This trial will study how to improve accommodation in young adults wearing multifocal contact lenses to treat myopia, using auditory biofeedback training. It will assess the effect of training duration and repetition.
1 Primary · 0 Secondary · Reporting Duration: Immediately before and after one episode of auditory biofeedback training. Change in accommodation from the baseline will be assessed weekly for 3 weeks.
3 Treatment Groups
The time course group
1 of 3
The repetition group
1 of 3
The longer duration group
1 of 3
30 Total Participants · 3 Treatment Groups
Primary Treatment: The time course group · No Placebo Group · N/A
Who is running the clinical trial?
Age 18 - 30 · All Participants · 8 Total Inclusion CriteriaMark “Yes” if the following statements are true for you:
Frequently Asked Questions
Is the eligibility criteria for this study restricted to those under twenty years of age?
"This research project is looking for participants aged 18 years and above, however no older than 30." - Anonymous Online Contributor
Are there any vacancies available for participants in this research project?
"Affirmative. Clinicaltrials.gov's records demonstrate that the medical trial is presently enrolling patients; it was first posted on July 19th 2022 and recently updated on January 11th 2023. 30 individuals must be recruited from 1 site to complete this clinical experiment." - Anonymous Online Contributor
How many participants are being observed in this research endeavor?
"Affirmative. According to clinicaltrials.gov, the research project that was initially posted on July 19th 2022 is currently recruiting participants. A total of 30 patients are needed for this study at one specific medical centre and the most recent update was made on January 11th 2023." - Anonymous Online Contributor
Is it permissible for me to join this research experiment?
"This study is calling for 30 participants to meet the following criteria: acceptable monocular Snellen visual acuity (VA) of 20/25 or higher, age between 18-30 years old, refractive error within -0.75 D and -10 D range, astigmatism below 0.75D, appropriate accommodative amplitude in relation to their age group; no suspicious eye conditions (as reported by patients), normal binocular functions alongside requisite consent from each individual before enrolment into this trial." - Anonymous Online Contributor