Healthy adults
Conditions
Interventions
Take food twice a day for 12 weeks.
Sponsors
DeNA Life Science, Inc
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Healthy volunteers (female/male), 30-50 age (time of informed consent) (2) Subjects obtained consent of participate DLS conducted research with data and samples through "MYCODE" DTC genetic test service. (3) Subjects obtained written consent intend to participate actively with well understanding with this study. (4) Subjects who can visit to the designated study date and participate in the study (5) Those who exercise at least once a week on a daily basis and can continue to exercise at least once a week during the test period. (6) Those who can cooperate with the dietary survey using the dietary survey application using a smartphone (record a total of 12 days within the test period). (7) Approximately 5-6 participants will be selected for each of the following categories from a) to f). a) Those who currently intake protein habitually, are conscious of the need to increase body muscle mass, and have a habit of resistance training at a gym at least twice a week. b) Those other than a) who currently intake protein on a habitual basis and have a desire to increase muscle mass. c) Those who currently intake protein habitually and want to reduce body fat mass and weight. d) Those who do not currently intake protein, but are interested in consuming protein and wish to increase their body muscle mass. e) Those who do not currently consume protein, but are interested in consuming protein and want to reduce body fat and weight. f) Those who do not currently consume protein and are not interested in consuming protein.
Exclusion criteria
Exclusion criteria: (1) Those who have withdrawn their consent to participate in this study for their own reasons. (2) Those who have a chronic medical condition that requires medication, those who have a history of serious illness that requires medication, or those who use pacemakers or other implantable medical electronic devices. (3) Those who may have allergic symptoms to the test food, or those who may have serious allergic symptoms to other foods or medicines. (4) Those who are pregnant, breastfeeding or may become pregnant. (5) Those who have participated in other clinical trials or monitoring studies in the last month, or those who plan to participate in other clinical trials or monitoring studies during this study period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1)Body weight, body composition (body fat mass and body muscle mass) 2)Amount and type of protein intake and exercise (type, intensity, duration) | — |
Secondary
| Measure | Time frame |
|---|---|
| 3)Physical condition, mood, awareness and behavior toward protein intake, exercise, diet, and body shape 4)Nutritional intake status | — |
Countries
Japan
Contacts
Public ContactHitomi Akio
DeNA Life Science, Inc MYCODE service Dept
Outcome results
None listed