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Clinical Trials/NCT00510562
NCT00510562CompletedNot Applicable

Effect of Cranial Osteopathy on Visual Function

Nova Southeastern University1 site in 1 country29 target enrollmentStarted: October 1, 2001Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
29
Locations
1
Primary Endpoint
Accommodative system testing Visual acuity testing Stereoacuity testing Vergence system testing Pupillary testing

Study Overview

Brief Summary

It is the purpose of this study to attempt to determine if there is an immediate, measurable change in visual function as a direct result following a session of cranial osteopathic manipulation.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Free of active ocular or systemic disease
  • •Refractive error between six diopters of myopia and five diopters of hyperopia with regular astigmatism of any amount
  • •Normal best-corrected visual acuity at 20/40 or better
  • •Normal amplitude of accommodation
  • •Willing to undergo cranial osteopathic manipulation

Exclusion Criteria

  • •Pregnancy
  • •History of previous closed head trauma or brain injury
  • •Students from the Nova Southeastern University Colleges of Osteopathic Medicine and Optometry
  • •Prior cranial manipulative treatment/craniosacral therapy

Arms & Interventions

1

Experimental

Assessment for cranial strain patterns, followed by indirect osteopathic treatment of dysfunctions found on assessment, followed by reassessment.

Intervention: Cranial osteopathic manipulation (Procedure)

2

Sham Comparator

Assessment for cranial strain patterns, followed by laying on of hands, followed by reassessment.

Intervention: Sham/Placebo (Procedure)

Outcomes

Primary Outcomes

Accommodative system testing Visual acuity testing Stereoacuity testing Vergence system testing Pupillary testing

Time Frame: Immediately after intervention.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mark Sandhouse

Associate Professor & Chair, Department of OPP

Nova Southeastern University

Study Sites (1)

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