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Textured Insoles to Restore Sensorimotor Function in Patients With Plantar Fasciopathy

Textured Insoles to Restore Sensorimotor Function in Patients With Plantar Fasciopathy

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07765082
Acronym
TIRE
Enrollment
26
Registered
2026-08-14
Start date
2026-09-01
Completion date
2027-07-01
Last updated
2026-08-14

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

Conditions

Plantar Fasciopathy

Brief summary

This study will evaluate the immediate effects of wearing textured insoles on gait, postural control, and sensorimotor function in adults with plantar fasciopathy. Researchers will compare functional performance while participants wear textured insoles to determine whether this intervention may improve stability, movement and future studies of longer-term treatment.

Detailed description

Plantar fasciopathy is a common condition that causes heel pain and is associated with impaired sensorimotor function, altered gait, reduced balance and decreased physical function. Current treatments primarily target symptom relief and do not directly address sensorimotor impairments. Textured insoles provide sensory stimulation to the plantar surface of the foot and may improve balance, gait mechanics and functional performance by enhancing plantar cutaneous input. This study will investigate the acute effects of textured insoles on gait, postural control and sensorimotor function in adults with plantar fasciopathy. Results will provide preliminary evidence regarding the feasibility and potential effectiveness of textured insoles as a treatment strategy and inform future studies evaluating longer-term outcomes.

Interventions

A textured shoe insole designed to provide plantar sensory stimulation by increasing cutaneous input to the foot during standing and walking.

OTHERSmooth Insole

A smooth shoe insole without surface texture used as a control device for comparison with the textured insole.

Sponsors

Jennifer Xu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of plantar fasciopathy for at least 3 months * Able to walk continuously at a self-selected pace for at least 20 minutes * Able and willing to provide informed consent

Exclusion criteria

* Concomitant lower extremity injury (example fracture) * History of lower extremity injury within the previous 6 months * History of hip, knee, or ankle surgery involving bones, joints, ligaments, tendons, or cartilage. * Any condition other than plantar fasciopathy that affects balance or plantar cutaneous sensation. * Neurological deficits, vestibular disorders, visual disturbances, or other conditions that impair movement or sensory function. * Pregnancy * Unable to speak or understand English.

Design outcomes

Primary

MeasureTime frameDescription
Change in Postural ControlBaseline and immediately following completion of each intervention condition during the study visitPostural control will be assessed while participants complete standardized balance testing under each study condition. Performance will be compared between the textured insole and smooth insole conditions to evaluate the acute effects of textured insoles on postural control.

Secondary

MeasureTime frameDescription
Change in Gait CharacteristicsBaseline and immediately following completion of each intervention condition during the study visit.Gait characteristics will be assessed during walking trials under each study condition and compared between the textured and smooth insole conditions.
Change in Plantar SensationBaseline and immediately following completion of each intervention condition during the study visit.Plantar sensation will be assessed with the Semmes-Weinstein monofilaments. The detection threshold will be the lightest weight monofilament (grams of force (gf)) that can be perceived by the participant. Lower values indicate better plantar sensation.
Change in Pressure-Pain ThresholdBaseline and immediately following completion of each intervention condition during the study visit.Pressure-pain threshold will be assessed with an algometer. The pressure-pain threshold will be measured in kg/cm2. Higher values indicate better pressure-pain threshold.

Countries

United States

Contacts

CONTACTJennifer Xu, PhD
jen.xu@uky.edu8593239850

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 15, 2026