RECRUITING

Dynamic Versus Static Night Splinting of Plantar Fasciitis

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

Dynamic Versus Static Night Splinting of Plantar Fasciitis

Quick Facts

Study Start:2023-10-31
Study Completion:2025-06-18
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05432895

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Demographic - Over 18 years of age and ambulatory without a gait aid with no history of narcotic use
  2. * Diagnosis - Unilateral or bilateral acute (\< 6 months of pain) plantar fasciitis (i.e., Heel pain that increases with weightbearing, "First step pain": heel pain that occurs after a period of non-weightbearing, such as in the morning when arising from bed or when arising after prolonged sitting; the pain is improved after a few minutes walking but will worsen again with prolonged weightbearing, tenderness over the medial calcaneal tuberosity at the insertion of the plantar fasciitis)
  3. * Permitted - Icing, NSAIDS( ibuprofen), Custom Shoe Inserts, Diagnostic Ultrasound
  1. * Demographic - Under 18 year of age, requires a gait aid for ambulation; if not covered by insurance,
  2. * Diagnosis of - Arthritis of the Ankle, Midfoot, or Forefoot; Inflammatory Arthritis; Gout; Turf Toe; Hallux Rigidus; Hallux Limitus; Sesamoiditis; Tendonitis or Tendinopathy; Prior tear or Rupture of the Plantar Fascia; Fibromyalgia, Neuralgia, or Neuropathy; Peripheral Vascular Disease; Prior Trauma to the Heel, Fracture of the Calcaneus; Infection; Corn; Callus; Ingrown Nail.
  3. * Patient with history of Symptoms for over 6 months
  4. * Refractory to prior splint-based treatments
  5. * Prior injection of the plantar fascia
  6. * Prior surgery on the plantar fascia
  7. * Narcotic use

Contacts and Locations

Study Contact

Prerna Arora
CONTACT
6507217631
arprerna@stanford.edu

Study Locations (Sites)

Stanford University School of Medicine
Palo Alto, California, 94063
United States
Stanford outpatient center
Redwood City, California, 84063
United States

Collaborators and Investigators

Sponsor: Stanford University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-10-31
Study Completion Date2025-06-18

Study Record Updates

Study Start Date2023-10-31
Study Completion Date2025-06-18

Terms related to this study

Additional Relevant MeSH Terms

  • Plantar Fascitis