Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
Healthy Volunteers
ID07337317

Frequency of Contrast Enhancement on Stairways to Study Foot Clearance and Fall Risk in Older Adults with and without Vision Impairment

Led by The University of Alabama in Huntsville · Updated on 2026-05-01

65

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to understand how different frequencies of contrast markings on stair edges influence foot clearance, which is a key factor in fall risk, in older adults both with and without visual impairments. The study compares these two groups to see how stair contrast frequency affects their foot clearance measures and perceptions of stair safety. All participants will experience eight different stair contrast frequency conditions during one visit. They will walk up and down laboratory stairs while their vision is measured and their foot clearance is recorded under each condition. An optional second visit includes a focus group discussion to explore how stair contrast impacts their daily mobility at home. Participants will be assessed for toe and heel clearance, including how often their foot clearance is less than 5mm, throughout the study period averaging one year. Researchers will also collect participants' responses using rating scales and perception surveys regarding the stair contrast conditions. The study involves a single visit with an optional follow-up group meeting, focusing on mobility and safety measures.

CONDITIONS

Brief Title

Evaluating Stairway Designs for Individuals With Vision Impairment

Who Can Participate

Age: 65Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Contrast sensitivity log 1.6 or greater
  • Travels independently in the community, including stairways more than two times per week
  • Comfortable ascending and descending a stairway with rest time provided
Not Eligible

You will not qualify if you...

  • Severe rheumatologic and/or orthopedic diseases (e.g., awaiting joint replacement, active inflammatory disease)
  • Lower-limb injuries and/or recent joint replacements (e.g., hip fracture, hip or knee replacement within six months of enrollment)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Intervention

Duration - Approximately 1 year

Participants experience all eight conditions involving different frequencies of contrast marking on stair steps to evaluate foot clearance and perception.

Visits starting at baseline and continuing through study completion over about 1 year

Trial Site Locations

Total: 1 location

1

University of Alabama in Huntsville

Huntsville, Alabama, United States, 35899

Actively Recruiting

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Research Team

S

Sara A Harper, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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