The purpose of this study is to determine if there is a measurable change in visual function as a direct result of the application of osteopathic cranial manipulative medicine. The study will also attempt to determine whether any changes noted remain after withdrawal of the treatment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
113
Performed by exaggerating the motion asymmetry with a minimum of pressure (a few ounces) and holding the position until the motion becomes symmetrical.
A laying on of hands with no actual treatment being performed.
Nova Southeastern University Davie Health Center
Fort Lauderdale, Florida, United States
Distance Visual Acuity
Measurement of visual acuity in each eye by number of letters read correctly on ETDRS chart.
Time frame: Weekly for 16 weeks
Accommodative System Testing
Accommodative amplitude testing using a Donder push-up card.
Time frame: Weekly for 16 weeks
Local Stereoacuity Testing
Measured by Random Dot E test.
Time frame: Weekly for 16 weeks
Pupillary Size Testing
Measurement of pupil size (each eye) in bright and dim light.
Time frame: Weekly for 16 weeks
Vergence System Testing
Assessed by Cover Test with Prism Neutralization and Near Point of Convergence
Time frame: Weekly for 16 weeks
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