Comparative of home and clinical interventions on plantar fasciitis

Not Applicable

• Conditions: plantar fasciitis.; Plantar fascial fibromatosis; M72.2

• Registration Number: IRCT20210207050275N1
• Lead Sponsor: Shiraz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 11 January 2022

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Inflammation of the plantar fascia
No surgery or fracture in the last month

Exclusion Criteria

Reluctance to participate in the study
People who have diseases that cause pain and inflammation in the foot

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Pre intervention, 3,6,9,12,15,18,21 days after intervention. Method of measurement: pain analog scale.;Hypersensivity. Timepoint: Pre intervention, 3,6,9,12,15,18,21 days after intervention. Method of measurement: Numeric Analog Scale, Mcgill Pain Questionnaire.