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Gait and Cognitive Function in Relation to Foot Arch Structure in Older Adults

Relationship Between Foot Arch Structure, Spatiotemporal Gait Parameters, and Cognitive Function in Older Adults

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07582367
Enrollment
50
Registered
2026-05-12
Start date
2026-04-15
Completion date
2026-11-08
Last updated
2026-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Function, Foot Biomechanics, Gait

Brief summary

This study aims to investigate the relationship between foot arch structure and spatiotemporal gait parameters and cognitive function in older adults. Foot arch integrity will be assessed using the Navicular Drop Test, and gait performance will be evaluated using the 10-Meter Walk Test. Cognitive-motor interaction will be examined through lower extremity reaction time using a light-based system. The study is designed as an observational cross-sectional analysis.

Interventions

OTHERObservational Assessment

This is an observational study with no intervention. Participants will undergo assessments of foot arch structure, gait parameters, and cognitive-motor performance.

Sponsors

Balikesir University
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Aged 65 years or older * Able to walk independently for at least 10 meters without assistive devices * Able to understand study procedures and provide informed consent * Having sufficient cognitive and physical capacity to comply with the assessment protocol

Exclusion criteria

* Diagnosed neurological disorders affecting gait and motor control (e.g., stroke, Parkinson's disease, multiple sclerosis) * Diagnosed dementia or Alzheimer's disease, or Mini-Mental State Examination (MMSE) score below 24 * Severe visual or hearing impairment that cannot be corrected and may affect reaction time testing * History of major lower extremity or spinal surgery within the last 6 months Severe musculoskeletal conditions affecting gait (e.g., advanced osteoarthritis, severe pain, active inflammation, open wounds, or recent fractures in the lower extremity) * Presence of severe balance disorders (e.g., vertigo)

Design outcomes

Primary

MeasureTime frameDescription
Gait Speed (m/s)Baseline (single session)Gait speed will be assessed using the 10-Meter Walk Test under comfortable walking conditions. Walking speed will be recorded in meters per second (m/s).
Cadence (steps/min)Baseline (single session)Cadence will be assessed using the 10-Meter Walk Test under comfortable walking conditions. Cadence will be recorded as steps per minute.
Step Length (m)Baseline (single session)Step length will be assessed using the 10-Meter Walk Test under comfortable walking conditions. Step length will be recorded in meters.
Double Support Time (%)Baseline (single session)Double support time will be assessed using the 10-Meter Walk Test under comfortable walking conditions. Double support time will be recorded as a percentage of the gait cycle.

Secondary

MeasureTime frameDescription
Lower extremity reaction timeBaseline (single session)Reaction time will be measured using a visual stimulus-based system (Light Trainer). The time between stimulus onset and foot contact response will be recorded in milliseconds. Multiple trials will be averaged to obtain the final value.
Navicular Drop Test (mm)Baseline (single session)Medial longitudinal arch mobility will be assessed using the Navicular Drop Test. The vertical displacement of the navicular tuberosity from seated subtalar neutral position to standing position will be measured in millimeters.

Countries

Turkey (Türkiye)

Contacts

CONTACTEbru Tekin, Lecturer
ebrutekin123@gmail.com+90 266 614 69 11

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 13, 2026