comparison of concentric and eccentric progressive resistive exercises on pain and disability in posterior tibial tendon dysfunctio

Phase 3

Recruiting

• Conditions: Posterior Tibial Tendon Dysfunction.; Posterior tibial tendinitis; M76.82

• Registration Number: IRCT20190715044216N6
• Lead Sponsor: Riphah International University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 8 March 2022

Recruitment & Eligibility

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

Inclusion Criteria

Age: 40–60 years •
Current complaint of foot and ankle pain that has lasted for three months or more
Flexible pes planovalgus deformity in the clinical assessment
Pes planovalgus foot deformity with longitudinal arch flattening verified by radiograph

Exclusion Criteria

Rigid foot deformity
Acute infection or alcohol addiction limiting participation in study protocol Acute use of local or systemic analgesics
Acute overuse or traumatic injury to the lower leg (excluding pes planovalgus associated pathology)
Prior surgery to the lower limb

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Intervention treatment will be given to subjects 2 sessions per week and 2 sets per day, 1 set in clinical setup and 2nd for home plan. Total intervention period will be of 6 weeks. Method of measurement: Pain Disability Index (PDI).;Disability. Timepoint: Intervention treatment will be given to subjects 2 sessions per week and 2 sets per day, 1 set in clinical setup and 2nd for home plan. Total intervention period will be of 6 weeks. Method of measurement: Numeric Pain Rating Scale (NPRS).