Skip to content

Pilot study for a randomized controlled trial on the actual condition of walking and improvement through instruction

Pilot study for a randomized controlled trial on the actual condition of walking and improvement through instruction - Pilot study of actual conditions of walking and improvement through instruction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000050621
Enrollment
10
Registered
2023-03-18
Start date
2023-03-18
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

None

Interventions

Sponsors

Showa Pharmaceutical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Students currently enrolled at Showa Pharmaceutical University who meet all of the following criteria: Age between 18 and 40 years old on the date consent is obtained. Persons who have obtained the subject's written consent to participate in this study.

Exclusion criteria

Exclusion criteria: People with hypersensitivity to the materials in the Walking Impact Analysis System (Safety Walk Navi) and the rise test box. People with pain, swelling, inflammation, injury, or paralysis of the lower limbs and with limited ambulation. People who cannot be fitted with the Safety Walk Navi device. Persons who are otherwise deemed unsuitable as subjects by the principal investigator.(Keep a record of the reasons for exclusion.)

Design outcomes

Primary

MeasureTime frame
Overall score of average acceleration with safety walk navigation system

Secondary

MeasureTime frame
Posture when standing and walking Average acceleration and score of up/down, left/right front by safety walk navigation system

Countries

Japan

Contacts

Public ContactChigusa Kikuchi

Showa Pharmaceutical University Department of Community Medicine, Center for Clinical Pharmacy Education and Research

c-kikuchi@ac.shoyaku.ac.jp+81-42-721-1535

Outcome results

None listed

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