed |
| Unique ID issued by UMIN | UMIN000037594 |
| Receipt No. | R000042847 |
| Scientific Title | The effect on muscle mass of health food :a randomized, double blind, placebo-controlled study |
| Date of disclosure of the study information | 2019/08/26 |
| Last modified on | 2020/04/15 (Ver. 5) |
| Basic information | ||
| Public title | muscle mass trial | |
| Acronym | muscle mass trial | |
| Scientific Title | The effect on muscle mass of health food :a randomized, double blind, placebo-controlled study | |
| Scientific Title:Acronym | muscle mass trial | |
| Region |
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| Condition | ||
| Condition | Healthy adult | |
| Classification by specialty |
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| Classification by malignancy | Others | |
| Genomic information | NO | |
| Objectives | |
| Narrative objectives1 | Compare the differences in muscle mass and body size between the group receiving HMB and protein-containing health food and the group not receiving it |
| Basic objectives2 | Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | |
| Assessment | |
| Primary outcomes | muscle mass, body size |
| Key secondary outcomes | subjective evaluation |
| 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 | Treatment | |
| Type of intervention |
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| Interventions/Control_1 | Ingestion of test article daily for 12 weeks | |
| Interventions/Control_2 | Ingestion of placebo article daily for 12 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 |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | 1. Subjects who is aware of muscle decline
2. Subjects who wants body makeup 3. Subjects who want to tighten their body 4. BMI 23 or more and less than 30 |
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| Key exclusion criteria | 1. Subject with a history of food allergy
2. Subject who are pregnant or nursing 3. Subjects taking health food that has effect 4. Subjects taking medication to bring about the effect |
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| Target sample size | 36 | |||
| Research contact person | |||||||
| Name of lead principal investigator |
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| Organization | Japan clinical trial assosiation | ||||||
| Division name | N.A. | ||||||
| Zip code | 1600022 | ||||||
| Address | 5F, 4-3-17 Shinjuku, Shinjukuku, Tokyo | ||||||
| TEL | 0364574666 | ||||||
| info@yakujihou.org | |||||||
| Public contact | |||||||
| Name of contact person |
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| Organization | Japan Clinical Trial Association | ||||||
| Division name | N.A. | ||||||
| Zip code | 1600022 | ||||||
| Address | 5F, 4-3-17 Shinjuku, Shinjukuku, Tokyo | ||||||
| TEL | 0364574666 | ||||||
| Homepage URL | |||||||
| info@yakujihou.org | |||||||
| Sponsor | |
| Institute | Japan clinical trial assosiation |
| Institute | |
| Department | |
| Funding Source | |
| Organization | EC STUDIO Co., Ltd. |
| 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 | Institutional Review Board of Pharmaceutical Law Wisdoms |
| Address | 5F, 4-3-17 Shinjuku, Shinjukuku, Tokyo |
| Tel | 0364574911 |
| master@yakujihou.net | |
| 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 |
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| Related information | |
| URL releasing protocol | |
| Publication of results | Published |
| Result | |
| URL related to results and publications | |
| Number of participants that the trial has enrolled | 26 |
| 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 |
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| Date of IRB |
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| Anticipated trial start date |
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| Last follow-up date |
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| Date of closure to data entry | |||||||
| Date trial data considered complete | |||||||
| Date analysis concluded | |||||||
| Other | |
| Other related information | |
| Management information | |||||||
| Registered date |
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| Last modified on |
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042847 |