Shock Wave Therapy Versus Low Level Laser Therapy in Patients With Plantar Fasciitis

Plantar Fascitis Clinical Trial

Official title:

Effect of Shock Wave Therapy Versus Low Level Laser Therapy in Patients With Plantar Fasciitis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05867888
• Other study ID #: P.T.REC/012/004154
• Status: Completed
• Phase: N/A
• Start date: May 1, 2023
• Est. completion date: October 10, 2023

Study information

• Verified date: February 2024
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Both shock wave therapy and low level laser therapy in plantar fasciitis are effective in improvement of such cases without any side effects but there are no previously published studies on the use of shock wave therapy versus low level laser therapy in plantar fasciitis and, hence, evidence of its acceptability and effectiveness compared with each other remains to be established.

Description:

Plantar fasciitis is a result of degenerative irritation of the plantar fascia origin at the medial calcaneal tuberosity of the heel as well as the surrounding perifascial structures, it is a common problem accounting for approximately one million patient visits per year, it is often an overuse injury. As a result tight gastrocnemius, soleus, and/or other posterior leg muscles have also been commonly found in patients with this condition.

Shock wave therapy is thought to provide long lasting analgesia and stimulate the healing process, Low level laser therapy has been used to relieve pain caused by plantar fasciitis, also stretching of the shortened and contracted plantar flexors may positively influence an individual's functional activities of daily living and decrease the risk of injury.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 75
• Est. completion date: October 10, 2023
• Est. primary completion date: October 10, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 60 Years

Eligibility

Inclusion Criteria:

1. Age ranges from 40-60 years old.

2. Both genders will be included.

3. Unilateral plantar fasciitis.

4. Duration of symptoms more than 4 weeks.

5. Positive Windlass test and negative Tinel and calcaneus squeeze tests.

6. Patients will be classified according to their BMI (18.5 - 24.9) kg/m2

Exclusion Criteria:

1. Open wound, infection in plantar surface of foot.

2. History of foot surgery.

3. History of trauma or fracture in foot or ankle.

4. Neuropathic pain as diabetes mellitus.

5. Peripheral vascular disease.

6. Calcaneal stress fracture or show evidence of a foreign body or tumor of the affected heel.

7. Previously suffered a rupture or surgery of the plantar fascia. Existing or prior osteomyelitis of the involved calcaneus.

Related Conditions & MeSH terms

• Fasciitis
• Fasciitis, Plantar
• Plantar Fascitis

Intervention

Other:
• conventional therapy
conventional therapy ( instructions, ice application, deep tissue massage, stretching exercises, joint mobilization and isometric exercises )
• shock wave therapy
Acoustic waves (shock waves) that can carry energy and can propagate through tissues promote healing effects.
• low level laser therapy
The application of light to a biologic system to promote tissue regeneration, reduce inflammation and relieve pain.

Locations

Country	Name	City	State
Egypt	Reham	Giza

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assess the change in pain intensity level	The visual analogue scale (VAS) is a widely utilized pain intensity level assessment instrument in patients with plantar fasciitis. The visual analogue scale (VAS) is typically composed of a horizontal line from zero (minimum value) to 10 (maximum value) where zero signifies (no pain) and 10 signifies (worst pain) one can imagine.	Before treatment and after 6 weeks treatment
Primary	Assess the change in pain pressure threshold	Pressure algometry will be used to evaluate the pain pressure threshold for the two predetermined locations on the affected leg: gastrocnemius (middle point over the muscle belly) and soleus (center point of the muscle belly 10 cm above the Achilles tendon). The participant will speak up at the point where the pressure evoke a painful sensation. This process will be repeated 3 times in the same manner, and three measurements will be recorded at the same point on the plantar fascia. An average of the three readings will be recorded. Higher algometer scores indicate greater pressure threshold, therefore less tenderness. Lower algometer scores indicate less pressure threshold, thus more tenderness.	Before treatment and after 6 weeks treatment
Primary	Assess the change in range of ankle motion	Ankle range of motion (ROM) will be measured by using digital goniometer (ankle dorsiflexion and plantarflexion ranges will be measured). It can monitor the progress of intervention.	Before treatment and after 6 weeks treatment
Primary	Assess the change in foot functional disability	Foot functional disability will be assessed by foot and ankle ability measure questionnaire (FAAM). Higher scores on the questionnaire indicate a higher level of physical functioning and lower scores on the questionnaire indicate a lower level of physical functioning.	Before treatment and after 6 weeks treatment
Primary	Assess the change in ankle stability	The Human Assessment Computer (HUMAC) Balance System will be used in the current study to assess limits of stability of ankle joint.	Before treatment and after 6 weeks treatment