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Effects of radial extracorporeal shockwave therapy versus high intensity laser therapy in individuals with plantar fasciitis: a randomized clinical trial

Effects of radial extracorporeal shockwave therapy versus high intensity laser therapy in individuals with plantar fasciitis: a randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210125001
Enrollment
32
Registered
2021-01-25
Start date
2021-05-17
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Plantar Fasciitis patient plantar fasciitis, high intensity laser, shockwave

Interventions

The initial phase is a fast manual scanning along plantar aponeurosis with a total of 60 J. The intermediate phase, HILT will be applied on the most painful spot with a total energy of 30 J. The final
Experimental Device,Experimental Device
high intensity laser,Radial extracorporeal shockwave

Sponsors

Faculty of Physical Therapy
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: pain at medial calcaneal tuberosity, unilateral VAS more than 2 pain at the first step in the morning VAS more than 2 Age more than 18

Exclusion criteria

Exclusion criteria: Musculoskeletal disorders such as Tendo Achilles (TA) rupture, ankle osteoarthritis, prior surgery or metal implant at lower back and lower limb, acute plantar fasciitis or having severe pain (P10) or unable to bear weight or positive result of Ottawa s rule, pain medication within 1 week prior to participation, Red flags, precautions/contra-indications, and systemic diseases such as cancer, autoimmune disease, vascular disease or observable skin change, infected area, coagulation disorders, diabetes related, steroid (injection and oral), tattoo at lower limb Other considerations for patient s safety and confounding factors such as nerve or neurologic impairments, pregnancy BMI more than 30, physical or mental disorders

Design outcomes

Primary

MeasureTime frame
Pain pressure threshold at constant load 80 N baseline and every after treatment section Algometer

Secondary

MeasureTime frame
Pain at first step in the morning and after prolong resting baseline and every after treatment section VAS,Skin blood flow baseline and every after treatment section laser droppler flowmetry ,Skin temperature baseline and every after treatment section laser droppler flowmetry,Foot function index baseline and every after treatment section FFI questionaire,Plantar fascia thickness baseline and every after treatment section ultrasound diagnosis,Flexor digitorum brevis thickness baseline and every after treatment section ultrasound diagnosis

Countries

Thailand

Contacts

Public ContactChutiporn Thammajaree

Mahidol University

chutiporn.thm@mahidol.edu09339923924

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026