NCT06293196

Brief Summary

This study aims to investigate whether the acupoint eye exercise could impact the biological parameters of the eye.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
55

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started Sep 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress95%
Sep 2023Jun 2026

Study Start

First participant enrolled

September 1, 2023

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

February 1, 2024

Completed
1 month until next milestone

First Posted

Study publicly available on registry

March 5, 2024

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Last Updated

January 21, 2026

Status Verified

January 1, 2026

Enrollment Period

2.8 years

First QC Date

February 1, 2024

Last Update Submit

January 18, 2026

Conditions

Outcome Measures

Primary Outcomes (7)

  • The effect of ocular acupoint massage on ocular blood flow.

    Ocular blood flow indicators were obtained using Optical Coherence Tomography (OCT).

    Ocular blood flow indicators were measured once at pre-intervention, immediately post-intervention, and at 10, 20, and 30 minutes post-intervention.

  • The effect of ocular acupoint massage on intraocular pressure.

    Intraocular pressure (IOP) of patients was measured and recorded with the ICARE rebound tonometer.

    Intraocular pressure was measured once before the intervention and once immediately after the intervention.

  • The effect of ocular acupoint massage on the diameter of Schlemm's canal.

    Imaging of the nasal and temporal corneoscleral regions of the right eye was performed using swept-source anterior segment optical coherence tomography (SS-AS-OCT). The diameter of Schlemm's canal was measured manually.

    Anterior segment imaging was performed once before and once immediately after the intervention to obtain the diameter values of Schlemm's canal.

  • The effect of ocular acupoint massage on the area of Schlemm's canal.

    Imaging of the nasal and temporal corneoscleral regions of the right eye was performed using swept-source anterior segment optical coherence tomography (SS-AS-OCT). The area of Schlemm's canal was measured manually.

    Anterior segment imaging was performed once before and once immediately after the intervention to obtain the area values of Schlemm's canal.

  • The effect of ocular acupoint massage on the width of the trabecular meshwork.

    Imaging of the nasal and temporal corneoscleral regions of the right eye was performed using swept-source anterior segment optical coherence tomography (SS-AS-OCT). The width of the trabecular meshwork was measured manually.

    Anterior segment imaging was performed once before and once immediately after the intervention to obtain the width values of the trabecular meshwork.

  • The effect of ocular acupoint massage on the thickness of the trabecular meshwork.

    Imaging of the nasal and temporal corneoscleral regions of the right eye was performed using swept-source anterior segment optical coherence tomography (SS-AS-OCT). The thickness of the trabecular meshwork was measured manually.

    Anterior segment imaging was performed once before and once immediately after the intervention to obtain the thickness values of the trabecular meshwork.

  • The effect of ocular acupoint massage on the tear film.

    The Keratograph was used to dynamically monitor the tear film break-up location and break-up time in a non-contact manner before and after the intervention, with tear meniscus height measured manually.

    The Keratograph was performed once before the intervention and once immediately after the intervention.

Secondary Outcomes (2)

  • The effect of ocular acupoint massage on blood pressure.

    Blood pressure was measured once before the intervention and once immediately after it.

  • The effect of ocular acupoint massage on heart rate.

    Heart rate was measured once before the intervention and once immediately after it.

Study Arms (4)

standard Chinese acupoint eye exercise group

EXPERIMENTAL

The volunteers performed a set of standard Chinese acupoint eye health exercises.

Other: acupressure

fake acupoint eye exercise group

EXPERIMENTAL

Volunteers performed a group of fake acupoint eye health exercises, the acupoint design in the place without acupoints.

Other: acupressure

simple eye closure group

NO INTERVENTION

The volunteers only closed their eyes and did not perform acupressure.

simple distance observation group

NO INTERVENTION

The volunteers only looked far without acupressure.

Interventions

Massage acupoints and non-acupoint areas around the eyes.

fake acupoint eye exercise groupstandard Chinese acupoint eye exercise group

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • healthy people of all ages

You may not qualify if:

  • presence of systemic diseases
  • history of other eye diseases, surgeries, and/or medications, as well as eye trauma
  • incomplete healing of the surgical site after eye surgery
  • consumption of coffee, tea, or vasodilators within 6 hours before the commencement of the test

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Zhongnan Hospital of Wuhan University

Wuhan, Hubei, 430000, China

RECRUITING

MeSH Terms

Interventions

Acupressure

Intervention Hierarchy (Ancestors)

Therapy, Soft TissueMusculoskeletal ManipulationsComplementary TherapiesTherapeuticsPhysical Therapy ModalitiesRehabilitation

Central Study Contacts

Min Ke, doctor of medicine

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 1, 2024

First Posted

March 5, 2024

Study Start

September 1, 2023

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

June 30, 2026

Last Updated

January 21, 2026

Record last verified: 2026-01

Locations