Accommodative Behaviors in Multifocal Contact Lenses

Sponsor
Ohio State University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06064617
Collaborator
(none)
20
1
2
15
1.3

Study Details

Study Description

Brief Summary

Soft multifocal contact lenses are used for a variety of reasons in patient care. Multifocal contact lenses are most often used to correct presbyopic vision by providing a range of clear vision at both distance and near. Multifocal contact lenses correct vision at different distances by introducing a power gradient over the eye. They are designed using center near or center distance designs. For center near designs, the near addition is place in the center of the lens, and the power becomes more negative in the periphery. Conversely, for center distance designs, the distance prescription is placed in the center, and the power of the lens becomes more positive in the periphery in order to provide the near addition. Center near and distance designs have varying advantages and disadvantages for presbyopic vision correction, so a fitter may choose a specific design based on a patient's individual visual needs. Generally, it is thought that center near designs provide the most accommodative relief and superior near vision because the near addition is centered in the pupil and able to allow maximum near correction, even with miotic pupil size changes associated with accommodation.

Plus lenses, or add powers, in spectacles are often used in the management of accommodative and binocular vision disorders. An add power, or plus lens, relieves accommodative demand. There is conflicting evidence on whether the add power in soft multifocal contact lenses can be used to manage accommodative and binocular vision disorders. Some case reports demonstrate benefits of multifocal contact lenses in accommodative insufficiency and convergence excess but the evidence is not clear and many previous studies utilize lenses that are not readily used anymore. Studies show that soft multifocal contact lenses alter accommodation in participants who wear lenses, but most studies use enter-distance lens designs, which is the most commonly used lens for myopia management.

Most studies that have evaluated accommodative ability and function while wearing soft multifocal contact lenses have examined center distance lenses. Because center distance lenses are used for myopia management, the interest has been to determine if children maintain normal accommodative function while wearing the lenses. Accommodative function while wearing center near lenses has likely not been studied often because these lens designs are used most in presbyopic populations who have no or waning accommodative ability and are using the lenses, specifically, to account for that accommodative inability.-Knowing how spectacle lenses with add powers effectively treat some binocular vision and accommodative disorders and understanding how center near multifocal contact lenses correct presbyopic vision, it is reasonable to hypothesize that center near multifocal contact lenses may provide a greater therapeutic effect for accommodative and binocular vision disorders than center near designs because the central portion of the lens is the addition power, unlike the center-distance lens designs. This study will aim to determine how accommodative function varies with center distance and center near multifocal contact lenses.

Condition or Disease Intervention/Treatment Phase
  • Device: Contact Lens
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
This study will be an observational single-center investigation using a cross sectional design and each subject will undergo two test sessions and will wear two different contact lenses.This study will be an observational single-center investigation using a cross sectional design and each subject will undergo two test sessions and will wear two different contact lenses.
Masking:
Single (Participant)
Masking Description:
Participants will not know what lens they are in
Primary Purpose:
Treatment
Official Title:
Accommodative Behaviors in Multifocal Contact Lenses
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Dec 31, 2024
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Center Distance Multifocal Contact Lens

All participants will wear a Biofinity center distance multifocal contact lens with a +2.50 add and measurements will be obtained.

Device: Contact Lens
Coopervision Biofinity Multifocal Lens

Experimental: Center Near Multifocal Contact Lens

All participants will wear a Biofinity center near multifocal contact lens with a +2.50 add and measurements will be obtained.

Device: Contact Lens
Coopervision Biofinity Multifocal Lens

Outcome Measures

Primary Outcome Measures

  1. Objective Accommodative Outcome [Up to two hours]

    Accommodative function will be compared using the Grand Seiko Autorefractor between the center distance and center near group. The instrument will record the patient's refractive error at distance and near (100 cm, 40 cm, and 25 cm)

Secondary Outcome Measures

  1. Accommodation Clinical Measures [Up to two hours]

    Accommodation will be assessed with monocular estimation method which is done with a clinical retinoscope, accommodative facility which uses lenses to determine how many times a patient can clear a target in one minute, and monocular accommodative push ups which is measured by bringing a reading target close to the eye and the patient reports when the target gets blurry. These eye focusing tests and outcomes will be compared in center distance and center near multifocal contact lens designs.

  2. Vergence Clinical Measures [Up to two hours]

    Vergence measures will be completed by checking cover test, which an examiner determines eye posture with a cover paddle and a near target. Modified Thorington will be assessed at distance and near, which is a card with a light in the center. The patient holds up a red lens over their eye and they report where they see the line crossing the cards.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 30 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Ages 18 to ≤ 30 years old

  • Acuity of 20/25 or better in both eyes with habitual contact lens prescription

  • No history of ocular disease or active ocular inflammation

  • No history of ocular or refractive surgery

  • No current history of rigid contact lens wear

  • Astigmatism ≤1.00 D

  • Free of binocular vision disorder (strabismus, amblyopia, vergence dysfunction, accommodative dysfunction)

Exclusion Criteria:
  • No prior or concurrent participation in myopia control or use of low dose atropine, multifocal contact lenses

  • No use of any medications suspected to affect accommodation

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Ohio State University Columbus Ohio United States 43210

Sponsors and Collaborators

  • Ohio State University

Investigators

  • Principal Investigator: Ann M Morrison, OD, PhD, Ohio State University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ann Morrison, Assistant Professor, Ohio State University
ClinicalTrials.gov Identifier:
NCT06064617
Other Study ID Numbers:
  • 2023H0080
First Posted:
Oct 3, 2023
Last Update Posted:
Oct 3, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
Yes

Study Results

No Results Posted as of Oct 3, 2023