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Visual ADL Research

Visual ADL Research - Visual ADL Research

Status
Active, not recruiting
Phases
Unknown
Study type
Unknown
Source
JPRN
Registry ID
JPRN-UMIN000041025
Enrollment
Unknown
Registered
2020-07-08
Start date
2020-01-01
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 listed

Interventions

None listed

Sponsors

Ministry of Health, Labor and Welfare
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Cases of Japanese males and females aged 20 to less than 65 and who meet each of the following conditions: 1) One eye group: Those who have an eyeball fistula or corrected vision of 0.02 or less in one eye and do not meet the criteria for recognition of visual impairment of persons with physical disabilities (the criteria after the revision in July 2018) (that is, correction of the other eye) Patients with visual acuity of 0.7 or more) 2) Blepharospasm group: Blepharospasm severity classification Grade 3 to 5 eyelid convulsions, but those who do not meet the criteria for recognition of visual impairment of the physically disabled and patients in the stable period after treatment. 3) Control group: A person who meets the 6th grade of the certification criteria for the physically handicapped person with visual impairment, or a visually impaired person (regardless of the name of eye disease) who falls under the 6th certification criteria.

Exclusion criteria

Exclusion criteria: Those who meet any of the following conditions are not eligible. 1) New patient 2) Those with significant changes in symptoms and findings 3) Since it is a visual impairment-related ADL survey, it is handicapped, deaf, dementia, etc., and if a substitute is required for a deputy 4) Those who have obtained a certificate of the physically disabled other than visually impaired 5) Those who cannot understand the content and procedures of this research 6) Those who are participating in other research 7) Persons who have difficulty visiting the hospital 8) In addition, those who are judged to be ineligible to carry out this research safely by the principal investigator or researchers.

Design outcomes

Primary

MeasureTime frame
The post-rush conversion scores of LVFDL and LVADL as LVFAM for activities of daily living of the visually impaired. Comparison is made between the one-eye group and the control group, and the blepharospasm group and the control group, respectively.

Countries

Japan

Contacts

Public ContactHirotaka Yokouchi

Chiba University Graduate School of Medicine Ophthalmology

yokouchi123@peace.ocn.ne.jp043-226-2124

Outcome results

None listed

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