Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
All Genders
NCT05432895

Dynamic Versus Static Night Splinting of Plantar Fasciitis

Led by Stanford University · Updated on 2025-06-15

200

Participants Needed

2

Research Sites

137 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The investigators are trying to study that there is no difference in improvement of motion between static progressive and dynamic splinting.

CONDITIONS

Official Title

Dynamic Versus Static Night Splinting of Plantar Fasciitis

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Over 18 years of age and able to walk without a walking aid
  • Diagnosed with unilateral or bilateral acute plantar fasciitis with less than 6 months of pain
  • Heel pain that worsens with weightbearing and tenderness over the medial calcaneal tuberosity
  • Allowed use of icing, NSAIDs (ibuprofen), custom shoe inserts, and diagnostic ultrasound
Not Eligible

You will not qualify if you...

  • Under 18 years of age or requires a walking aid for ambulation
  • Diagnosed with arthritis of the ankle, midfoot, or forefoot; inflammatory arthritis; gout; turf toe; hallux rigidus or limitus; sesamoiditis; tendonitis or tendinopathy
  • Prior tear or rupture of the plantar fascia
  • Fibromyalgia, neuralgia, neuropathy, peripheral vascular disease
  • Prior heel trauma or calcaneus fracture
  • Infection, corn, callus, or ingrown nail
  • Symptoms lasting over 6 months
  • Unresponsive to previous splint treatments
  • Prior injection or surgery on the plantar fascia
  • Current use of narcotic medications

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Stanford University School of Medicine

Palo Alto, California, United States, 94063

Actively Recruiting

2

Stanford outpatient center

Redwood City, California, United States, 84063

Actively Recruiting

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Research Team

P

Prerna Arora

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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