Effect of different Insoles in patients with Plantar Fasciitis

Not Applicable

Recruiting

• Conditions: Plantar Fasciítis; C05.360

• Registration Number: RBR-9dbpb8n
• Lead Sponsor: niversidade Federal de São Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-02-13
• Last Update Posted: 29 May 2023
• Study Completion: 2023-12-30

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Participants must be between 30 and 65 years old, both sexes. Participants must present pain for at least twelve weeks and grading at least 3 on the numerical pain scale, in the following situations: in the first steps of the morning and on palpation at the insertion of the plantar fascia located in the medial tubercle of the calcaneus. In addition to at least one of the following criteria: pain after a period of inactivity; pain in the plantar fascia after a recent increase in activities beyond the usual; or Positive Windlass Test.

Exclusion Criteria

volunteers who have: Fibromyalgia; musculoskeletal and neuromuscular disorder of a systemic nature; have used custom insoles; have undergone physiotherapy sessions; and have presented musculoskeletal injuries in the lower limbs in the last six months.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Will be considered the primary outcome pain intensity in the 8th week after randomization, evaluated by the 11-point numerical pain scale. A change of 1 point, on this scale, between the initial assessment and the 8th week after randomization will be considered a clinically significant change.