None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Running History: People who routinely run (e.g., 10 miles or more per week) Diagnosis: Plantar fasciitis was confirmed by a medical practitioner. The duration of symptoms is at least three months but no more than two years. No Major Comorbid Conditions: Participants should not have significant comorbidities that would confound the study results, such as severe osteoarthritis, neurological disorders, or uncontrolled diabetes, which could interfere with the rehabilitation process or influence plantar fasciitis outcomes. No Recent Foot/Ankle Surgery: Participants should not have undergone surgery on the foot or ankle in the past 6 months, as this could interfere with the recovery from plantar fasciitis or alter the mechanics of the foot. No Use of Orthotics or Assistive Devices: Ideally, participants should not be using custom orthotics or other assistive devices that alter foot mechanics, unless they have used them for a consistent period before enrollment, so as not to introduce variables into the study. Consent to Participate: Participants must be able to provide informed consent and have no psychological or cognitive barriers that would impede their participation or understanding of the study. Baseline Physical Function: Participants should have a baseline physical function that allows them to perform the prescribed stretching and strengthening exercises. This would exclude individuals with significant difficulty in performing basic exercises due to the pain or other physical impairments.
Exclusion criteria
Exclusion criteria: Exclusion Criteria: Recent injuries:- Any additional foot or lower extremity injuries within the last six months. Surgery History: Past ankle or foot operations for plantar fasciitis. Medical Conditions: Rheumatoid arthritis, diabetes, and other systemic foot disorders are examples of medical conditions. Pregnancy: Participants who are or intend to get pregnant during the study. Currently Receiving Treatment: Throughout the study period, receiving additional physical therapy or plantar fasciitis treatments Inability to follow protocol: - Participants who are unable or unwilling to comply with the study requirements, such as attending appointments or completing prescribed exercises.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Stretching and StrengtheningTimepoint: At Baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of LifeTimepoint: At Baseline | — |
Countries
India
Contacts
Galgotias University