ClinicalTrials.gg
RecruitingNCT07337317Updated May 1, 2026

Evaluating Stairway Designs for Individuals With Vision Impairment

An interventional study of Frequency of contrast marking on stair steps in Vision, Low and Mobility Limitation, sponsored by The University of Alabama in Huntsville. Recruiting at 1 site in United States. Open to participants aged 65 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-01.

Sponsored by The University of Alabama in Huntsville · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started Jan 2026; still recruiting 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
65
Allocation
Not applicable
Ages
65 Years and older
Sex
All
01

Study summary

The goal of this study is to learn if contrast frequency on step tread-edges influences foot clearance measures, a marker of fall risk, in older adults with and without visual impairments.

The main questions that aim to be answered are how foot clearance measures change across different frequencies of stair contrast, and how experiences and perceptions of different stair contrast frequencies are evaluated.

Researchers will compare individuals with and without visual impairments to see if contrast frequency on step tread-edges changes.

Participants will attend one visit during which their vision will be measured, and they will be asked to ascend and descend laboratory stairs at different contrast frequencies.

An optional second visit will entail a focus group meeting to better understand how contrast affects mobility in their home and everyday life.

02

Conditions studied

  • Vision, Low
  • Mobility Limitation

Keywords

  • older adults
  • impaired contrast sensivity
03

In context

Vision, Low

98 studies on the registry are indexed under Vision, Low; 23 are open to participants now.

This study's planned enrollment of 65 is close to the median of 60 across 78 interventional studies indexed under Vision, Low.

Browse Vision, Low studies →

Lead sponsor

This is the only study on the registry with The University of Alabama in Huntsville as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. ≥ Contrast sensitivity log 1.6 or greater
  2. travels independently in the community, including stairways > two times/week
  3. comfortable ascending and descending a stairway with rest time provided

Exclusion criteria

Exclusion Criteria:

  1. severe rheumatologic and or orthopedic diseases (e.g., awaiting joint replacement, active inflammatory disease)
  2. lower-limb injuries and/or recent joint replacements (e.g., hip fracture, hip, or knee replacement within six months of study enrollment)
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
65 participants (estimated)

Study arms

  • Experimental
    Intervention

    All participants will participate in the experimental arm, that involves a factorial model approach inwhich all participants will experience all eight conditions.

    Other: Frequency of contrast marking on stair steps

Interventions

  • OtherFrequency of contrast marking on stair steps

    Frequency of contrast marking on stair steps will be evaluated to determine how foot clearance, perceptions in older adults with and without impaired contrast sensivity

06

What researchers measure

Primary outcomes

  1. Toe clearance

    Toe, foot vertical clearance on stair steps

    Time frame: visit 1, through study completion, an average of 1 year

  2. Heel clearance

    heel, foot horizontal clearance on stair steps

    Time frame: visit 1, through study completion, an average of 1 year

  3. Frequency of <5mm toe clearances

    how often \<5mm toe clearances occur

    Time frame: visit 1, through study completion, an average of 1 year

  4. Frequency of <5mm heel clearances

    how often \<5mm toe clearances occur

    Time frame: visit 1, through study completion, an average of 1 year

Secondary outcomes

  1. Likert-Scale responses of contrast marking frequency conditions

    5-point range from strongly dislike to strongly like

    Time frame: visit 1, through study completion, an average of 1 year

  2. Perception responses of contrast marking frequency conditions

    Collected via auditory responses

    Time frame: visit 1, through study completion, an average of 1 year

07

Study locations

1 of 1 sites recruiting
  • University of Alabama in Huntsville
    Huntsville, Alabama 35899, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — We will archive our deidentified metadata to the Inter-University Consortium for Political and Social Research (ICPSR).

Supporting information: Study protocol, Analytic code

Time frame: The IDP will be made available within 6 months after publication, and will be made publicly available for 3 years.

Access criteria: Access will be monitored through ICPSR.

Data sharing details ↗ · www.openicpsr.org

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07337317
Lead sponsor
The University of Alabama in Huntsville
Responsible party
Sara Harper (Assistant Professor, The University of Alabama in Huntsville) — Principal investigator
First posted
Jan 13, 2026
Start date
Jan 22, 2026
Primary completion
Jan 2027 (estimated)
Completion
Jul 2027 (estimated)
Last update
May 1, 2026

Study contacts

Sara A Harper, PhD
Contact
sah0075@uah.edu
2568242184
Sara A Harper, PhD
principal investigator · University of Alabama in Huntsville

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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