Visual Training for Improving Intermittent Exotropia Visual Function

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-14
SponsorShanghai Eye Disease Prevention and Treatment Center

About this trial

The goal of this clinical tral is to investigate that if VR/AR visual training can improve the visual function in children with intermittent exotropia.

The main question it aims to answer is :

Does the VR/AR visual training can enhance stereoscopic vision function in children with intermittent exotropia.

Researchers will compare intervention group to control group to see if VR/AR visual training could enhance stereoscopic vision function in children with intermittent exotropia.

Participants will:

The intervention group will receive 20 minutes of VR/AR visual training once a day for a period of one year.

Follow up check ups at the hospital every 3 months. Keep a diary of the values of stereoscopic vision function and Newcastle Control Score.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • VR/AR visual training group

    Device

    Wear glasses for correction combined with VR/AR visual training in the first 6 months, and terminate the training for follow-up observation in the last 6 months. Regular follow-up every 3 months, with a total follow-up time of 1 year.

Treatment groups

78 Participants
are divided into 2 treatment groups
Group A: VR/AR visual training groupExperimental treatment 1 intervention
Group B: control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

changes in stereoscopic vision function after 6 month

Compare whether the intervention group has better stereoscopic vision function than the control group after 6 months

Time frame
6 months after baseline
2

changes in stereoscopic vision function after 12 month

Stop the intervention group training after 6 months and observe for another 6 months to see if there will be a decrease in stereoscopic vision function.

Time frame
12 month after baseline

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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