Skip to content

Clinical Study for the Evaluation of the Effects of Test Food Consumption on Walking Function

Clinical Study for the Evaluation of the Effects of Test Food Consumption on Walking Function - Clinical Study for the Evaluation of the Effects of Test Food Consumption on Walking Function

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000061495
Enrollment
60
Registered
2026-05-11
Start date
2026-05-11
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adult

Interventions

One packet of the test food daily for 12 weeks One packet of placebo food daily for 12 weeks

Sponsors

EP Mediate Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Healthy men and women aged 50 to 75 years (2) Subjects with age-related declines in walking ability (3) Person who can understand the purpose and content of this study and agree in this study

Exclusion criteria

Exclusion criteria: (1) Subjects with diseases that may affect the study evaluation, or a history of such conditions (2) Subjects who experience severe knee or lower-back pain that interferes with daily activities or walking (3) Subjects who continuously consume health foods related to joints or muscles (4) Subjects who engage in strenuous exercise that places stress on the joints (5) Subjects who regularly engage in activities that may affect the evaluation of efficacy (6) Subjects who may develop allergies in relation to the study (7) Subjects with conditions requiring continuous medication those currently under treatment , or those with a history of serious illnesses requiring pharmacological treatment (8) Subjects with serious neurological diseases, malignant tumors, diabetes, liver, kidney, or heart diseases, or a history of such conditions (9) Subjects with current or past psychiatric disorders, or those strongly suspected of having such conditions (10) Subjects with markedly abnormal anthropometric, physical, or clinical test values prior to intake (11) Subjects with irregular lifestyles such as shift work or night work (12) Subjects with participation in another clinical study within the past month (13) Subjects who plan to become pregnant or breastfeed during the study period (14) Subjects who are judged to be unsuitable as subjects based on the answers to the background survey (15) Subjects who are judged as unsuitable for the study by the principal investigator or the investigator for other reason

Design outcomes

Primary

MeasureTime frame
6-minute walking distance

Secondary

MeasureTime frame
JKOM score, Grip strength, Timed Up and Go (TUG) test, 5 times sit-to-stand test, VAS (Visual Analog Scale)

Countries

Japan

Contacts

Public ContactChiharu Goto

EP Mediate Co., Ltd. Development Department Trial Planning Section

goto.chiharu069@eps.co.jp090-1536-4583

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026