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

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

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190715044216N6
Enrollment
30
Registered
2022-02-10
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-03-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Posterior Tibial Tendon Dysfunction. Posterior tibial tendinitis

Interventions

Intervention 1: Intervention group 1:will perform posterior tibialis exercise with ankle in planter flexion and eversion in supine lying position +heating packs for 20 minutes and A Thera-band will b

Sponsors

Riphah International University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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).

Countries

Pakistan

Contacts

Public ContactMuhammad Jabbar

Riphah International University

drabduljabbar743725@gmail.com+92 348 4266429

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026