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Behavioral Intervention

Biofeedback Training for Improving Eye Focusing with Multifocal Lenses

N/A
Recruiting
Research Sponsored by State University of New York College of Optometry
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately before and after one episode of auditory biofeedback training. change in accommodation from the baseline will be assessed weekly for 3 weeks.
Awards & highlights

Study Summary

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.

Who is the study for?
This trial is for young adults aged 18-30 with no eye function issues, a specific range of nearsightedness (-0.75 D to -10 D), and good visual acuity. They must not have any eye diseases or be on medications that affect their eyesight or cause dry eyes.Check my eligibility
What is being tested?
The study tests if auditory biofeedback training can improve how well young adults' eyes adjust focus while wearing multifocal contact lenses designed for myopia control. It's split into three experiments based on the timing, repetition, and duration of the training.See study design
What are the potential side effects?
Since this trial involves non-invasive biofeedback training rather than medication, side effects are minimal but may include discomfort from wearing contact lenses longer than usual during the exercises.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately before and after one episode of auditory biofeedback training. change in accommodation from the baseline will be assessed weekly for 3 weeks.
This trial's timeline: 3 weeks for screening, Varies for treatment, and immediately before and after one episode of auditory biofeedback training. change in accommodation from the baseline will be assessed weekly for 3 weeks. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Accommodation

Trial Design

3Treatment groups
Experimental Treatment
Group I: The time course groupExperimental Treatment1 Intervention
The time course of the effect of biofeedback training in young adults wearing MFCLs. Subjects will receive one episode of auditory biofeedback training and accommodation will be measured before the training and after the training on a weekly basis for 3 weeks.
Group II: The repetition groupExperimental Treatment1 Intervention
Subjects will receive one episode of auditory biofeedback training every week for 3 weeks and accommodation will be measured before the training and after the training on a weekly basis.
Group III: The longer duration groupExperimental Treatment1 Intervention
Subjects will receive one episode of auditory biofeedback training for twice as long every week for 3 weeks and accommodation will be measured before the training and after the training on a weekly basis.

Find a Location

Who is running the clinical trial?

State University of New York College of OptometryLead Sponsor
19 Previous Clinical Trials
1,106 Total Patients Enrolled
2 Trials studying Accommodation
20 Patients Enrolled for Accommodation
William G. & Helen C. Hoffman FoundationUNKNOWN

Media Library

Auditory biofeedback training (Behavioral Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05684250 — N/A
Accommodation Research Study Groups: The time course group, The repetition group, The longer duration group
Accommodation Clinical Trial 2023: Auditory biofeedback training Highlights & Side Effects. Trial Name: NCT05684250 — N/A
Auditory biofeedback training (Behavioral Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05684250 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

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."

Answered by AI

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."

Answered by AI

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."

Answered by AI

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."

Answered by AI
~0 spots leftby May 2024