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Shock Wave Therapy: Do the External Appearance of the Device Influence Clinical Outcomes?

Primary Purpose

Plantar Fasciitis, Pain

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
Standard shock waves device
Austere shock waves device
Sophisticated shock waves device
Sponsored by
Asociacion Colaboracion Cochrane Iberoamericana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Plantar Fasciitis focused on measuring shock wave, plantar fasciitis, placebo effect, nocebo effect

Eligibility Criteria

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

Inclusion Criteria:

  1. Age greater than 18 years.
  2. Being able to understand the explanations about the potential benefits and risks of study participation.
  3. Diagnosis of chronic plantar fasciitis. Proven by clinical examination: Meeting at least 2 of the following criteria:

    • Tenderness in the proximal insertion of the plantar fascia (area of the medial calcaneal tuberosity).
    • Pain during the first steps to get out of bed in the morning and / or after a period of rest time.
  4. With a duration of symptoms ≥ 6 months at the time of study entry.
  5. Having received conservative therapy without success, at least two treatments. Treatments may have been made isolated, combined or consecutively.

Exclusion Criteria:

  1. Bilateral plantar fasciitis.
  2. Hiper/ hypothyroidism.
  3. Diabetes mellitus.
  4. Treatment with anticoagulants
  5. Inflammatory diseases.

Sites / Locations

  • Rehabilitation Center "Salut i Esport"

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Standard shock waves device

Austere shock waves device

Sophisticated shock waves device

Arm Description

3 sessions were applied: one per week.

3 sessions were applied: one per week.

3 sessions were applied: one per week.

Outcomes

Primary Outcome Measures

Function of the foot
FFI (Foot Function Index) questionnaire

Secondary Outcome Measures

Pain
VAS (Visual Analogical Scale)
Plantar fascia thickness
Ultrasounds
Perception of patient recovery
Likert scale
Painkillers consumption
Painkillers consumption
Adverse effects
Adverse effects

Full Information

First Posted
November 13, 2015
Last Updated
November 17, 2015
Sponsor
Asociacion Colaboracion Cochrane Iberoamericana
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1. Study Identification

Unique Protocol Identification Number
NCT02608723
Brief Title
Shock Wave Therapy: Do the External Appearance of the Device Influence Clinical Outcomes?
Official Title
Chronic Plantar Fasciitis Treated With Shock Wave Therapy: Do the External Appearance of the Device Influence Clinical Outcomes? A Randomized Controlled Clinical Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
June 2014 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Asociacion Colaboracion Cochrane Iberoamericana

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To check in patients suffering from chronic plantar fasciitis treated with shock wave therapy, if the outward appearance of the device affects clinical outcomes.
Detailed Description
Study Design: a controlled, randomized, parallel assessor-blinded clinical trial. Patients suffering from chronic plantar fasciitis (duration more than 6 months) will be assigned to three different groups: Group I: Treatment applied by standard shock waves device. Group II: Shock wave therapy applied by a modified standard device to offer more attractive, more technical, smarter, better appearance, larger and with an expansion of external information devices more sophisticated. Group III: Shock wave therapy applied by a modified standard device to offer a more austere, disfigured, unattractive, modest and smaller external appearance. The shock waves emitted to the 3 devices will be identical; the only difference will be the external image of the device. The main outcome will be the function of the foot by the FFI (Foot Function Index) questionnaire. As secondary variables: pain by VAS (Visual Analogical Scale) in different situations, the plantar fascia thickness measured by ultrasound, and the perception of patient recovery measured with the Likert scale. Adverse effects, painkillers consumption and pain experienced during the treatment of shock waves were also assessed. The patients will be followed and monitored for a month, two months and four months after treatment finished. For the statistical analysis of clinical variables, ANOVA (analysis of variance) will be performed to check whether the evolution of patients over time was different depending on the device applied.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Plantar Fasciitis, Pain
Keywords
shock wave, plantar fasciitis, placebo effect, nocebo effect

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
135 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard shock waves device
Arm Type
Active Comparator
Arm Description
3 sessions were applied: one per week.
Arm Title
Austere shock waves device
Arm Type
Active Comparator
Arm Description
3 sessions were applied: one per week.
Arm Title
Sophisticated shock waves device
Arm Type
Active Comparator
Arm Description
3 sessions were applied: one per week.
Intervention Type
Device
Intervention Name(s)
Standard shock waves device
Intervention Description
3 sessions were applied: one per week. Energy flux density 0,18 mJ/mm2. Frequency: 8 Hz. 2500 shockwaves/session. The shock waves emitted to the 3 devices are identical; the only difference is the external image of the device.
Intervention Type
Device
Intervention Name(s)
Austere shock waves device
Intervention Description
3 sessions were applied: one per week. Energy flux density 0,18 mJ/mm2. Frequency: 8 Hz. 2500 shockwaves/session. The shock waves emitted to the 3 devices are identical; the only difference is the external image of the device.
Intervention Type
Device
Intervention Name(s)
Sophisticated shock waves device
Intervention Description
3 sessions were applied: one per week. Energy flux density 0,18 mJ/mm2. Frequency: 8 Hz. 2500 shockwaves/session. The shock waves emitted to the 3 devices are identical; the only difference is the external image of the device.
Primary Outcome Measure Information:
Title
Function of the foot
Description
FFI (Foot Function Index) questionnaire
Time Frame
Four months
Secondary Outcome Measure Information:
Title
Pain
Description
VAS (Visual Analogical Scale)
Time Frame
Four months
Title
Plantar fascia thickness
Description
Ultrasounds
Time Frame
Four months
Title
Perception of patient recovery
Description
Likert scale
Time Frame
Four months
Title
Painkillers consumption
Description
Painkillers consumption
Time Frame
Four months
Title
Adverse effects
Description
Adverse effects
Time Frame
Four months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age greater than 18 years. Being able to understand the explanations about the potential benefits and risks of study participation. Diagnosis of chronic plantar fasciitis. Proven by clinical examination: Meeting at least 2 of the following criteria: Tenderness in the proximal insertion of the plantar fascia (area of the medial calcaneal tuberosity). Pain during the first steps to get out of bed in the morning and / or after a period of rest time. With a duration of symptoms ≥ 6 months at the time of study entry. Having received conservative therapy without success, at least two treatments. Treatments may have been made isolated, combined or consecutively. Exclusion Criteria: Bilateral plantar fasciitis. Hiper/ hypothyroidism. Diabetes mellitus. Treatment with anticoagulants Inflammatory diseases.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antoni Morral, PhDc
Organizational Affiliation
Rehabilitation Center "Salut i Esport"
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rehabilitation Center "Salut i Esport"
City
Santa Perpetua
State/Province
Barcelona
ZIP/Postal Code
08130
Country
Spain

12. IPD Sharing Statement

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Shock Wave Therapy: Do the External Appearance of the Device Influence Clinical Outcomes?

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