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Randomized Trial of Treatments for Convergence Insufficiency

Primary Purpose

Convergence Insufficiency

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Pencil Push-ups
Office-based Vision Therapy
Placebo Office-based Vision Therapy
Sponsored by
Pennsylvania College of Optometry
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Convergence Insufficiency focused on measuring convergence insufficiency, vision therapy, orthoptics

Eligibility Criteria

9 Years - 30 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Age 9-30 years Best corrected visual acuity of 20/25 in both eyes at distance and near Willingness to wear eyeglasses or contact lenses to correct refractive error, if necessary Exophoria at near at least 4 prism diopters greater than at far Insufficient positive fusional convergence (i.e., failing Sheard's criterion or minimum normative positive fusional vergence (PFV) of 15 base-out break). Receded near point of convergence of > 6 cm break. Normal random dot stereopsis using a 500 seconds of arc target. CI Symptom Survey score > 16 for subjects in 9-18 year age range and > 21 for subjects in the 19-30 year age range. Informed consent and willingness to participate in the study and be randomized Exclusion Criteria: CI previously treated with pencil push-ups (no more than 2 months of treatment within the past year) CI previously treated with office-based vision therapy/orthoptics (no more than 2 months of treatment within the past year) Amblyopia Constant strabismus History of strabismus surgery Anisometropia >1.50D difference between eyes Prior refractive surgery Vertical heterophoria greater than 1  Systemic diseases known to affect accommodation, vergence, and ocular motility such as: multiple sclerosis, Graves's thyroid disease, myasthenia gravis, diabetes, and Parkinson disease Any ocular or systemic medication known to affect accommodation or vergence Monocular accommodative amplitude less than 4 D in either eye as measured by the Donder's push-up method Manifest or latent nystagmus Attention deficit hyperactivity disorder (ADHD) or learning disability diagnosis by parental report Household member or sibling already enrolled in the CITT Any eye care professional, technician, medical student, or optometry student

Sites / Locations

  • Southern California College of Optometry
  • State University of New York, College of Optometry
  • The Ohio State University, Optometry Coordinating Center
  • The Ohio State University
  • Pacific University College of Optometry
  • Eye Institute, Pennsylvania College of Optometry
  • University of Houston, College of Optometry

Outcomes

Primary Outcome Measures

The primary outcome measure is the score on the Convergence Insufficiency Symptom Survey

Secondary Outcome Measures

Near Point of Convergence
Positive Fusional Vergence at Near

Full Information

First Posted
July 3, 2006
Last Updated
July 3, 2006
Sponsor
Pennsylvania College of Optometry
Collaborators
National Eye Institute (NEI)
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1. Study Identification

Unique Protocol Identification Number
NCT00347945
Brief Title
Randomized Trial of Treatments for Convergence Insufficiency
Official Title
A Randomized Clinical Trial of Pencil Push-Ups Versus Office Based Vision Therapy For the Treatment of Convergence Insufficiency
Study Type
Interventional

2. Study Status

Record Verification Date
January 2002
Overall Recruitment Status
Completed
Study Start Date
October 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
November 2001 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Pennsylvania College of Optometry
Collaborators
National Eye Institute (NEI)

4. Oversight

5. Study Description

Brief Summary
The Convergence Insufficiency Treatment Trial (CITT) is a multi-center, placebo-controlled, single-masked, clinical trial designed to compare the benefits of two commonly used treatment approaches for patients with convergence insufficiency (CI)
Detailed Description
Considerable controversy exists regarding the best treatment for convergence insufficiency (CI), a common condition that often interferes with the ability to perform near work. The two most widely used treatments have significant differences in costs and in practitioner perceived utility. Pencil push-up therapy (PPT) is a simple, low-cost treatment in which patients are prescribed a single procedure to perform at home with only periodic follow-up. Office-based vision therapy (OBVT) is a more comprehensive, time-consuming, complex, and costly treatment in which patients are scheduled for weekly in-office therapy visits and are often prescribed a specific sequence of therapeutic procedures to perform at home. It is important to consider whether either, neither, or both treatments are effective. The Convergence Insufficiency Treatment Trial (CITT) is a prospective, masked-examiner, multi-center clinical trial in which patients are randomized to one of these two treatment approaches. The primary goal is to answer the following question: After 12 weeks of treatment, is one therapy more effective than the other in improving CI signs and symptoms? We will test the null hypothesis that there is no difference in the distribution of outcomes between the two populations. The primary outcome measure will be a classification of each patient as a "success," "improvement," or "failure." This classification will be based on the level of improvement in both the signs (near point of convergence and positive fusional vergence) and symptoms of CI. Additional questions relate to longer term effects: Are the patients who were classified as "success" or "improvement" at twelve weeks the same at the one-year follow-up for each treatment group? Are there differences in the distributions of changes in near point of convergence, positive fusional vergence, or accommodative amplitudes, between the two treatment groups, at twelve weeks and at one-year of follow up?

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Convergence Insufficiency
Keywords
convergence insufficiency, vision therapy, orthoptics

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
Single
Allocation
Randomized
Enrollment
90 (false)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Pencil Push-ups
Intervention Type
Procedure
Intervention Name(s)
Office-based Vision Therapy
Intervention Type
Procedure
Intervention Name(s)
Placebo Office-based Vision Therapy
Primary Outcome Measure Information:
Title
The primary outcome measure is the score on the Convergence Insufficiency Symptom Survey
Secondary Outcome Measure Information:
Title
Near Point of Convergence
Title
Positive Fusional Vergence at Near

10. Eligibility

Sex
All
Minimum Age & Unit of Time
9 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 9-30 years Best corrected visual acuity of 20/25 in both eyes at distance and near Willingness to wear eyeglasses or contact lenses to correct refractive error, if necessary Exophoria at near at least 4 prism diopters greater than at far Insufficient positive fusional convergence (i.e., failing Sheard's criterion or minimum normative positive fusional vergence (PFV) of 15 base-out break). Receded near point of convergence of > 6 cm break. Normal random dot stereopsis using a 500 seconds of arc target. CI Symptom Survey score > 16 for subjects in 9-18 year age range and > 21 for subjects in the 19-30 year age range. Informed consent and willingness to participate in the study and be randomized Exclusion Criteria: CI previously treated with pencil push-ups (no more than 2 months of treatment within the past year) CI previously treated with office-based vision therapy/orthoptics (no more than 2 months of treatment within the past year) Amblyopia Constant strabismus History of strabismus surgery Anisometropia >1.50D difference between eyes Prior refractive surgery Vertical heterophoria greater than 1  Systemic diseases known to affect accommodation, vergence, and ocular motility such as: multiple sclerosis, Graves's thyroid disease, myasthenia gravis, diabetes, and Parkinson disease Any ocular or systemic medication known to affect accommodation or vergence Monocular accommodative amplitude less than 4 D in either eye as measured by the Donder's push-up method Manifest or latent nystagmus Attention deficit hyperactivity disorder (ADHD) or learning disability diagnosis by parental report Household member or sibling already enrolled in the CITT Any eye care professional, technician, medical student, or optometry student
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mitchell Scheiman, OD
Organizational Affiliation
Pennsylvania College of Optometry
Official's Role
Study Chair
Facility Information:
Facility Name
Southern California College of Optometry
City
Fullerton
State/Province
California
ZIP/Postal Code
92831
Country
United States
Facility Name
State University of New York, College of Optometry
City
New York
State/Province
New York
ZIP/Postal Code
10036
Country
United States
Facility Name
The Ohio State University, Optometry Coordinating Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Facility Name
The Ohio State University
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Facility Name
Pacific University College of Optometry
City
Forest Grove
State/Province
Oregon
ZIP/Postal Code
97116
Country
United States
Facility Name
Eye Institute, Pennsylvania College of Optometry
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19141
Country
United States
Facility Name
University of Houston, College of Optometry
City
Houston
State/Province
Texas
ZIP/Postal Code
77204
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
14688547
Citation
Borsting EJ, Rouse MW, Mitchell GL, Scheiman M, Cotter SA, Cooper J, Kulp MT, London R; Convergence Insufficiency Treatment Trial Group. Validity and reliability of the revised convergence insufficiency symptom survey in children aged 9 to 18 years. Optom Vis Sci. 2003 Dec;80(12):832-8. doi: 10.1097/00006324-200312000-00014.
Results Reference
background
PubMed Identifier
11999152
Citation
Gallaway M, Scheiman M, Malhotra K. The effectiveness of pencil pushups treatment for convergence insufficiency: a pilot study. Optom Vis Sci. 2002 Apr;79(4):265-7. doi: 10.1097/00006324-200204000-00013.
Results Reference
background
PubMed Identifier
11913841
Citation
Scheiman M, Cooper J, Mitchell GL, de LP, Cotter S, Borsting E, London R, Rouse M. A survey of treatment modalities for convergence insufficiency. Optom Vis Sci. 2002 Mar;79(3):151-7. doi: 10.1097/00006324-200203000-00009.
Results Reference
background
PubMed Identifier
15642806
Citation
Scheiman M, Mitchell GL, Cotter S, Cooper J, Kulp M, Rouse M, Borsting E, London R, Wensveen J; Convergence Insufficiency Treatment Trial Study Group. A randomized clinical trial of treatments for convergence insufficiency in children. Arch Ophthalmol. 2005 Jan;123(1):14-24. doi: 10.1001/archopht.123.1.14.
Results Reference
result
PubMed Identifier
16044063
Citation
Scheiman M, Mitchell GL, Cotter S, Kulp MT, Cooper J, Rouse M, Borsting E, London R, Wensveen J. A randomized clinical trial of vision therapy/orthoptics versus pencil pushups for the treatment of convergence insufficiency in young adults. Optom Vis Sci. 2005 Jul;82(7):583-95. doi: 10.1097/01.opx.0000171331.36871.2f.
Results Reference
result
PubMed Identifier
33263359
Citation
Scheiman M, Kulp MT, Cotter SA, Lawrenson JG, Wang L, Li T. Interventions for convergence insufficiency: a network meta-analysis. Cochrane Database Syst Rev. 2020 Dec 2;12(12):CD006768. doi: 10.1002/14651858.CD006768.pub3.
Results Reference
derived
Links:
URL
http://optometry.osu.edu/research/CITT/
Description
Study Website

Learn more about this trial

Randomized Trial of Treatments for Convergence Insufficiency

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