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The effect of therapeutic tecar on pain and dorsiflexion range of motion in amateur athletes with plantar fasciitis

The effect of therapeutic tecar on gastrosoleus, achilles tendon and plantar fascia on pain and dorsiflexion range of motion in amateur athletes with plantar fasciitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180728040618N8
Enrollment
26
Registered
2024-12-09
Start date
2025-01-03
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Plantar fasciitis. Other soft tissue disorders related to use, overuse and pressure

Interventions

Intervention 1: Intervention group: The intervention group receives the treatment for 20 minutes using the TECAR 3 Winback device produced in France. In this way, the patient is placed on the bed in a

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: People between 18 and 50 years old who exercises at least 4 hours a week. people who have a primary clinical diagnosis of plantar fasciitis determined by tenderness to pressure on the medial tubercle of the calcaneus, as well as a complaint of heel pain associated with first step after walking in the morning greater than 3 on a visual analogue scale (VAS) at least three months.

Exclusion criteria

Exclusion criteria: Any systemic inflammatory and autoimmune disorders Any history of surgery, trauma, and fracture in the lower limbs Corticosteroid injection in the last 6 months for plantar fascia damage Patients with any contraindications for TECAR such as pregnancy, the presence of malignant tissue, tumors, in the ankle and foot, electrical devices implanted in the body, local sensory impairment, local vascular disease, and severe osteoporosis The patient's unwillingness to participate in the study

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before the intervention and 48 hours after treatment. Method of measurement: Visual analog scale.

Secondary

MeasureTime frame
Active range of motion of ankle dorsi flexion. Timepoint: Before the intervention and 48 hours after the treatment session. Method of measurement: goniometer.;Weight bearing lunge test. Timepoint: Before the intervention and 48 hours after the treatment session. Method of measurement: tape measure.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactIran University of Medical Sciences

Iran University of Medical Sciences

mohsenifarpt@gmail.com+98 21 2222 7124

Outcome results

None listed

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