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Accommodation-Related Visual Training Combined with Transcranial Electrical Stimulation Versus Visual Training Alone for the Treatment of Accommodation Dysfunction

ConditionsPresbyopiaEsotropia
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorEye & ENT Hospital of Fudan University

About this trial

This is a single-center, randomized controlled trial to compare the effectiveness of transcranial electrical stimulation combined with visual training with visual training alone for the treatment of accommodation disorder patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Inclusion criteria for small-angle acute concomitant esotropia: clinical diagnosis of acute aquired concomitant esotropia; strabismus angle ≤ 15PD; age 18 < age < 40; best corrected visual acuity of both eyes ≥ 1.0.

Inclusion criteria for presbyopia: clinical diagnosis of presbyopia; best corrected visual acuity of both eyes ≥ 1.0.

Disqualifiers

no history of other eye diseases or eye surgeries

no history of neuropsychiatric diseases for the individual or relatives

no head injuries or surgeries

no history of epilepsy or stroke

Trial design

Design model

Parallel

Treatments tested in this trial

  • Transcranial Electrical Stimulation

    Device

    Transcranial Electrical Stimulation Combined with Accommodation-related Visual Training

  • Visual Training

    Other intervention

    Accommodation-related Visual Training

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Transcranial Electrical Stimulation GroupExperimental treatment 1 intervention
Group B: Visual Training GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Amplitude of Accommodation

using minus lens method to evaluate amplitude of accommodation

Time frame
Before treatment, 1 week, 1 month, 3 months, 6 months after treatment
2

Accommodation Response

using binocular cross-cylinder method to evaluate accommodation response

Time frame
Before treatment, 1 week, 1 month, 3 months, 6 months after treatment
3

Positive and negative relative accommodation

using phoropter examination to evaluate positive and negative relative accommodation

Time frame
Before treatment, 1 week, 1 month, 3 months, 6 months after treatment
4

Accommodation Facility

Using flipper to evaluate the accommodation facility

Time frame
Before treatment, 1 week, 1 month, 3 months, 6 months after treatment

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Eye & ENT Hospital of Fudan University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: