RECRUITING

Acuvue Oaysis Contact Lens Wearers Being Refit Into P7 Contact Lenses

Conditions

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Determine the likelihood of successfully refitting a satisfied AOA CL wearers into P7A CLs

Official Title

How Does PRECISION7® for Astigmatism Perform in Current and Successful Acuvue® Oasys for Astigmatism Wearers?

Quick Facts

Study Start:2025-04-15

Study Completion:2025-10-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06955403

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 40 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT

Inclusion Criteria	Exclusion Criteria
1. Adults, 18- to 40-year-old, AOA CL wearers with best-corrected 20/20 visual acuity or better. 2. Participants will be required to have worn AOA CLs for at least 3 months in the past year and currently wearing these CLs. 3. All participants will be required to have a CLDEQ-8 score \<12 while wearing their habitual CLs (AOA CLs) and to indicate that they are satisfied with AOA CLs (Yes/No). 4. Participants will be required to be able to wear P7A CLs (astigmatism ≥0.75D OD/OS). 5. Astigmatism ranging from 0.75 D to 2.50 D in each eye 6. Participants will be required to wear the study CLs for ≥13 hours with no overnight wear 7. Participants will be willing to wear the CL every day of the week, except during the washout period 8. Participants will be required to provide a glasses prescription that is less than 3 years old	* 1. Have presbyopia and/or need a reading add as determined during their initial manifest refraction 2. Have worn P7A in the past 3. Are past rigid CL wearers 4. Have a history of being diagnosed with dry eye or ocular allergies 5. Have known systemic health conditions that are thought to alter tear film physiology 6. Have a history of viral eye disease 7. Have a history of ocular surgery 8. Have a history of severe ocular trauma 9. Have a history of corneal dystrophies or degenerations 10. Have active ocular infection or inflammation 11. Are currently using isotretinoin-derivatives or ocular medications 12. Are pregnant or breast feeding

Inclusion Criteria

Exclusion Criteria

1. Adults, 18- to 40-year-old, AOA CL wearers with best-corrected 20/20 visual acuity or better.
2. Participants will be required to have worn AOA CLs for at least 3 months in the past year and currently wearing these CLs.
3. All participants will be required to have a CLDEQ-8 score \<12 while wearing their habitual CLs (AOA CLs) and to indicate that they are satisfied with AOA CLs (Yes/No).
4. Participants will be required to be able to wear P7A CLs (astigmatism ≥0.75D OD/OS).
5. Astigmatism ranging from 0.75 D to 2.50 D in each eye
6. Participants will be required to wear the study CLs for ≥13 hours with no overnight wear
7. Participants will be willing to wear the CL every day of the week, except during the washout period
8. Participants will be required to provide a glasses prescription that is less than 3 years old

* 1. Have presbyopia and/or need a reading add as determined during their initial manifest refraction 2. Have worn P7A in the past 3. Are past rigid CL wearers 4. Have a history of being diagnosed with dry eye or ocular allergies 5. Have known systemic health conditions that are thought to alter tear film physiology 6. Have a history of viral eye disease 7. Have a history of ocular surgery 8. Have a history of severe ocular trauma 9. Have a history of corneal dystrophies or degenerations 10. Have active ocular infection or inflammation 11. Are currently using isotretinoin-derivatives or ocular medications 12. Are pregnant or breast feeding

Contacts and Locations

Study Contact

Chris Lievens, OD

CONTACT

9014815699

clievens@sco.edu

Principal Investigator

Chris Lievens

PRINCIPAL_INVESTIGATOR

The Southern College of Optometry

Study Locations (Sites)

The Southern College of Optometry

Memphis, Tennessee, 38104

United States

Collaborators and Investigators

Sponsor: Southern College of Optometry

Chris Lievens, PRINCIPAL_INVESTIGATOR, The Southern College of Optometry

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-04-15

Study Completion Date2025-10-30

Study Record Updates

Study Start Date2025-04-15

Study Completion Date2025-10-30

Terms related to this study

Additional Relevant MeSH Terms

Contact Lens Comfort