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Foot Reflexology in Ocular Hypertensive and Glaucoma Patients

Effect of Foot Reflexology on Intraocular Pressure in Ocular Hypertensive and Glaucoma Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04695314
Enrollment
27
Registered
2021-01-05
Start date
2017-11-07
Completion date
2020-11-18
Last updated
2021-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma, Ocular Hypertension

Brief summary

To determine the effect of foot reflexology in primary open angle glaucoma (POAG) patients and the effect of a shoe insert to perform continuous foot reflexology in ocular hypertensive (OHTN) patients.

Detailed description

This is a prospective pilot study in glaucoma patients and a prospective therapeutic trial in ocular hypertensive patients. Patients were recruited from the Temple Ophthalmology outpatient clinic. Primary open-angle glaucoma patients were recruited from those about to have SLT for additional intraocular pressure (IOP) lowering. OHTN patients were recruited from the clinic. The glaucoma patients performed a 5-minute foot massage on a foot massage board and the IOP was checked pre-massage, post-massage and 30, 60, 90 and 120 min post massage. OHTN patients underwent a one-month drop washout and then performed a 5-minute massage using a 3D-printed shoe insert with the identical pressure checks. They then were randomly assigned to wear the shoe insert or a sham insert for one day. IOP was checked before inserting the insert and at the end of the day. The number of steps was recorded each day.

Interventions

DEVICEMassage

Foot reflexology board (JAPAN TSUBO HH-700) with massage focused at the base of the second and third toes

PROCEDUREExperimental insert

Raised shoe insert, insert used for massage

PROCEDURESham insert

Flat shoe insert, insert used for massage

Sponsors

Temple University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
30 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

The inclusion criteria for this study in each study group are as follows. * Patients with ocular hypertension (age 30-90) who may or may not have been included in the original pilot study. * Patients with POAG (age 30-90) who are being asked to increase therapy to further lower their IOP. The

Exclusion criteria

for BOTH study groups will be: * Current participation in FR or other complementary and alternative medicine techniques who will not participate in a washout period. * Ocular hypotensive drop treatments for ocular-hypertension who will not participate in a washout period. * Previous eye surgery or laser treatment. * Physical inability to perform the tasks. Additional

Design outcomes

Primary

MeasureTime frameDescription
Intraocular Pressure Changes in Glaucoma PatientsCollect pressure readings for baseline, after 5 minutes of massage, and every 30 minutes for 2 hoursGlaucoma Patients
Intraocular Pressure Changes in Ocular Hypertensive PatientsCollect pressure readings for baseline, after 5 minutes of massage, and every 30 minutes for 2 hoursOcular Hypertensive Patients

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026