- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05018390
Impact of Osteopathic Manipulative Treatment on Pursuit Eye Movements in Healthy Human Adults
Impact of Osteopathic Manipulative Treatment on External Lateral Ocular Pursuit, Measured in Healthy Human Adults: a Randomized, Double-blind, Controlled Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Our hypothesis is based on the implication of the fascial system (i.e., connective tissues) in the structural continuity that gives form and function to every tissue and organ. Fascial tissue, on which osteopathic manipulations are acting by restoring its elasticity, is also present in the eye cavity. The connection between fascia might explain how osteopathic manipulations, applied on structures which can be far from the original dysfunctional point, might improve oculomotricity.
Before and after OMT, practitioners will estimate the lateral and medial oculomotor muscles' and the fascia's tissue elasticity with a manual test. They will softly mobilize the eyeballs in medial and lateral directions (the amplitude of these passive mobilizations will always be lower than active eye rotations) and give an elasticity score. Before and after these tests, pursuit eye movements will be recorded by an independent technician. Participants will be asked to track a target that will be displaced horizontally on a computer screen. The target will move 30 times from left to right and 30 times from right to left with a constant speed of 20 degrees of visual angle per second.
The study will involve three independent groups (experimental, sham, test-retest) of healthy participants. We expect that pursuit improvement will be larger in the experimental group than in the two other groups. Moreover, as secondary goals, we will evaluate the correlation between pursuit eye movement data (obtained with a technical device, in a standardized situation) and subjective assessments of oculomotor muscles' elasticity made by the practitioners providing OMTs. We will also examine the possible practitioner effect (two exclusive osteopaths will provide OMTs).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Paris, France, 75015
- Ecole d'Osteopathie de Paris
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adult between 18 and 35 years of age
- Affiliated to the French Social Security scheme
- Ability to understand and sign the written consent form
Exclusion Criteria:
- Eye movements that cannot be calibrated correctly and therefore measured by the eye-tracker
- Visual deficit that prevents from performing the ocular task
- Pregnancy or breastfeeding
- Neurologic, psychiatric or epileptic disorder, or any other neuromuscular disorder
- Medical treatment affecting the central, autonomous or peripheral nervous system, or affecting vigilance and/or attention
- Skull fracture less than 12 months ago, symptomatic whiplash less than 3 months ago, spinal pain, fever, abdominal or pelvic pain, myopathy, ocular pain, or nystagmus
- Legal protection
- Major risk to develop severe corona virus disease illness, or living with people presenting such a risk
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: OMT
Osteopathic manipulative treatment : participants will receive low-amplitude tissue mobilizations on peripheral, vertebral, cranial and/or visceral articular systems.
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Participants will be positioned on an exam table supine, seated, or decubitus.
Osteopathic manipulations will consist in corrective micro-movements applied on synovial joints, on the skull, the teeth and/or visceral structures of the abdomen or the thorax.
Local pressures won't exceed a few tens of grams/cm².
Practitioners will realize between 15 and 25 technical gestures per participant.
Treatment will last 30 minutes (plus or minus 5 minutes) on average.
The technical gestures are referenced in the Glossary of Osteopathic Terminology published by the American Association of Colleges of Osteopathic Medicine (2017).
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Sham Comparator: Sham
Participants will be applied gestures that look like actual osteopathic manipulations but are not therapeutic.
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Participants will be positioned on an exam table supine, seated, or decubitus.
They will receive 20 gestures that will be standardized and different from actual osteopathic manipulations (but not identifiable as sham manipulations by the participants).
The duration of the sham treatment will be the same as the actual treatment.
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No Intervention: Test-retest
Participants will undergo the two eye movement measurements, but will not receive any (actual or sham) treatment.
30 minutes will elapse between the two measurements.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Duration of external lateral ocular pursuit
Time Frame: immediately before treatment
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Time spent to track a moving target, by generating smooth eye movements (as opposed to ocular saccades) with a velocity close to the target velocity.
Metric: millisecond.
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immediately before treatment
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Mean change from baseline in duration of external lateral ocular pursuit
Time Frame: immediately after treatment
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Change from baseline in time spent to track a moving target, by generating smooth eye movements (as opposed to ocular saccades) with a velocity close to the target velocity.
Metric: millisecond.
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immediately after treatment
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Reaction time
Time Frame: immediately before treatment
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Time elapsed between target displacement initiation and ocular pursuit initiation.
Metric: millisecond.
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immediately before treatment
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Mean change from baseline in reaction time
Time Frame: immediately after treatment
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Mean change from baseline in time elapsed between target displacement initiation and ocular pursuit initiation.
Metric: millisecond.
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immediately after treatment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Score on the test of eyeball passive manual mobilization
Time Frame: immediately before treatment
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Tissue elasticity of an oculomotor muscle will be assessed using a 3-points scale (1 = no resistance to the mobilization, 3 = strong resistance).
Four muscles (two per eyeball) will be assessed.
Maximal score = 12 points.
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immediately before treatment
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Score on the test of eyeball passive manual mobilization
Time Frame: immediately after treatment
|
Tissue elasticity of an oculomotor muscle will be assessed using a 3-points scale (1 = no resistance to the mobilization, 3 = strong resistance).
Four muscles (two per eyeball) will be assessed.
Maximal score = 12 points.
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immediately after treatment
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Mohamed Gharmaoui, MD, Ecole d'Osteopathie de Paris
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- OSTEOM-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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