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Clinical Trials/jRCT1070210063
jRCT1070210063RecruitingNot Applicable

Subjective estimation by range finder

University of the Ryukyus0 sites15 target enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
15
Primary Endpoint
-
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Single Arm Study
Intervention Model
Single Assignment
Primary Purpose
Health Services Research
Masking
Open(masking Not Used)

Eligibility Criteria

Ages
No limit to No limit (—)
Sex
All

Inclusion Criteria

  • •I am involved in VDT work on a daily basis.

Exclusion Criteria

  • •If you have a heart or mental illness, or have any other serious illness.
  • •There is an injury or illness for which treatment and rehabilitation have not been completed.
  • •You may be pregnant or you may be pregnant.
  • •It is skin atopy.
  • •In addition, when the practitioner judges that it is not suitable for the experiment.

Outcomes

Primary Outcomes

-

Subjective estimation accuracy

Secondary Outcomes

No secondary outcomes reported

Investigators

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