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Surgical or Non-surgical Treatment of Plantar Fasciitis (SOFT)

Primary Purpose

Fasciitis, Plantar, Chronic

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Radiofrequency microtenotomy
Strength training
Sponsored by
University of Southern Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fasciitis, Plantar, Chronic

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • VAS pain score > 30 within last 7 days
  • Plantar heel pain> 7 months
  • Palpation soreness fascia plantaris at heel
  • Plantar heel pain during first steps (First-step sign)
  • Read and understand Danish

Exclusion Criteria:

  • Systemic diseases or neuropathy
  • Diabetes
  • Pregnant
  • Previous heel surgery on same foot
  • Cortisone injections within past 3 months
  • Bilateral symptom onset within past 7 days
  • Signs of tarsal tunnel
  • Facia plantaris thickness of less than 4 mm
  • Performed message / head recovery / stretching within the past month
  • Any treatment for plantar pain within the past 3 months
  • Other reasons

Sites / Locations

  • Lillebaelt Hospital, KoldingRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Surgical

Non-surgical

Arm Description

Radiofrequency microtenotomy (RF): A longitudinal incision of about 3 cm will be made over the most tender part of the foot taking care to avoid the weight bearing part of the sole, and the tissues dissected down to the affected plantar fascia. After initiating sterile isotonic saline flow of 1 drop every 1-2 s from a line connected to the RF system, the TOPAZ tip will be placed onto the fascia and the micro debridements carried out in a grid like pattern on and throughout the symptomatic fascia area. After debridement, the wound will be irrigated with copious amounts of normal saline solution and closed in layers. A local anaesthetic will be injected into the skin and subcutaneous tissues around the wound and standard wound dressings will be applied

Strength training: Consists of one-legged heel lift to primarily activate the windlass effect and increase the mechanical stress on the tendon. The exercise is performed on a step, a thick book or the like, so the heel movement finishes below the horizontal level. The exercise is performed every other day with as many sets as possible and as heavy as possible, but not heavier than eight repetitions can be performed per. set. The load progressed from two to one leg +/- backpack. The exercise is performed as 3 s/2 s / 3 s concentric, isometric and eccentric respectively followed by 2 min rest. Patients continue to exercise 4 weeks after patient acceptable symptom state (PASS) has been achieved

Outcomes

Primary Outcome Measures

Change in the Foot Health Status Questionnaire (FHSQ)
Subdomain foot pain score range 0-100, low values represent worse conditions

Secondary Outcome Measures

The Foot Health Status Questionnaire (FHSQ)
Subdomains (foot related function, footwear and general foot health perception). Subdomain scores range from 0-100, low scores represent worse conditions
Visual Analog Scale (VAS)
Pain and scores range from 0-100, low values represent worse conditions
Global Percieved Effect (GPE)
A questionnaire using a 7-point likert scale to asses change in symptoms. The scores are categorized into (1-2 = deterioration of symptoms, 3-5 = Neutral, 6-7 improvement of symptoms).
Physical Activity Questionnaire (IPAQ)
Participation in sports and activities of daily living measured as MET-minutes/day or MET-minutes/week. Low MET-scores indicate limited activity. MET = metabolic equivalent of task

Full Information

First Posted
February 8, 2019
Last Updated
May 17, 2022
Sponsor
University of Southern Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT03854682
Brief Title
Surgical or Non-surgical Treatment of Plantar Fasciitis
Acronym
SOFT
Official Title
Surgical or Non-surgical Treatment of Plantar Fasciitis - A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2020 (Actual)
Primary Completion Date
June 1, 2024 (Anticipated)
Study Completion Date
June 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern Denmark

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Plantar fasciitis (PF) is one of the most common causes of heel pain in 40-60 year old people. Approximately 10% of the population is affected by the disorder and the PF prevalence is 3.6-7.0%. The risk factors include decreased ankle dorsiflexion, overweight (BMI> 27), pronated foot position, and prolonged work and activity-related weight bearing. The condition affects both active and less active people. The typical symptoms are pain around the attachment of the foot's tendon mirror (fascia plantaris), especially the medial part. The pain is well defined and occurs during weight bearing activities or during the first steps after rest. The walking pattern is changed to relieve pain. Ultrasound scan is used to confirm the diagnosis (thickened tendon mirror> 4 mm). The condition is described as inflammatory, but the relationship between the initial inflammatory condition and the chronic tendon mirror overload injury (fasciopathy) is unknown and marked by degenerative changes. Although the majority of people improve within 1-2 years, the long-term prognosis is unknown. People with symptoms lasting > 7 months have poor prognosis and should be offered other treatment. Non-surgical treatment is often first line of treatment followed by surgical treatment. In this clinical trial investigators compare pain levels (FHSQ-DK) in people, who receive surgical treatment (radiofrequency microtenotomy, shoe inserts and patient education) and people who receive non-surgical treatment (strength training, shoe inserts and patient education) with a primary end-point at 6 months. The hypothesis is that surgical treatment is better than non-surgical treatment measured by FHSQ-DK (pain)
Detailed Description
To be completed later

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A prospective, blinded, parallel-group trial with balanced randomization [1:1], in accordance with CONSORT
Masking
InvestigatorOutcomes Assessor
Masking Description
Blinding to treatment allocation of patients, physiotherapists (health care providers) will not be possible due to the nature of the interventions. However, independent data collectors will be responsible for baseline and follow-up assessments, while all self-reported outcome measures will be made available to the patients electronically, and responses entered into a database identified by identification numbers only. The data analyst will be unaware of the treatment allocation as data will be analyzed using recoded identification numbers. The recoding will be performed by an independent person.
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Surgical
Arm Type
Experimental
Arm Description
Radiofrequency microtenotomy (RF): A longitudinal incision of about 3 cm will be made over the most tender part of the foot taking care to avoid the weight bearing part of the sole, and the tissues dissected down to the affected plantar fascia. After initiating sterile isotonic saline flow of 1 drop every 1-2 s from a line connected to the RF system, the TOPAZ tip will be placed onto the fascia and the micro debridements carried out in a grid like pattern on and throughout the symptomatic fascia area. After debridement, the wound will be irrigated with copious amounts of normal saline solution and closed in layers. A local anaesthetic will be injected into the skin and subcutaneous tissues around the wound and standard wound dressings will be applied
Arm Title
Non-surgical
Arm Type
Active Comparator
Arm Description
Strength training: Consists of one-legged heel lift to primarily activate the windlass effect and increase the mechanical stress on the tendon. The exercise is performed on a step, a thick book or the like, so the heel movement finishes below the horizontal level. The exercise is performed every other day with as many sets as possible and as heavy as possible, but not heavier than eight repetitions can be performed per. set. The load progressed from two to one leg +/- backpack. The exercise is performed as 3 s/2 s / 3 s concentric, isometric and eccentric respectively followed by 2 min rest. Patients continue to exercise 4 weeks after patient acceptable symptom state (PASS) has been achieved
Intervention Type
Procedure
Intervention Name(s)
Radiofrequency microtenotomy
Intervention Description
A longitudinal incision of about 3 cm will be made over the most tender part of the foot taking care to avoid the weight bearing part of the sole, and the tissues dissected down to the affected plantar fascia. After initiating sterile isotonic saline flow of 1 drop every 1-2 s from a line connected to the RF system, the TOPAZ tip will be placed onto the fascia and the micro debridements carried out in a grid like pattern on and throughout the symptomatic fascia area. After debridement, the wound will be irrigated with copious amounts of normal saline solution and closed in layers. A local anaesthetic will be injected into the skin and subcutaneous tissues around the wound and standard wound dressings will be applied
Intervention Type
Behavioral
Intervention Name(s)
Strength training
Other Intervention Name(s)
Resistance training
Intervention Description
Non-surgical treatment consists of one-legged heel lift to primarily activate the windlass effect and increase the mechanical stress on the tendon. The exercise is performed on a step, a thick book or the like, so the heel movement finishes below the horizontal level. The exercise is performed every other day with as many sets as possible and as heavy as possible, but not heavier than eight repetitions can be performed per. set. The load progressed from two to one leg +/- backpack. The exercise is performed as 3 s/2 s / 3 s concentric, isometric and eccentric respectively followed by 2 min rest. Patients continue to exercise 4 weeks after patient acceptable symptom state (PASS) has been achieved
Primary Outcome Measure Information:
Title
Change in the Foot Health Status Questionnaire (FHSQ)
Description
Subdomain foot pain score range 0-100, low values represent worse conditions
Time Frame
Change from baseline at 6 months
Secondary Outcome Measure Information:
Title
The Foot Health Status Questionnaire (FHSQ)
Description
Subdomains (foot related function, footwear and general foot health perception). Subdomain scores range from 0-100, low scores represent worse conditions
Time Frame
Change from baseline at 6 months
Title
Visual Analog Scale (VAS)
Description
Pain and scores range from 0-100, low values represent worse conditions
Time Frame
Change from baseline at 6 months
Title
Global Percieved Effect (GPE)
Description
A questionnaire using a 7-point likert scale to asses change in symptoms. The scores are categorized into (1-2 = deterioration of symptoms, 3-5 = Neutral, 6-7 improvement of symptoms).
Time Frame
1,3,6,12 months post-intervention
Title
Physical Activity Questionnaire (IPAQ)
Description
Participation in sports and activities of daily living measured as MET-minutes/day or MET-minutes/week. Low MET-scores indicate limited activity. MET = metabolic equivalent of task
Time Frame
Change from baseline at 6 months
Other Pre-specified Outcome Measures:
Title
Compliance with the prescribed intervention
Description
Tracking adherence to exercise and reasons for non-complience
Time Frame
6 months
Title
Complications and side-effects
Description
Review of medical records for complications and side-effects
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: VAS pain score > 30 within last 7 days Plantar heel pain> 7 months Palpation soreness fascia plantaris at heel Plantar heel pain during first steps (First-step sign) Read and understand Danish Exclusion Criteria: Systemic diseases or neuropathy Diabetes Pregnant Previous heel surgery on same foot Cortisone injections within past 3 months Bilateral symptom onset within past 7 days Signs of tarsal tunnel Facia plantaris thickness of less than 4 mm Performed message / head recovery / stretching within the past month Any treatment for plantar pain within the past 3 months Other reasons
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jens Wester, MD
Phone
+45 76362333
Email
Jens.Wester1@rsyd.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Bjarke Viberg, MD
Phone
+45 76362333
Email
bjarke.viberg@rsyd.dk
Facility Information:
Facility Name
Lillebaelt Hospital, Kolding
City
Kolding
ZIP/Postal Code
6000
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jens Wester, MD
Email
jens.wester1@rsyd.dk
First Name & Middle Initial & Last Name & Degree
Anne Hansen
Email
Anne.Jess.Hansen@rsyd.dk

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36195936
Citation
Moller S, Riel H, Wester J, Simony A, Viberg B, Jensen C. Surgical or non-surgical treatment of plantar fasciopathy (SOFT): study protocol for a randomized controlled trial. Trials. 2022 Oct 4;23(1):845. doi: 10.1186/s13063-022-06785-w.
Results Reference
derived

Learn more about this trial

Surgical or Non-surgical Treatment of Plantar Fasciitis

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