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NCT06804512

Intermittent Visual Perturbations to Enhance Balance Training

Recruiting now EARLY_PHASE1 Last updated 10 February 2026
What this trial tests

EARLY_PHASE1 trial testing Visual Occlusion Goggles in Balance in 540 participants. Currently enrolling.

Timeline
20 August 2024
Primary endpoint
28 February 2029
28 February 2029

Quick facts

Lead sponsorUniversity of Florida
PhaseEARLY_PHASE1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposebasic science
Enrollment540
Start date20 August 2024
Primary completion28 February 2029
Estimated completion28 February 2029
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Florida

Who can join

Adults 18 to 89, any sex, with Balance. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this research study is to determine if intermittent visual perturbations can improve balance training. The investigators will quantify differences in body movement, muscle activity, and beam walking performance during and after practice walking on a balance beam that is 1" high. The investigators will ask the participants to come to the laboratory twice (2 sessions). The first session will not last more than 3 hours. The second session will not last more than 1 hour and will be two weeks after the first session. In total, the maximum amount of time the participant would be asked to participate is 4 hours.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Balance

Currently open trials in the same condition.

Other University of Florida trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06804512.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing