BridgeMD
New treatment option for Low Vision
Official title Wearable Echolocation Aids Using Parametric Sound
ClinicalTrials.gov ID: NCT07218991
What this study is testing
- What it's testing
- The objective of this study is to study a novel device designed to aid patients with impaired vision to safely navigate their environment. Subjects for this study will be individuals with normal vision, either with or without correction.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 100. Healthy volunteers may be eligible.
You may be able to join if
- Subject has provided informed consent in a manner approved by the Institutional Review Board (IRB) and is willing and able to comply with the trial...
- Adults at least 18 years of age and no older than 100 years of age at the time of consent.
- Individuals in good health who can perform daily activities without assistance and can walk independently.
- Normal vision (with or without corrective lenses) if there is no uncorrectable visual impairment.
You likely can't join if
- History of gait problems.
- Foot or leg impairments.
- Hearing impairment.
- Vertigo or other balance problems.
- Pregnant individuals.
- Any medical condition that, in the opinion of the investigator, would place the subject at increased risk for participation.
See the full eligibility criteria
- Subject has provided informed consent in a manner approved by the Institutional Review Board (IRB) and is willing and able to comply with the trial procedures.
- Adults at least 18 years of age and no older than 100 years of age at the time of consent.
- Individuals in good health who can perform daily activities without assistance and can walk independently.
- Normal vision (with or without corrective lenses) if there is no uncorrectable visual impairment.
- History of gait problems.
- Foot or leg impairments.
- Hearing impairment.
- Vertigo or other balance problems.
- Pregnant individuals.
- Any medical condition that, in the opinion of the investigator, would place the subject at increased risk for participation.
- Medications that may cause dizziness or weakness.
- Concurrent participation on another research study.
- Use of an investigational agent in the 30 days prior to signing informed consent.
- History of prior non-compliance.
- Presence or history of psychiatric condition (including anxiety, psychosis, drug, or alcohol addiction) that would, in the opinion of the investigator, make it difficult for the subject to comply with the study...
- Non-English-speaking individuals.
- Individuals from special or vulnerable populations (i.e., adults unable to consent, minors, incarcerated individuals).
- Body weight greater than 700 pounds.
The study team makes the final eligibility decision.
Where it's taking place
- Galveston, Texas, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 100 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Galveston, Texas, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.