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Effects on frailty prevention when using home EMS equipment and health food intake for 12 weeks

Effects on frailty prevention when using home EMS equipment and health food intake for 12 weeks: single blinded study - Effects on frailty prevention when using home EMS equipment and health food intake for 12 weeks

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000054385
Enrollment
26
Registered
2024-05-14
Start date
2024-05-14
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

Use of equipment, consumption of test foods, and specific exercise for 12 weeks Life as usual for a certain period of time

Sponsors

Japan Clinical Trial Association
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Subjects who have discomfort or pain in the knee joint 2.Subjects who have difficulty in standing up smoothly or walking for long periods of time.

Exclusion criteria

Exclusion criteria: 1. Subjects who have a daily exercise routine/training 2. Subjects with a history of food allergies 3. Subjects who need assistance from others and are unable to walk independently 4. Subjects who are taking medicines that affect the test (e.g., knee joint pain, flail prevention, etc.) 5. who are in the hospital or taking prescription drugs 6. Who are undergoing treatment (hormone replacement therapy, drug therapy, or other) at a medical institution for the treatment or prevention of disease, or whose condition is judged to require treatment at the time consent is obtained. 7. Subjects have participated in any other human studies (all human studies using cosmetics, foods, pharmaceuticals, quasi-drugs, medical devices, etc.) within the past 4 weeks, or Subjects are scheduled to participate in any other human studies during the period when this study is scheduled to be conducted. 8. Other subjects deemed inappropriate by the study investigator.

Design outcomes

Primary

MeasureTime frame
Physical fitness measurement, muscle strength measurement, JOA score

Countries

Japan

Contacts

Public ContactTakeshi Kaneko

Japan Clinical Trial Association N.A.

info@yakujihou.org0364574666

Outcome results

None listed

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