Overview

Effects of Stulln and Accommodative Training

Status:
Withdrawn
Trial end date:
2021-08-31
Target enrollment:
0
Participant gender:
All
Summary
The present study tests the hypothesis that Stulln eyedrops improve accommodative functions by improving the short term facility of ciliary muscles that can be transferred into long-term adaptation. To test this, the investigators propose to conduct a prospective randomized control trials where participants with accommodative dysfunctions are randomly assigned to four groups: control, Stulln only and Stulln plus vision training. The investigators' theory predicts that the efficacy of Stulln will be augmented by vision training.
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Pacific University
Treatments:
Ophthalmic Solutions
Criteria
Inclusion Criteria:

- Be between 18 and 45 years of age.

- Have normal/corrected-to-normal monocular acuity of better than 20/25 for both eyes.

- Have normal contrast sensitivity.

- Be a native English speakers or possess college-level English reading proficiency.

- Have a current optical prescription (obtained less than 2 years ago).

- Have accommodative dysfunctions, including reduced accommodative amplitude, range,
facility and endurance.

Exclusion Criteria:

- Have no prismatic correction.

- No clinically significant ocular pathology (e.g., cataract, keratoconus, dry eye,
diabetic retinopathy, or age-related macular degeneration) that would limit the
effectiveness of vision training.

- Have no binocular dysfunction, including amblyopia, strabismus, and other binocular
diseases that would impede accommodative training.