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Active, not recruitingNCT07672327Blind assessorUpdated Jun 26, 2026

Efficacy of Short Wave and Laser Therapy in Patients With Plantar Fasciitis

An interventional study of conventional physical therapy and Extracorporeal shock wave therapy in Plantar Fasciitis, Chronic, sponsored by Ibrahim Abuomar Fadulaalhq Alramadhani. Active, not recruiting at 1 site in Saudi Arabia. Open to participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-06-26.

Sponsored by Ibrahim Abuomar Fadulaalhq Alramadhani · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
All
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Study summary

Plantar fasciitis is a common painful condition. It accounts for 10-15% of all foot painful conditions. Recently, Extracorporeal shock wave therapy (ESWT) was used as an effective method in treatment of different musculoskeletal disorders. High-intensity laser therapy (HILT) is a relatively recent treatment option that has shown benefits in a wide range of musculoskeletal disorders.

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Conditions studied

  • Plantar Fasciitis, Chronic

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03

In context

Fasciitis, Plantar

267 studies on the registry are indexed under Fasciitis, Plantar; 70 are open to participants now.

This study's planned enrollment of 60 is close to the median of 56 across 233 interventional studies indexed under Fasciitis, Plantar.

Browse Fasciitis, Plantar studies →

Lead sponsor

This is the only study on the registry with Ibrahim Abuomar Fadulaalhq Alramadhani as lead sponsor.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 1. Patients will be included according to the diagnostic criteria for plantar fasciitis of the American physical therapy association (APTA) (Martin et al., 2014). This criterion includes pain in medial sole and heel of foot: most pronounced in initial steps after a period of inactivity, it also worsens after prolonged weight bearing, pain during palpation and compression of proximal plantar fascia, limited range of motion in active and passive ankle dorsiflexion, positive windlass test.

    2. Patients will be referred from an orthopedic surgeon with confirmed diagnosis of plantar fasciitis (Bidoki et al., 2024).

    3. Patients with chronic plantar fasciitis (Duration of patient's symptoms will be more than three months) (Riaz et al., 2023).

    4. Patients' age will range from 18 to 45 years (Bidoki et al., 2024). 5. Both genders (Riaz et al., 2023). 6. Localized non radiating foot pain with an NPRS more than 5 on the first step in the morning (Riaz et al., 2023).

Exclusion criteria

Exclusion Criteria:

  • Patients will be excluded if they present any of the following criteria

    1. History of previous surgery of plantar fasciitis (Riaz et al., 2023).
    2. History of previous corticosteroid injections (Bidoki et al., 2024).
    3. History of heel pain due to previous trauma or calcaneus stress fracture in the last 3 months (Bidoki et al., 2024).
    4. History of previous lumbar spine surgery (Bidoki et al., 2024).
    5. History of rheumatologic disease (rheumatoid arthritis, diffuse idiopathic skeletal hyperostosis, systemic lupus erythematosus, gout, Sjogren disease, enthesopathy, etc…) (Bidoki et al., 2024).
    6. Pregnancy, pacemaker fitted or bleeding disorders (Bidoki et al., 2024).
    7. Wounds, infections or tumors in the treatment area (Bidoki et al., 2024).
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
Single (Participant)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Control group

    Group (A)

    Other: conventional physical therapy

  • Experimental
    Extracorporeal shock wave therapy

    Group (B)

    Other: Extracorporeal shock wave therapy

  • Experimental
    High-intensity laser therapy

    Group (C)

    Other: High-intensity laser therapy

Interventions

  • Otherconventional physical therapy

    exercise

  • OtherExtracorporeal shock wave therapy

    ESWT

  • OtherHigh-intensity laser therapy

    HILT

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What researchers measure

Primary outcomes

  1. Hand held dynamometer

    Hand held dynamometer is a portable device, characterized as a low-cost and convenience to assess muscle strength in a clinical setting

    Time frame: 6 weeks

  2. Ultrasonography

    Ultrasonography is a type of medical imaging device that uses high-frequency sound (ultrasound) waves to produce images of internal organs and other tissues such as tendons, muscles, joints, blood vessels, and internal organs, to measure some characteristics

    Time frame: 6 weeks

  3. Arabic version of foot function index (FFI-Ar)

    Foot functional index is a self-administered index consisting of 23 items divided into 3 subcategories on the basis of: pain, disability and activity limitation.

    Time frame: 6 weeks

  4. Arabic version of numerical pain rating scale (NPRS-Ar)

    The Numerical Rating Scale is an 11-point (0-10) Scale that measures pain intensity, it is considered a very sensitive pain assessment scale.

    Time frame: 6 weeks

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Study locations

1 site
  • Mecca
    Mecca, Mecca Region 24211, Saudi Arabia
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References and documents

Study documents

  • Protocol and informed consent form · Sep 25, 2025

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No — Because it is top secrets for them and they refused.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07672327
Lead sponsor
Ibrahim Abuomar Fadulaalhq Alramadhani
Responsible party
Ibrahim Abuomar Fadulaalhq Alramadhani (M. Sc. in Physical Therapy, Sport Physical Therapy (2021) College of Applied Medical Sciences, Umm Al-Qura University, Kingdom of Saudi Arabia, Umm Al-Qura University) — Sponsor-investigator
First posted
Jun 26, 2026
Start date
Jun 1, 2026
Primary completion
Jun 1, 2026
Completion
Jul 1, 2026 (estimated)
Last update
Jun 26, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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