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Bilateral Transcranial Direct Current Stimulation and Ocular Occlusion for Adults With Amblyopia

Primary Purpose

Amblyopia

Status
Terminated
Phase
Not Applicable
Locations
Chile
Study Type
Interventional
Intervention
Bilateral transcranial direct current stimulation
Sponsored by
University of Chile
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Amblyopia focused on measuring Lazy eye syndrome, Transcranial direct current stimulation, Ocular occlusion, Amblyopia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Prior diagnosis of Amblyopia

Exclusion Criteria:

  • Ophthalmologic disease other than amblyopia
  • Chronic pharmacological therapy
  • Implanted medical device
  • Neurologic disease or surgery history
  • History of an adverse reaction to tDCS
  • Pregnancy
  • Not able to give informed consent

Sites / Locations

  • Faculty of Medicine of University of Chile

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

Sham bilateral transcranial direct current stimulation

Bilateral transcranial direct current stimulation

Arm Description

Sham bilateral transcranial direct current stimulation consisted of 2 milliamperes (mA) of current from the anodal electrode in the amblyopic primary visual cortex to the cathodal electrode located in the fellow primary visual cortex, but the stimulation was turned off after 30 seconds. On Sham Stimulation onset, the participant's fellow eye was occluded and the participant performed a reading task for 20 minutes.

Bilateral transcranial direct current stimulation consisted of 2 mA of current from the anodal electrode in the amblyopic primary visual cortex to the cathodal electrode located in the fellow primary visual cortex and the stimulation was on for 20 minutes. On stimulation onset, the participant's fellow eye was occluded and the participant performed a reading task for 20 minutes.

Outcomes

Primary Outcome Measures

Visual Acuity
Clarity or Sharpness in vision, measured in LogMar
Visual Sensitivity
The ability to perceive differences between an object and its background, measured in percentage of contrast sensitivity.
Stereopsis
the perception of depth produced by the reception in the brain of visual stimuli from both eyes in combination. Measured in degrees of arc.
Visual evoked potentials
The electroencephalographic response from the primary visual cortex to a stimuli. Measured in millivolts (mV).

Secondary Outcome Measures

Full Information

First Posted
August 13, 2021
Last Updated
August 20, 2021
Sponsor
University of Chile
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1. Study Identification

Unique Protocol Identification Number
NCT05016830
Brief Title
Bilateral Transcranial Direct Current Stimulation and Ocular Occlusion for Adults With Amblyopia
Official Title
Effect of the Combination of tDCS and Visual Occlusion Therapy on Visual Acuity, Contrast Vision and Depth Vision, in Adult Patients With Amblyopia
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Terminated
Why Stopped
Lock-down in the city of Santiago due to Covid-19 pandemia. Most faculty premises were closed for research purposes and mobility in the city was restricted.
Study Start Date
November 5, 2019 (Actual)
Primary Completion Date
January 31, 2020 (Actual)
Study Completion Date
January 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Chile

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A prospective interventional study is expected to be conducted, to test a possible new treatment for amblyopia (lazy eye syndrome). Bilateral transcranial direct current stimulation (tDCS) is a type of noninvasive brain stimulation, which may help in visual function recovery of adult patients with amblyopia. This pilot study will test the feasibility of said therapy, along with the short term effects of bilateral tDCS in visual function.
Detailed Description
Theoretical Framework: Ocular occlusion treatment has been used classically and with excellent results for the treatment of amblyopia in those under 14 years of age, since in this period it has been seen that there is greater neuroplasticity, leaving little to do in the period of lower neuroplasticity, in young and adult patients with later diagnoses. Transcranial Direct Current Stimulation therapy is an emergent technique used in neurological diseases to increase neuroplasticity, by changing the resting potential of neurons. Our hypothesis is that the combination of tDCS and visual occlusion therapy is capable of increasing visual acuity, contrast sensitivity, and depth perception, in young people over 18 years of age. Methodology: The application of a double-blind, randomized clinical trial is proposed to evaluate the application of 2 different therapies: Occlusion with bilateral tDCS, and Occlusion with tDCS sham (sham). The study subjects will be randomly assigned to a group, and one session of stimulation will be performed. Data will be analyzed using Student's t test, or Mann-Whitney test, according to the normal or non-normal distribution of the sample, respectively. Also, the change over time of the variables will be measured using the Conditional Change Model. Expected Results: The investigators expect that visual acuity, contrast vision, and dichoptic vision in the Occlusion therapy group with bilateral tDCS will be significantly higher than the Occlusion therapy group with tDCS sham (sham).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Amblyopia
Keywords
Lazy eye syndrome, Transcranial direct current stimulation, Ocular occlusion, Amblyopia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A randomized, controlled pilot trial, that consists in two groups: a control group that receives sham stimulation and ocular occlusion, and a second group that receives bilateral transcranial direct current stimulation and ocular occlusion.
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
Both sham and bilateral transcranial direct current stimulation were applied with the same electrode configuration, but the functioning of the stimulation device was blinded to the patient, the care provider, and the researcher performing measurements. The operator of the stimulation device selected the stimulation protocol. Sham stimulation protocol consisted of current ramp and delivery of current for 30 seconds and 19 minutes and 30 seconds with no current delivery. Actual stimulation consisted of a current ramp and 20 minutes of current delivery. There were no visual cues allowing to differentiate sham and stimulation protocols.
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sham bilateral transcranial direct current stimulation
Arm Type
Sham Comparator
Arm Description
Sham bilateral transcranial direct current stimulation consisted of 2 milliamperes (mA) of current from the anodal electrode in the amblyopic primary visual cortex to the cathodal electrode located in the fellow primary visual cortex, but the stimulation was turned off after 30 seconds. On Sham Stimulation onset, the participant's fellow eye was occluded and the participant performed a reading task for 20 minutes.
Arm Title
Bilateral transcranial direct current stimulation
Arm Type
Experimental
Arm Description
Bilateral transcranial direct current stimulation consisted of 2 mA of current from the anodal electrode in the amblyopic primary visual cortex to the cathodal electrode located in the fellow primary visual cortex and the stimulation was on for 20 minutes. On stimulation onset, the participant's fellow eye was occluded and the participant performed a reading task for 20 minutes.
Intervention Type
Device
Intervention Name(s)
Bilateral transcranial direct current stimulation
Intervention Description
A direct current is applied with two electrodes (cathode and anode) in specific parts of the skull. In this case the anode was over the occipital area to target the amblyopic cortex, while the cathode was over the contralateral side, targeting the fellow cortex.
Primary Outcome Measure Information:
Title
Visual Acuity
Description
Clarity or Sharpness in vision, measured in LogMar
Time Frame
1-2 hours
Title
Visual Sensitivity
Description
The ability to perceive differences between an object and its background, measured in percentage of contrast sensitivity.
Time Frame
1-2 hours
Title
Stereopsis
Description
the perception of depth produced by the reception in the brain of visual stimuli from both eyes in combination. Measured in degrees of arc.
Time Frame
1-2 hours
Title
Visual evoked potentials
Description
The electroencephalographic response from the primary visual cortex to a stimuli. Measured in millivolts (mV).
Time Frame
1-2 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Prior diagnosis of Amblyopia Exclusion Criteria: Ophthalmologic disease other than amblyopia Chronic pharmacological therapy Implanted medical device Neurologic disease or surgery history History of an adverse reaction to tDCS Pregnancy Not able to give informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Romulo A Fuentes Flores, PhD
Organizational Affiliation
University of Chile
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty of Medicine of University of Chile
City
Santiago
State/Province
Region Metropolitana
ZIP/Postal Code
8380453
Country
Chile

12. IPD Sharing Statement

Plan to Share IPD
No

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Bilateral Transcranial Direct Current Stimulation and Ocular Occlusion for Adults With Amblyopia

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