UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000061539
Receipt number R000070419
Scientific Title A Survey of Satisfaction with Anma Massage and Shiatsu (Finger Pressure Therapy) Provided by Health Keepers for Asthenopia
Date of disclosure of the study information 2026/05/12
Last modified on 2026/05/12 16:08:20

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

A Survey of Satisfaction with Anma Massage and Shiatsu (Finger Pressure Therapy) Provided by Health Keepers for Eye Strain

Acronym

A Survey of Satisfaction with Anma Massage and Shiatsu (Finger Pressure Therapy) Provided by Health Keepers for Eye Strain

Scientific Title

A Survey of Satisfaction with Anma Massage and Shiatsu (Finger Pressure Therapy) Provided by Health Keepers for Asthenopia

Scientific Title:Acronym

A Survey of Satisfaction with Anma Massage and Shiatsu (Finger Pressure Therapy) Provided by Health Keepers for Asthenopia

Region

Japan


Condition

Condition

Asthenopia

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

This study aimed to evaluate workers' satisfaction with anma-shiatsu therapy provided by Health Keepers for asthenopia.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Satisfaction and Degree of Eye Strain

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Maneuver

Interventions/Control_1

anma-shiatsu therapy

Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

18 years-old <=

Age-upper limit

65 years-old >

Gender

Male and Female

Key inclusion criteria

1. Healthy individuals aged 18 to 64 at the time of consent
2. Individuals who report experiencing eye strain
3. Individuals who use digital devices for four or more hours per day

Key exclusion criteria

1. Individuals who are currently participating in (or plan to participate in) other studies or clinical trials during the same period
2. Individuals deemed ineligible for this study by the principal investigator or other researchers

Target sample size

35


Research contact person

Name of lead principal investigator

1st name Shogo
Middle name
Last name Miyazaki

Organization

Teikyo Heisei University

Division name

Faculty of Health Care

Zip code

1708445

Address

2-51-4 Higashiikebukuro, Toshima-ku, Tokyo

TEL

03-5843-3111

Email

s.miyazaki@thu.ac.jp


Public contact

Name of contact person

1st name Shogo
Middle name
Last name Miyazaki

Organization

Teikyo Heisei University

Division name

Faculty of Health Care

Zip code

1708445

Address

2-51-4 Higashiikebukuro, Toshima-ku, Tokyo

TEL

03-5843-3111

Homepage URL


Email

s.miyazaki@thu.ac.jp


Sponsor or person

Institute

Teikyo Heisei University

Institute

Department

Personal name



Funding Source

Organization

Teikyo Heisei University

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor

Cosmos Initia Co., Ltd.

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Teikyo Heisei University

Address

2-51-4 Higashiikebukuro, Toshima-ku, Tokyo

Tel

03-5843-3111

Email

rec@thu.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2026 Year 05 Month 12 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Preinitiation

Date of protocol fixation

2026 Year 04 Month 28 Day

Date of IRB

2026 Year 04 Month 28 Day

Anticipated trial start date

2026 Year 06 Month 01 Day

Last follow-up date

2026 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2026 Year 05 Month 12 Day

Last modified on

2026 Year 05 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070419