Intervention Study on Dry Eye among office workers

Intervention Study on Dry Eye among office workers - Intervention Study on Dry Eye among office workers

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000010019

Enrollment

Registered

2013-02-12

Start date

2013-02-13

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

Dry Eye

Interventions

life style intervention Control

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Definitive Dry Eye Probable Dry Eye

Exclusion criteria

Exclusion criteria: People engaging in regular vigorous exercise or being on diet People under dry eye treatment including eyedrops and punctual plug Pregnant or lactating women Patients with either cataract or glaucoma Patients with serious cardiovascular, hepatic, or renal diseases Patients with malignant tumors Patients who participated in any clinical study within three month prior to signing the informed consent People whom the investigator or the subinvestigators consider to be ineligible for the intervention therapy judging from their medical history or general condition People whom the investigator or the subinvestigators consider to be ineligible for the intervention therapy in any other reason

Design outcomes

Primary

Measure	Time frame
Dry eye symptoms tear breakup time Schirmer test value cornea staining score	—

Countries

Japan

Contacts

Public ContactMotoko Kawashima

Keio University School of Medicine Ophthalmology

motoko326@gmail.com0353633866

Outcome results

None listed

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