Multi-sensory rehabilitation program for people with ultra low vision
Development of a Multi-sensory Rehabilitation Program for People With Ultra Low Vision
This study tests a new rehabilitation program that uses different senses to help people with very low vision improve their everyday functioning and quality of life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 36 (estimated) |
| Ages | 12 Years to 99 Years |
| Sex | All |
| Sponsor | State University of New York College of Optometry Academic / other |
| Locations | 1 site (New York, New York) |
| Trial ID | NCT05028712 on ClinicalTrials.gov |
What this trial studies
This research aims to fill a significant gap in vision rehabilitation for individuals with profound visual impairment by evaluating a multi-sensory approach. The study will focus on developing a rehabilitation program that incorporates visual information training and multimodal training to enhance functional vision. By addressing the rehabilitation needs of patients with ultra low vision, the study seeks to improve their quality of life and maximize the efficacy of existing treatments for end-stage eye diseases.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals with ultra low vision, defined as having a visual acuity of 20/1600 or worse.
Not a fit: Patients who are under 12 years of age, dependent on a sighted guide, or have cognitive impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly enhance the quality of life for patients with ultra low vision by improving their functional vision.
How similar studies have performed: While there are growing numbers of clinical trials focusing on end-stage eye diseases, this multi-sensory approach is relatively novel and has not been extensively tested in this specific context.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * People with ultra low vision (visual acuity ≤20/1600) Exclusion Criteria: * \<12 years of age * dependent on sighted guide * cognitive impairment
Where this trial is running
New York, New York
- SUNY College of Optometry — New York, New York, United States (Recruiting)
Study contacts
- Principal investigator: Arathy Kartha, PhD — State University of New York College of Optometry
- Study coordinator: Arathy Kartha, PhD
- Email: akartha@sunyopt.edu
- Phone: 4243981727
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.