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Shockwave Therapy for Plantar Fasciitis RCT

Primary Purpose

Plantar Fascitis

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Radial shockwave therapy
Focused shockwave therapy
Shockwave therapy device
Home therapy
Sponsored by
Hospital for Special Surgery, New York
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Plantar Fascitis

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients presenting with a clinical diagnosis of chronic plantar fasciitis (>3 months) that has been recalcitrant to other treatments
  • Minimum VAS pain of 40/100 (4/10; morning pain when taking first steps, pain after prolonged walking/standing)
  • English-speaking

Exclusion Criteria:

  • Cortisone injection within the past 3 months
  • Platelet-rich plasma injection within the past 6 months
  • History of previous foot surgery
  • Bilateral heel pain
  • Coagulopathies or use of anti-coagulants
  • Local and systemic neurologic or vascular insufficiencies
  • Rheumatologic disorders
  • Systemic inflammatory disorders
  • Active or chronic infection in the area
  • Lower extremity bone disorders (e.g., Paget's disease, osteomyelitis)
  • Calcaneal fractures
  • Nerve entrapment
  • Ruptures in tendon
  • Non-English speaking

Sites / Locations

  • Hospital for Special Surgery

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Control

Radial shockwave therapy

Focused shockwave therapy

Arm Description

Patients in the control group will be treated using the home therapy protocol only.

Patients will receive 4 sessions of radial shockwave therapy.

Patients will receive 4 sessions of focused shockwave therapy.

Outcomes

Primary Outcome Measures

Visual analog scale pain - morning
Morning pain. This will be assessed on a scale of 0-100, with a higher score representing more pain.
Visual analog scale pain - after prolonged walking or standing
Pain after prolonged walking or standing. This will be assessed on a scale of 0-100, with a higher score representing more pain.

Secondary Outcome Measures

PROMIS Physical Function computer adaptive test score
This computer adaptive questionnaire assesses physical function. A higher score represents higher function. A score of 50 represents the population average.
Foot and Ankle Outcome Score (FAOS)
The FAOS assess pain, symptoms, activities of daily living, sports, and quality of life related to foot and ankle pain. This will be assessed on a scale of 0-100, where 100 indicates no problems and 0 indicates extreme problems.
Treatment satisfaction
Satisfaction with the assigned treatment will be determined on a 0-10 scale, with 10 being most satisfied and 0 being least satisfied.

Full Information

First Posted
March 11, 2020
Last Updated
March 17, 2023
Sponsor
Hospital for Special Surgery, New York
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1. Study Identification

Unique Protocol Identification Number
NCT04332471
Brief Title
Shockwave Therapy for Plantar Fasciitis RCT
Official Title
Treatment of Plantar Fasciitis With Radial Shockwave Therapy vs. Focused Shockwave Therapy: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 1, 2020 (Actual)
Primary Completion Date
March 1, 2024 (Anticipated)
Study Completion Date
April 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital for Special Surgery, New York

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
Inflammation of the plantar fascia is known as plantar fasciitis and is commonly seen in active or overweight individuals. It can be treated via conservative or surgical therapies. Extracorporeal shockwave therapy has shown promise in the treatment of plantar fasciitis. Several studies have compared the effects of different types of extracorporeal shockwave therapy (radial and focused) with other forms of conservative treatment in patients with chronic plantar fasciitis. No study has yet compared the effect of radial vs. focused shockwave therapy on pain in this population.
Detailed Description
Plantar fasciitis is a common foot problem that affects 3.8 per 1,000 persons in the United States. It is characterized by inflammation of the plantar fascia, a fibrous tissue which connects the calcaneus to the metatarsal heads, and is often seen in individuals who are overweight and/or participate frequently in weight-bearing endurance activities such as running. Pain is typically at its highest during the first steps in the morning, although it can also occur with prolonged weightbearing. Plantar fasciitis can be treated via conservative or surgical measures, although surgery is considered as the last resort. In recent years, extracorporeal shockwave therapy has emerged as an alternative conservative method for treating plantar fasciitis. There are two types -- radial and focused shockwave therapy. Focused therapy creates deeper-penetrating, higher-energy shockwaves, whereas radial therapy produces more superficial shockwaves that can treat a wider area of pathology. Randomized controlled trials have compared focused and radial shockwave therapy to placebo and other conservative measures in the treatment of chronic plantar fasciitis and overall demonstrated benefit. Only one study has directly compared radial and focused shockwave therapy in this population, although pain was not an outcome of focus in the study. The current study aims to collect patient-reported outcomes on both pain and function following radial vs. focused shockwave therapy vs. control therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Plantar Fascitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
114 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Active Comparator
Arm Description
Patients in the control group will be treated using the home therapy protocol only.
Arm Title
Radial shockwave therapy
Arm Type
Active Comparator
Arm Description
Patients will receive 4 sessions of radial shockwave therapy.
Arm Title
Focused shockwave therapy
Arm Type
Active Comparator
Arm Description
Patients will receive 4 sessions of focused shockwave therapy.
Intervention Type
Procedure
Intervention Name(s)
Radial shockwave therapy
Intervention Description
Target intensity will be within a range of 3.5-5.0 bar at maximum Hz, titrated up to patient tolerance within 100 pulses. Total of 3000 pulses.
Intervention Type
Procedure
Intervention Name(s)
Focused shockwave therapy
Intervention Description
Target intensity will be within a range of 0.15-0.25 mJ/mm2 at maximum Hz, titrated up to patient tolerance within 100 pulses. Total of 3000 pulses.
Intervention Type
Device
Intervention Name(s)
Shockwave therapy device
Intervention Description
The shockwave therapy device will be used to administer either radial or focused shockwave therapy.
Intervention Type
Other
Intervention Name(s)
Home therapy
Intervention Description
Stretching and ice massage
Primary Outcome Measure Information:
Title
Visual analog scale pain - morning
Description
Morning pain. This will be assessed on a scale of 0-100, with a higher score representing more pain.
Time Frame
Up to 1 year
Title
Visual analog scale pain - after prolonged walking or standing
Description
Pain after prolonged walking or standing. This will be assessed on a scale of 0-100, with a higher score representing more pain.
Time Frame
Up to 1 year
Secondary Outcome Measure Information:
Title
PROMIS Physical Function computer adaptive test score
Description
This computer adaptive questionnaire assesses physical function. A higher score represents higher function. A score of 50 represents the population average.
Time Frame
Up to 1 year
Title
Foot and Ankle Outcome Score (FAOS)
Description
The FAOS assess pain, symptoms, activities of daily living, sports, and quality of life related to foot and ankle pain. This will be assessed on a scale of 0-100, where 100 indicates no problems and 0 indicates extreme problems.
Time Frame
Up to 1 year
Title
Treatment satisfaction
Description
Satisfaction with the assigned treatment will be determined on a 0-10 scale, with 10 being most satisfied and 0 being least satisfied.
Time Frame
Up to 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients presenting with a clinical diagnosis of chronic plantar fasciitis (>3 months) that has been recalcitrant to other treatments Minimum VAS pain of 40/100 (4/10; morning pain when taking first steps, pain after prolonged walking/standing) English-speaking Exclusion Criteria: Cortisone injection within the past 3 months Platelet-rich plasma injection within the past 6 months History of previous foot surgery Bilateral heel pain Coagulopathies or use of anti-coagulants Local and systemic neurologic or vascular insufficiencies Rheumatologic disorders Systemic inflammatory disorders Active or chronic infection in the area Lower extremity bone disorders (e.g., Paget's disease, osteomyelitis) Calcaneal fractures Nerve entrapment Ruptures in tendon Non-English speaking
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kristina Quirolgico, MD
Organizational Affiliation
Hospital for Special Surgery, New York
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital for Special Surgery
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States

12. IPD Sharing Statement

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Shockwave Therapy for Plantar Fasciitis RCT

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