Office Based Vergence and Accommodative Therapy and Intermittent Exotropia

Pilot Study of Office Based Vergence and Accommodative Therapy as Treatment of Intermittent Exotropia

This pilot study is designed specifically to determine the short-term effect of OBVAT on intermittent exotropia in terms of 4 key areas (Standardizing reported outcomes of surgery for intermittent exotropia): control score, alignment, near stereoacuity and quality of life score. Result of this pilot study will be used to determine whether a full-scale RCT should be conducted to evaluate the short and long term effectiveness of OBVAT.

Study Overview

• Status: Unknown
• Conditions: Intermittent Exotropia
• Intervention / Treatment: Behavioral: accommodative/vergence therapy

Detailed Description

All enrolled px received 16-20 sessions of OBVAT, 60 minutes per visit, one time per week; Home reinforcement, 15 minutes each time, five times per week.

1. Primary outcome measure： A. Change in the office based intermittent exotropia control score
2. Secondary outcome measures A. Change in Look And Cover, then Ten seconds of Observation Scale for Exotropia (LACTOSE) B. Change in Newcastle Control Score (NCS) C. Change in Chinese intermittent exotropia questionnaire (CIXTQ) D. Change in near stereopsis by Preschool randot near stereoacuity E. Change in size of distant deviation angle by prism alternating cover test F. Change in size of near deviation angle by prism alternating cover test

• Study Type: Interventional
• Enrollment (Anticipated): 20
• Phase: Not Applicable

Contacts and Locations

Study Locations

• China
  • Guangdong
    • Guangzhou, Guangdong, China, 510000
      • Zhongshan Ophthalmic Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 8 years to 18 years (Child, Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. 8 to 18 years old
2. deviation meeting all of the following criteria: A. intermittent or constant exotropia at distance (mean of 3 baseline assessments of distance control> or = Grade 2) B. intermittent exotropia at near (at least 1 of 3 assessments of near control at the baseline visit Grade 2-4) C. distance and near exodeviation both between 15 to 35 prism diopters (PD) measured by prism and alternate cover test (PACT); D. near deviation not exceeding the distance deviation by >10PD by PACT (i.e., convergence insufficiency type IXT excluded)
3. cycloplegic objective refraction spherical equivalent (SE) refractive error between -6.00 diopters (D)and +1.00 D inclusive in either eye

4. Patients must be wearing the updated refractive correction (spectacles or contact lenses) for at least 1 week if refractive error (based on cycloplegic refraction performed within 6 months) meets any of the following:

   A. Myopia >-0.50 D spherical equivalent in either eye B. Anisometropia >1.00 D spherical equivalent C. Astigmatism in either eye >1.50 D

5. Refractive correction must meet the following guidelines:

   A. Anisometropia spherical equivalent must be within 0.25 D of the full anisometropic difference B. Astigmatism cylinder must be within 0.25 D of full correction and axis must be within 5 degree C. For hyperopia and myopia, the spherical component can be reduced by investigator discretion provided reduction is symmetrical and results in residual (i.e., uncorrected) spherical equivalent refractive error that does not exceed +1.50 D spherical equivalent hyperopia or -0.50 D spherical equivalent myopia

6. Gestational age >34 weeks
7. Birth weight >1500 g
8. No previous surgical or nonsurgical treatment for IXT other than single vision refractive correction (e.g. PALs, Bifocals, patching, or deliberate over-minus with spectacles more than 0.50 D)
9. No vision therapy or orthoptics for any reason within the last year
10. No prior strabismus surgery or botulinum injection, intraocular surgery, or refractive surgery
11. No strabismus surgery planned
12. vision correctable to at least 20/25 or better at distance and near in each eye.
13. Px needs to have a computer at home which can connect to internet

Exclusion Criteria:

1. Patient with nystagmus, restrictive or paretic strabismus
2. Patient with amblyopia, which is defined as >or = 0.2 logarithm of the minimum angle of resolution units of interocular difference and > or = 0.3 logarithm of the minimum angle of resolution units in one eye ( Variability of stereoacuity in intermittent exotropia)
3. Regular use of any ocular or systemic medications known to affect accommodation or vergence system, such as atropine, pirenzepine, and anti-epileptic medications in recent 3 months；
4. developmental disability, attention deficit hyperactivity disorder(ADHD), or learning disability diagnosis in children that in the investigator's discretion would interfere with office-based treatment；
5. Relocation anticipated for 2 years；
6. Significant ocular or neurologic disorders (e.g. cerebral palsy) other than strabismus
7. Vertical deviation greater than 1 pd in cover test
8. Household member already in the study.
9. Any eye care professional, ophthalmic technician, medical student, or optometry student

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Accommodative/vergence therapy; Accommodative/vergence therapy (60 minutes per visit, one time per week, 12-14 weeks) and home reinforcement (15 minutes each time, five times per week, 12-14 weeks) will be provided to patients of treatment group. These therapy includes accommodative, vergence and anti-suppression technique. No drug is used during the whole therapy process.	Behavioral: accommodative/vergence therapy; Accommodative/vergence therapy (60 minutes per visit, one time per week, 12-14 weeks) and home reinforcement (15 minutes each time, five times per week, 12-14 weeks) will be provided to patients of treatment group. These therapy includes accommodative, vergence and anti-suppression technique. No drug is used during the whole therapy process.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Office based intermittent exotropia control score	Office based intermittent exotropia control score is an office based score to assess the control of intermittent exotropia. Minimum score is 0 (best score, phoria) and Maximum score is 5(worst score, constant tropia). Change in Office based intermittent exotropia control score after 14 weeks of vision therapy	Baseline visit, 7th visit(7 weeks after BL), 15th visit (15 weeks after BL)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Look And Cover, then Ten seconds of Observation Scale for Exotropia(LACTOSE)	Look And Cover, then Ten seconds of Observation Scale for Exotropia (LACTOSE) is an office based score to assess the control of intermittent exotropia. Minimum score is 0 (best score, phoria) and Maximum score is 4(worst score, constant tropia). Change in score after 14 weeks of vision therapy.	Baseline visit, 7th visit(7 weeks after BL), 15th visit (15 weeks after BL)
Newcastle Control Score	Newcastle Control Score is an office based and home based score to assess the control of intermittent exotropia. Minimum score is 0 (best score) and Maximum score is 6(worst score). Change in score after 14 weeks of vision therapy.Change in score after 14 weeks of vision therapy.	Baseline visit, 7th visit(7 weeks after BL), 15th visit (15 weeks after BL)
Chinese intermittent exotropia questionnaire	Change in Chinese intermittent exotropia questionnaire after 14 weeks of vision therapy.	Baseline visit, 7th visit(7 weeks after BL), 15th visit (15 weeks after BL)
Preschool randot near stereoacuity	Change in near stereopsis by Preschool randot near stereoacuity after 14 weeks of vision therapy.	Baseline visit, 7th visit(7 weeks after BL), 15th visit (15 weeks after BL)
deviation angle	Change in size of distant deviation angle by prism alternating cover test after 14 weeks of vision therapy.	Baseline visit, 7th visit(7 weeks after BL), 15th visit (15 weeks after BL)

Collaborators and Investigators

• Sponsor: Sun Yat-sen University
• Investigators: Study Director: Chen xiang, associate chief physician

Publications and helpful links

General Publications

• Ma MM, Kang Y, Scheiman M, Chen X. Office-based Vergence and Accommodative Therapy for the Treatment of Intermittent Exotropia: A Pilot Study. Optom Vis Sci. 2019 Dec;96(12):925-933. doi: 10.1097/OPX.0000000000001454.

Study record dates

Study Major Dates

• Study Start (Actual): November 1, 2017
• Primary Completion (Actual): January 31, 2018
• Study Completion (Anticipated): December 30, 2018

Study Registration Dates

• First Submitted: October 15, 2017
• First Submitted That Met QC Criteria: October 23, 2017
• First Posted (Actual): October 26, 2017

Study Record Updates

• Last Update Posted (Actual): June 28, 2018
• Last Update Submitted That Met QC Criteria: June 26, 2018
• Last Verified: June 1, 2018

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Nervous System Diseases; Eye Diseases; Cranial Nerve Diseases; Ocular Motility Disorders; Strabismus; Exotropia
• Other Study ID Numbers: XT1

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Undecided

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No