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Exploratory study of flail prevention with ankle weight (AW) --Preliminary vertifiate examination and problem extraction in mounting

Exploratory study of flail prevention with ankle weight (AW) --Preliminary vertifiate examination and problem extraction in mounting - Exploratory study of flail prevention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038073
Enrollment
40
Registered
2019-09-21
Start date
2018-11-05
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

Healty volunteer

Interventions

In the intervention group, they can mount Ankle wight by their free will and record the installation time and the activity situation in the diary note. And wright down resistance to fit and health dam

Sponsors

Nagoya City University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Those who gathered to recruit volunteers by calling for areas, companies, administrative staff, facility residents, etc. 2) Motor Fitness Scale scores more than 60% of 14 points 3) Those who can wear a pedometer for 14 weeks and accurately respond to inquiries 4) A person who became an ankle weight intervention group selects its weight by self-responsibility, who can receive an activity description in the diary note every day through the wearing period of 6 weeks 5) Person who obtained document agreement from himself / herself

Exclusion criteria

Exclusion criteria: 1) Young people under the age of 50 2) Possible pregnancy or pregnancy 3) The person whome the Muscle strengthening agent used for doping etc., male hormone preparation, adult cortical hormone preparation in use (local topical application is not applicable) 4) MFS score is less than 60% of 14 points 5) Those who have spontaneous pain and exercise pain at the discretion of a doctor by listening to the presence or absence of joint pain, muscle pain, such as back pain / knee joint pain at the hearing 6) Those who have problems with radiation exposure (radiation exposure) for CT examination applicants (voluntary) 7) Others who judged that the research director is inappropriate

Design outcomes

Primary

MeasureTime frame
motor function By the comparison between the two groups (intervention group vs. non-intervention group) of the mean value of the duration (seconds) by single feet standing test with eye opning after the intervention (6 weeks).

Countries

Japan

Contacts

Public ContactEmiko Yoshino

Nagoya City University Hospital Community-based Integrated Care System Promotion and Research Center

yoshino@med.nagoya-cu.ac.jp052-853-8536

Outcome results

None listed

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