PPCS-CI: Persistent Post-Concussion Symptoms With Convergence Insufficiency

Sponsor

New Jersey Institute of Technology (Other)

Overall Status

Recruiting

CT.gov ID

NCT05262361

Collaborator

Salus University (Other), Children's Hospital of Philadelphia (Other), Somerset Pediatric Group (Other), National Eye Institute (NEI) (NIH), Rutgers University (Other)

100

Enrollment

Locations

Arms

59.9

Anticipated Duration (Months)

33.3

Patients Per Site

0.6

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Our successful R01 discovered 1) the neural mechanistic difference between typically occurring convergence insufficiency (TYP-CI) and binocularly normal controls and 2) the underlying mechanism of office-based vergence and accommodative therapy (OBVAT) that is effective in remediating symptoms. Adolescent and young adult concussion is considered a substantial health problem in the United States where our team has shown that about half of patients with persistent post-concussion symptoms have convergence insufficiency (PPCS-CI), causing significant negative impact associated with reading or digital screen-related activities, and is believed to be one factor causing delayed recovery impacting return to school, sports, or work. The results of this randomized clinical trial will impact the lives of adolescents and young adults with PPCS-CI to guide professionals on how to manage and treat those with PPCS-CI by 1) comparing the differences between PPCS-CI and TYP-CI, 2) discovering the neural mechanism of OBVAT for PPCS-CI compared to standard-community concussion care, and 3) determining the effectiveness of 12 one-hour sessions compared to 16 one-hour sessions of OBVAT.

Condition or Disease	Intervention/Treatment	Phase
Persistent Post-concussive Symptoms Convergence Insufficiency Mild Traumatic Brain Injury Concussion, Mild Concussion; Eye	Behavioral: Office-based Vergence and Accommodative Therapy	N/A

Detailed Description

During the past 6 years, our study team investigated the neural mechanism of typically-occurring convergence insufficiency (TYP-CI), the most common binocular vision disorder in children and young adults (3.4% to 12.7%5-11). We conducted the only randomized clinical trial (RCT) integrating objective eye movement and fMRI outcome measures, achieving 100% planned enrollment and retention of 100 young adults. Our results localized the reduction in functional activity for TYP-CI compared to controls within the oculomotor vermis (OVM) and the cuneus. Functional activity in the OVM and cuneus was significantly correlated to convergence peak velocity providing the first mechanistic identification of these deficits that create significant burden to those afflicted. Our longitudinal results discovered that the neural mechanistic change stimulated by office-based vergence /accommodative therapy (OBVAT) is an increase in the frontal eye field (FEF) and thalamus functional activity. Increased functional activity from the FEF and thalamus significantly correlates to convergence peak velocity. Results are leading to personalized point-of-care therapies remediating the debilitating symptoms for TYP-CI patients. While our research and results of other RCTs show that OBVAT is the most effective treatment for remediating symptoms and improving vision function in both TYP-CI children and adults, none of these participants had a history of head injury, a pathology that has been linked to CI. Our research team has demonstrated that the prevalence of CI is higher (38% to 49%) in children and adults with persistent post-concussive symptoms (PPCS-CI), than in the non-concussed population. Currently, there is no validated treatment for PPCS-CI. This difference in prevalence, mode of onset (longstanding versus sudden onset), and severity of the condition has led to a debate about whether the diagnostic and management procedures effective for TYP-CI should be utilized for PPCS-CI, and strongly suggests that new research is needed to optimize PPCS-CI management. We are uniquely positioned to provide answers to these questions by building on our work establishing the neurofunctional mechanism of TYP-CI and OBVAT administered to TYP-CI. Such research is of great importance because PPCS-CI is associated with debilitating visual symptoms impacting the return to school/sports, work, or driving. We have identified three significant gaps for the treatment of PPCS-CI that must be addressed to determine its most effective management. First, given the obvious differences in etiology, are there significant differences between TYP-CI and PPCS-CI related to objective eye movement measures (peak velocity, final amplitude, and repeatability) due to underlying neural mechanistic differences? Second, what is the underlying neural mechanism of OBVAT for PPCS-CI compared to TYP-CI? Third, how effective is OBVAT for PPCS-CI and is the dosage of administration different than TYP-CI? This renewal addresses these gaps in clinical science.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

100 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Intervention Model Description:

The are two arms. Arm 1 will have participants will have office-based vergence and accommodative therapy (twice per week) immediately after enrollment while arm 2 will have participants have a 6 week delay before enrollment of therapy. There are three assessments: baseline, outcome 1 which is at 6 weeks (arm 1 would be after 12 sessions of therapy and arm 2 would not have participants in vision therapy yet), and outcome 2 which after vision therapy.The are two arms. Arm 1 will have participants will have office-based vergence and accommodative therapy (twice per week) immediately after enrollment while arm 2 will have participants have a 6 week delay before enrollment of therapy. There are three assessments: baseline, outcome 1 which is at 6 weeks (arm 1 would be after 12 sessions of therapy and arm 2 would not have participants in vision therapy yet), and outcome 2 which after vision therapy.

Masking:

Single (Outcomes Assessor)

Masking Description:

The optometrist will be masked for all outcome assessments.

Primary Purpose:

Treatment

Official Title:

Functional Mechanism of Neural Control in Persistent Post-Concussion Symptoms Convergence Insufficiency

Actual Study Start Date :

Sep 1, 2021

Anticipated Primary Completion Date :

Sep 1, 2025

Anticipated Study Completion Date :

Aug 28, 2026

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Office based Vergence and Accommodative Therapy immediately after enrollement This arm will start immediately after baseline assessment. The participant will have two sessions of one hour each for 6 weeks (12 office-based vergence and accommodative therapy sessions). The first outcome measurement will be attained by a masked optometrist. Then, the participant will have 2 more weeks of therapy (4 office-based vergence and accommodative therapy sessions). The second and final outcome measurement will be attained. Assessments include a masked optometric vision exam, objective eye movement recordings and an functional MRI scan.	Behavioral: Office-based Vergence and Accommodative Therapy Office-based Vergence and Accommodative Therapy has four phases which start with gross vergence and accommodation. Disparity vergence is isolated using instruments such as vectograms and accommodation is isolated using near far charts and accommodative rock. The final phase includes the integration of vergence and accommodation to increase range and visual comfort which performing activities close to the person.
No Intervention: Office based Vergence and Accommodative Therapy Delay 6 weeks post enrollment This arm will start with a 6 week delay (no vision therapy) after baseline assessment to evaluate natural recovery. After 6 weeks, the first outcome assessment will be attained by a masked optometrist. The participant will have two sessions of one hour each for 8 weeks (16 office-based vergence and accommodative therapy sessions). The second and final outcome measurement will be attained. Assessments include a masked optometric vision exam, objective eye movement recordings and an functional MRI scan.

Arm

Intervention/Treatment

Experimental: Office based Vergence and Accommodative Therapy immediately after enrollement

This arm will start immediately after baseline assessment. The participant will have two sessions of one hour each for 6 weeks (12 office-based vergence and accommodative therapy sessions). The first outcome measurement will be attained by a masked optometrist. Then, the participant will have 2 more weeks of therapy (4 office-based vergence and accommodative therapy sessions). The second and final outcome measurement will be attained. Assessments include a masked optometric vision exam, objective eye movement recordings and an functional MRI scan.

Behavioral: Office-based Vergence and Accommodative Therapy

Office-based Vergence and Accommodative Therapy has four phases which start with gross vergence and accommodation. Disparity vergence is isolated using instruments such as vectograms and accommodation is isolated using near far charts and accommodative rock. The final phase includes the integration of vergence and accommodation to increase range and visual comfort which performing activities close to the person.

No Intervention: Office based Vergence and Accommodative Therapy Delay 6 weeks post enrollment

This arm will start with a 6 week delay (no vision therapy) after baseline assessment to evaluate natural recovery. After 6 weeks, the first outcome assessment will be attained by a masked optometrist. The participant will have two sessions of one hour each for 8 weeks (16 office-based vergence and accommodative therapy sessions). The second and final outcome measurement will be attained. Assessments include a masked optometric vision exam, objective eye movement recordings and an functional MRI scan.

Outcome Measures

Primary Outcome Measures

Near Point of Convergence with Positive Fusional Vergence [after 12 therapy session spanning 6 weeks]
Composite score of how close a participant can view a target a single along midline combined with positive fusional vergence range.

Secondary Outcome Measures

Vergence Peak Velocity [after 12 therapy session spanning 6 weeks]
The maximum speed of a person looking from far to near along midline
Functional Activity within vergence neural circuit [after 12 therapy session spanning 6 weeks]
The amount of blood oxygenation level dependent signal from vergence neural circuit

Eligibility Criteria

Criteria

Ages Eligible for Study:

13 Years to 25 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Between 13 to 25 years
Concussion diagnosed by a clinical 1 to 3 months ago
Best-corrected visual acuity of 20/25 in both eyes at distance and near
willing to wear glasses or contact to correct refractive error if needed
Global stereopsis of 500 sec of arc or better and 70 sec of arc of better using Randot Stereo Test
Diagnosis of convergence insufficiency from an optometrist defined as near point of convergence of greater than or equal to 6 cm, positive fusional vergence at 40 cm not meeting Sheard's criteria of at least twice the near phoria or a range of less than or equal to 15 prism diopters, and a convergence insufficiency symptom survey score of 21 or greater for adults or 16 or greater for children.

Exclusion Criteria:

History of performing office or home-based vision therapy, orthoptics, home-based near target push-ups, or pencil push ups
Amblyopia (lazy eye) or constant strabismus or strabismus surgery
Any conditions or diseases that affect accommodation, vergence or ocular motility, such as Multiple Sclerosis, Graves' thyroid disease, Myastheria Gravis, Diabetes, Chemotherapy, or Parkinson's Disease
Non-removable metal in the body
Pregnant, planning on becoming pregnant during the study duration, or breastfeeding
Metal worker

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	NJIT	Newark	New Jersey	United States	07102
2	Somerset Pediatric Group	Raritan	New Jersey	United States	08869
3	The Children's Hospital of Philadelphia	Philadelphia	Pennsylvania	United States	19104

Sponsors and Collaborators

New Jersey Institute of Technology
Salus University
Children's Hospital of Philadelphia
Somerset Pediatric Group
National Eye Institute (NEI)
Rutgers University

Investigators

Principal Investigator: Tara L Alvarez, PhD, New Jersey Institute of Technology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Dr. Tara Lynn Alvarez, Professor, New Jersey Institute of Technology

ClinicalTrials.gov Identifier:

NCT05262361

Other Study ID Numbers:

2R01EY023261
2R01EY023261

First Posted:

Mar 2, 2022

Last Update Posted:

Mar 2, 2022

Last Verified:

Feb 1, 2022

Individual Participant Data (IPD) Sharing Statement:

Yes

Plan to Share IPD:

Yes

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Additional relevant MeSH terms:

Brain Injuries

Brain Injuries, Traumatic

Brain Concussion

Ocular Motility Disorders

Post-Concussion Syndrome

Study Results

No Results Posted as of Mar 2, 2022