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Effect of extracorporeal shock wave (ESWT) therapy on chronic plantar fasciitis.

Investigation the effect of extracorporeal shock wave therapy on pain and quality of life in patients with chronic plantar fasciitis.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016070118754N4
Enrollment
30
Registered
2016-12-10
Start date
2016-11-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Plantar fascitis. Plantar fascial fibromatosis

Interventions

Intervention 1: Intervention group: Using of shock waves on pain area of the painful heel and stretching plantar fascia and calf muscles of painful side. Intervention 2: Control group: stretching plan
Rehabilitation
Intervention group: Using of shock waves on pain area of the painful heel and stretching plantar fascia and calf muscles of painful side.
Control group: stretching plantar fascia and calf muscles of painful side.

Sponsors

Iran University of Medical Sciences, Vice chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with plantar fasciitis who have a history of pain at one heel region for more than 4 months with unsuccessful response to some kinds of conservative treatments such as NSAIDs, physiotherapy, stretching exercises and corticosteroids injections; increasing the heel pain with direct pressure on medial tuberosity of the calcaneus; a pain score equal and more than 5 based on visual analog scale (VAS) during the first steps of walking immediately after waking up in the morning; in the absence of any contraindication for shock wave therapy; in the absence of any observable deformity in lower extremity or spines and lower extremity discrepancy in clinical evaluation; in the absence of diabetes; in the absence of pregnancy. Exclusion criteria: if the patient dose not cooperation with therapist; if the patient starts any other treatment for plantar fasciitis along with present study; if patient does not complete the treatment sessions or does not participate in the regular study treatment program.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Plantar fascitiis. Timepoint: Before starting the treatment and after 4 weeks. Method of measurement: Visual analog scale, functional test, quality of life questionnaire.

Secondary

MeasureTime frame
Pain. Timepoint: At the beginning of therapy, 4 weeks after first session. Method of measurement: Visual analog scale.;Quality of life. Timepoint: At the beginning of therapy, 4 weeks after the first session and one month after ending the treatment. Method of measurement: Foot and ankle outcome score (FAOS).;Timed up and go. Timepoint: At the beginning of therapy, 4 weeks after first session. Method of measurement: Timed up and go functional test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJavad Sarrafzadeh

School of Rehabilitation Sciences, Iran University of Medical Sciences

sarrafzadeh.j@iums.ac.ir and j.sarrafzadeh@gmail.com+98 21 2222 8051

Outcome results

None listed

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