MyopiaNCT07840209
Comparison of Hand Eye Coordination and Sports Vision Performance in Dual-Focus Multifocal Contact Lenses and Habitual Contact Lenses
A study testing Multifocal Contact Lens in people with Myopia, run by Ohio State University at 1 site in United States.
Trial summary
The purpose of the study is to compare the hand-eye coordination and sports vision performance in participants while they are wearing their habitual contact lenses versus while wearing the dual-focus multifocal contact lenses. Read more about this study
- Who is it for?
- Ages 18 to 38 years
- Conditions the study is for
- Myopia
- What is being tested?
- Multifocal Contact Lens
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 siteUnited States
- Study dates
- Oct 2026to Dec 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 38 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Adult, aged 18 to 38 with baseball or softball playing experience (high school or higher in the last 10 years)
- Ability to give informed consent
- Good general health defined by medication use that has not changed within the last 30 days and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the Investigator
- Current myopic spherical soft contact lens wearer with a prescription equivalent to the multifocal lens powers available
- Visual acuity of 20/25 or better in each eye with current soft contact lenses
- Visual acuity of 20/25 or better in each eye in multifocal contact lenses
Show all 10Show fewer
- Stereoacuity of 40" or better at 40 cm
- Willing to spend time required for attending 3 study visits and wearing contact lenses on days between study visits
- Any gender
- Any racial or ethnic origin
Who cannot join
- Current or active inflammation, infection, or eye disease as determined by the Investigator
- A systemic condition that in the opinion of the investigator may affect a study outcome
- Strabismus
- Unable to successfully wear the MiSight contact lenses for the duration of the study
- Females who are pregnant, lactating, or planning to conceive during the study
- Use of systemic or topical medication that in the opinion of the investigator may affect a study outcome variable
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site, 1 recruiting
- Recruiting
College of Optometry
Columbus, Ohio, 43210
iVERG Research Group, 614-292-8858, OPT-EyeStudies@osu.edu
About this study
The purpose of the study is to compare the hand-eye coordination and sports vision performance in participants while they are wearing their habitual contact lenses versus while wearing the dual-focus multifocal contact lenses.
- Conditions
- Myopia
- Being tested
- Multifocal Contact Lens
- Keywords
- Sports vision, contact lenses
- Medical subject headings
- Myopia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Multifocal Contact LensDevice
Multifocal Contact Lens
| Study group | Role | What they receive |
|---|---|---|
| Habitual contact lenses worn first, multifocal lenses worn second | Experimental | Participants will wear their habitual contact lenses while completing tasks first, then wear the provided multifocal lenses while completing tasks again. Receives: Device: Multifocal Contact Lens |
| Multifocal lenses worn first, habitual lenses worn second. | Experimental | Participants will wear the multifocal lenses while completing tasks first, then wear their habitual lenses while completing tasks again. Receives: Device: Multifocal Contact Lens |
What is being measured
The primary outcome is the main question the study is designed to answer.
Hand-eye coordination and sport vision performance
The average score of the AcuVision while wearing the multifocal contact lenses compared to the score when wearing their habitual contact lenses.
Measured: 3 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Sep 2026
- Study startOct 2026 (estimated)
- Primary completionDec 2027 (estimated)
- Study completionDec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for MyopiaStudies of the same condition, open and under way.
- More trials run by Ohio State UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Ohio State University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Jennifer Fogt, Ohio State University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07840209
- Sponsor's protocol ID
- STUDY20261434
- Status last verified
- Sep 2026
- First submitted
- 16 Sep 2026
- Last updated
- 24 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison of Hand Eye Coordination and Sports Vision Performance in Dual-Focus Multifocal Contact Lenses and Habitual Contact Lenses
- ClinicalTrials.gov ID
- NCT07840209
- Acronym / sponsor ID
- STUDY20261434
- Conditions
- Myopia
- Keywords
- Sports vision, contact lenses
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- Ohio State UniversityUniversity, hospital or other
- Study start
- Oct 2026 (estimated)
- Primary completion
- Dec 2027 (estimated)
- Study completion
- Dec 2027 (estimated)
- First posted
- 24 Sep 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of the study is to compare the hand-eye coordination and sports vision performance in participants while they are wearing their habitual contact lenses versus while wearing the dual-focus multifocal contact lenses.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Habitual contact lenses worn first, multifocal lenses worn second | Experimental | Device: Multifocal Contact LensParticipants will wear their habitual contact lenses while completing tasks first, then wear the provided multifocal lenses while completing tasks again. |
| Multifocal lenses worn first, habitual lenses worn second. | Experimental | Device: Multifocal Contact LensParticipants will wear the multifocal lenses while completing tasks first, then wear their habitual lenses while completing tasks again. |
Who may qualify
- Ages
- 18 to 38 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (10 listed)
- Adult, aged 18 to 38 with baseball or softball playing experience (high school or higher in the last 10 years)
- Ability to give informed consent
- Good general health defined by medication use that has not changed within the last 30 days and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the Investigator
- Current myopic spherical soft contact lens wearer with a prescription equivalent to the multifocal lens powers available
- Visual acuity of 20/25 or better in each eye with current soft contact lenses
Key exclusion criteria (6 listed)
- Current or active inflammation, infection, or eye disease as determined by the Investigator
- A systemic condition that in the opinion of the investigator may affect a study outcome
- Strabismus
- Unable to successfully wear the MiSight contact lenses for the duration of the study
- Females who are pregnant, lactating, or planning to conceive during the study
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Multifocal Contact LensMultifocal Contact Lens | Device | Habitual contact lenses worn first, multifocal lenses worn second, Multifocal lenses worn first, habitual lenses worn second. |
Primary outcome
Hand-eye coordination and sport vision performance
Time frame: 3 weeks
The average score of the AcuVision while wearing the multifocal contact lenses compared to the score when wearing their habitual contact lenses.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Sep 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Multifocal Contact Lens in people with Myopia, run by Ohio State University at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 10 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 24 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact iVERG Reserch Group (614-292-8858, OPT-EyeStudies@osu.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Hand-eye coordination and sport vision performance (time frame: 3 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Sep 2026.