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Clinical Trial Summary

The goal of this clinical trial is to learn if a mobile application works to improve adherence to acupressure therapy in asthenopia. It will also learn about the efficacy of acupressure as a therapy for asthenopia. The main questions it aims to answer are: -Does a mobile application have a role to improve therapy compliance and efficacy of self-guided acupressure in asthenopia? Researchers will compare users of a mobile app to non-users of a mobile app to see if a mobile app works to improve adherence to acupressure therapy in asthenopia Participants will: - Do acupressure 2 times every day for 4 weeks - Filling in the absence link has been after doing acupressure every day - Fill out the link regarding the condition of asthenopia once per week


Clinical Trial Description

This is a clinical trial study to evaluate the role of a mobile application in therapy compliance and acupressure efficacy in asthenopia sufferers. Participants are 60 males/females aged 18-64 years. They will be divided into 2 groups: (1) Acupressure mobile app users and (2) Non-acupressure mobile app users. Acupressure is scheduled 2 times every day for 4 weeks. Therapy compliance will be assessed from the absence link that participants fill out every day, while therapy efficacy will be assessed once per week for 4 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06418191
Study type Interventional
Source Indonesia University
Contact Dion Rukmindar, MD
Phone +6285217264132
Email dion.rukmindar@ui.ac.id
Status Not yet recruiting
Phase N/A
Start date June 2024
Completion date July 2024

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