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The CurePPaC Study - Analysing Non-surgical Treatment Strategies to Cure Pes Planovalgus Associated Complaints

Primary Purpose

Foot Injuries, Posterior Tibial Tendon Dysfunction

Status
Terminated
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Foot Orthoses Only
Foot Orthoses and Eccentric Exercise
Sham Foot Orthoses
Sponsored by
Bern University of Applied Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Foot Injuries focused on measuring conservative therapy, Foot-Function-Index, functional movement changes, non-surgical treatment, pes planovalgus, posterior tibial tendon dysfunction

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 18-60
  • Current complaint of foot and ankle pain that lasted for 3 months or more
  • Flexible Pes planovalgus deformity in the clinical assessment
  • Posterior tibial tendon dysfunction (PTTD) of stage I and II (Johnson & Strom 1989)
  • Pes planovalgus foot deformity with longitudinal arch flattening verified by radiograph (Younger 2005): Lateral view: lateral talo-first metatarsal angle ≠ 0° (break of axis): angle >10° according to Younger (2005); 60Anteroposterior view: anteroposterior talo-first metatarsal angle ≠ 0° (break of axis): angle >10° according to Younger (2005)
  • "too-many toes"-sign from rear frontal view with an abducted forefoot (Johnson & Strom 1989, Kulig 2009b)
  • Eligibility for non-surgical treatment
  • No indication / not yet an indication for surgical treatment of foot deformity

Exclusion Criteria:

  • Rigid foot deformity
  • Posterior tibial tendon dysfunction (PTTD) of stage III and IV according to Johnson & Strom 1989 (=>rigid foot deformity)
  • Cardio-, neuro-, or peripheral vascular pathology, musculoskeletal pathology, acute infection or alcohol addiction limiting participation in study protocol
  • Acute use of local or systemic analgesics
  • Acute physical therapy, training therapy or physiotherapy
  • Acute overuse or traumatic injury to the lower leg (excluding Pes planovalgus associated pathology)
  • Prior surgery to the lower limb

Sites / Locations

  • Spital Netz Bern Ziegler
  • Klinik Sonnenhof Bern
  • Inselspital, University Hospital Bern
  • Salem Spital Bern
  • Salem-Spital Orthopädische Klinik Bern
  • spital STS AG

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Sham Comparator

Arm Label

Foot Orthoses Only

Foot Orthoses and Eccentric Exercise

Sham Foot Orthoses

Arm Description

including Patient Education; Abbreviation: FOO

including Patient Education; Abbreviation: FOE

including Patient Education; Abbreviation: FOS

Outcomes

Primary Outcome Measures

Foot Function Index - total score
additional analysis of change from baseline to week 4, and analysis of change from baseline to week 8

Secondary Outcome Measures

Foot Function Index - subcategory pain
additional analysis of change from baseline to week 4, and analysis of change from baseline to week 8
Foot Function Index - subcategory disability
additional analysis of change from baseline to week 4, and analysis of change from baseline to week 8
Foot Function Index - subcategory activity limitation
additional analysis of change from baseline to week 4, and analysis of change from baseline to week 8

Full Information

First Posted
April 17, 2013
Last Updated
October 25, 2017
Sponsor
Bern University of Applied Sciences
Collaborators
Swiss National Science Foundation, Insel Gruppe AG, University Hospital Bern
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1. Study Identification

Unique Protocol Identification Number
NCT01839669
Brief Title
The CurePPaC Study - Analysing Non-surgical Treatment Strategies to Cure Pes Planovalgus Associated Complaints
Official Title
The CurePPaC Study - Analysing Non-surgical Treatment Strategies to Cure Pes Planovalgus Associated Complaints
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Terminated
Why Stopped
Not possible to enroll enough patients in reasonable time.
Study Start Date
July 2013 (undefined)
Primary Completion Date
October 25, 2017 (Actual)
Study Completion Date
October 25, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bern University of Applied Sciences
Collaborators
Swiss National Science Foundation, Insel Gruppe AG, University Hospital Bern

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Pes planovalgus, also called flat foot, is a common foot deformity characterized by a flattening of the foot's longitudinal arch and is accompanied by a dysfunction of the posterior tibial tendon ("posterior tibial tendon dysfunction" or "PTTD"). Early stages of this pathology are thought to be treated with non-surgical therapy options like foot orthoses (relief of tendon stress by mechanical unloading of the arch), strengthening exercises or basic physiotherapeutic measures. Recent literature clearly states the urgent need for high quality studies to evaluate the proposed non-surgical treatments (Bowring 2009, 2010). There is only one high quality study available that shows benefits of orthoses therapy and exercise (Kulig 2009). No study to date evaluated functional changes pre-post in dynamic movement pattern like gait or stair climbing. The widespread use of several non-surgical treatment strategies lead to extensive financial expenses of the health care system. An optimized therapeutic strategy could eventually lead to more efficient health care investments. The presented proposal addresses this latest knowledge and aims to analyse non-surgical treatment strategies to Cure Pes Planovalgus associated Complaints (CurePPaC) in the CurePPaC Study.
Detailed Description
Introduction: Pes planovalgus or flatfoot-associated complaints are frequent symptoms, which are thought to be caused by the foot deformity itself. Concurrently, the multifactorial weakness of the M. tibialis posterior and its tendon (trauma, systemic disease, chronic tendon degeneration by overuse) can lead to a flattening of the medial longitudinal arch of the foot. Affected patients suffer from functional impairment and pain. Less severe cases are eligible for non-surgical treatment. Foot orthoses are considered to be the first line approach. Furthermore strengthening of the arch and ankle stabilizing muscles are thought to contribute to an active compensation of the deformity. There is only limited evidence concerning the numerous therapy approaches since high quality studies are missing. One excellent report (Kulig et al. 2009) shows clear benefits by the use of foot orthoses and eccentric strengthening exercises. Beside the fact that evidence-based guidelines for therapy have yet to be developed, no data is available showing functional benefits that accompany the therapy process. This would give further insight into mechanisms behind non-surgical management strategies and how patients benefit functionally from therapy. Purpose: The purpose of this randomized longitudinal intervention study is the evaluation of the therapeutic benefit of three different non-surgical treatment regimens (foot orthoses only FOO, foot orthoses and eccentric exercise FOE, foot orthoses sham treatment FOS) in patients with Pes planovalgus and accompanying complaints. Furthermore the analysis of possible functional changes in gait mechanics (kinematic and kinetic view) and neuromuscular control (electromyographic analysis) will contribute to a superior understanding of functional changes that accompany non-operative management. The purpose of the study is to optimize non-surgical management in patients suffering from Pes planovalgus associated pain leading to an efficient use of health care system's financial resources. Methods: 60 patients with Pes planovalgus associated complaints (clinical diagnosis with plain weight bearing radiographs), M. tibialis posterior dysfunction) are included in the study. Functional impairment is evaluated pre and post intervention by the Foot-Function-Index (FFI, German version). Anthropometric data recording is followed by preparation of subject's foot anatomical landmarks with retroreflective markers and superficially detectable muscles of the ankle joint complex are prepared with surface electromyography (SEMG) electrodes. The 3D kinematic data allows inter alia the calculation of segmental angels of the lower extremity and measurement of navicular drop. The neuromuscular activity is analysed in the time (on-off pattern) and amplitude domain (gait cycle specific phases). Procedure: Potential participants are recruited via the Outpatient Clinic of the Department of Orthopaedic Surgery of the Inselspital, University Hospital, Bern. After initial screening, subjects are randomized to one of three intervention groups (foot orthoses only FOO, foot orthoses and eccentric exercise FOE, foot orthoses sham treatment FOS). FOO-subjects wear custom-made foot orthoses only. FOE-subjects wear individually accustomed foot orthoses and they will perform a combined monitored and home training program to progressively strengthen the M. tibialis posterior and accompanying ankle stabilizing muscles with eccentric exercises. FOS-subjects wear custom-made sham foot orthoses without the functional elements of the treatment orthoses (longitudinal arch support, ankle stabilizer, bowl-shaped heel for rearfoot stability). Subjects are measured pre and post intervention (12 weeks). Measurements include the primary outcome measure Foot-Function-Index (FFI, German version: total score) followed by basic anthropometric measures. Subject preparation allows then the measurement of 10 trials on a walkway and on stairs with embedded force plates in barefoot condition. An average step cycle out of 10 trials is calculated and biomechanical outcome measures are extracted. A re-test allows the calculation of intervention effects by one-factor ANOVA (group: treatment FOO vs. FOE vs. FOS) for repeated measures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Foot Injuries, Posterior Tibial Tendon Dysfunction
Keywords
conservative therapy, Foot-Function-Index, functional movement changes, non-surgical treatment, pes planovalgus, posterior tibial tendon dysfunction

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Foot Orthoses Only
Arm Type
Active Comparator
Arm Description
including Patient Education; Abbreviation: FOO
Arm Title
Foot Orthoses and Eccentric Exercise
Arm Type
Experimental
Arm Description
including Patient Education; Abbreviation: FOE
Arm Title
Sham Foot Orthoses
Arm Type
Sham Comparator
Arm Description
including Patient Education; Abbreviation: FOS
Intervention Type
Device
Intervention Name(s)
Foot Orthoses Only
Intervention Description
patients wear foot orthoses as a treatment condition - no further therapy
Intervention Type
Procedure
Intervention Name(s)
Foot Orthoses and Eccentric Exercise
Intervention Description
patients wear foot orthoses and they perform an additional home-based eccentric training program for the M. tibialis posterior
Intervention Type
Device
Intervention Name(s)
Sham Foot Orthoses
Intervention Description
patient wear sham foot orthoses (control condition)
Primary Outcome Measure Information:
Title
Foot Function Index - total score
Description
additional analysis of change from baseline to week 4, and analysis of change from baseline to week 8
Time Frame
change from baseline (pre intervention) to week 12 (post intervention)
Secondary Outcome Measure Information:
Title
Foot Function Index - subcategory pain
Description
additional analysis of change from baseline to week 4, and analysis of change from baseline to week 8
Time Frame
change from baseline (pre intervention) to week 12 (post intervention)
Title
Foot Function Index - subcategory disability
Description
additional analysis of change from baseline to week 4, and analysis of change from baseline to week 8
Time Frame
change from baseline (pre intervention) to week 12 (post intervention)
Title
Foot Function Index - subcategory activity limitation
Description
additional analysis of change from baseline to week 4, and analysis of change from baseline to week 8
Time Frame
change from baseline (pre intervention) to week 12 (post intervention)
Other Pre-specified Outcome Measures:
Title
Pain Disability Index
Description
additional analysis of change from baseline to week 4, and analysis of change from baseline to week 8
Time Frame
change from baseline (pre intervention) to week 12 (post intervention)
Title
Visual Analogue Scale
Description
assessing pain pre- and post biomechanical testing / change from baseline to week 12
Time Frame
change from baseline (pre intervention) to week 12 (post intervention)
Title
kinematic data from 3d movement analysis
Description
regarding distance: navicular drop; regarding angular data (angle at initial contact, max. manifestation during stance, range): foot progression angle, forefoot to rearfoot dorsiflexion, forefoot to rearfoot adduction, forefoot to rearfoot supination, ankle dorsiflexion, ankle adduction, ankle eversion, knee flexion, knee adduction, knee internal rotation, hip flexion, hip adduction, hip internal rotation
Time Frame
change from baseline (pre intervention) to week 12 (post intervention)
Title
neuromuscular activity
Description
EMG of M. tibialis anterior, M. peroneus longus, M. gastrocnemius lateralis/medialis, M. soleus: onset of activation, time of maximum activation, total time of activation, normalized amplitude in preactivation, normalized amplitude in weight acceptance, normalized amplitude in mid-stance, normalized amplitude in push-off
Time Frame
change from baseline (pre intervention) to week 12 (post intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 18-60 Current complaint of foot and ankle pain that lasted for 3 months or more Flexible Pes planovalgus deformity in the clinical assessment Posterior tibial tendon dysfunction (PTTD) of stage I and II (Johnson & Strom 1989) Pes planovalgus foot deformity with longitudinal arch flattening verified by radiograph (Younger 2005): Lateral view: lateral talo-first metatarsal angle ≠ 0° (break of axis): angle >10° according to Younger (2005); 60Anteroposterior view: anteroposterior talo-first metatarsal angle ≠ 0° (break of axis): angle >10° according to Younger (2005) "too-many toes"-sign from rear frontal view with an abducted forefoot (Johnson & Strom 1989, Kulig 2009b) Eligibility for non-surgical treatment No indication / not yet an indication for surgical treatment of foot deformity Exclusion Criteria: Rigid foot deformity Posterior tibial tendon dysfunction (PTTD) of stage III and IV according to Johnson & Strom 1989 (=>rigid foot deformity) Cardio-, neuro-, or peripheral vascular pathology, musculoskeletal pathology, acute infection or alcohol addiction limiting participation in study protocol Acute use of local or systemic analgesics Acute physical therapy, training therapy or physiotherapy Acute overuse or traumatic injury to the lower leg (excluding Pes planovalgus associated pathology) Prior surgery to the lower limb
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heiner Baur, PhD
Organizational Affiliation
Bern University of Applied Sciences, Switzerland
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Heiner Baur, PhD
Organizational Affiliation
Bern University of Applied Sciences, Health, aR&D Physiotherapy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Spital Netz Bern Ziegler
City
Bern
ZIP/Postal Code
3001
Country
Switzerland
Facility Name
Klinik Sonnenhof Bern
City
Bern
ZIP/Postal Code
3006
Country
Switzerland
Facility Name
Inselspital, University Hospital Bern
City
Bern
ZIP/Postal Code
3012
Country
Switzerland
Facility Name
Salem Spital Bern
City
Bern
ZIP/Postal Code
3013
Country
Switzerland
Facility Name
Salem-Spital Orthopädische Klinik Bern
City
Bern
ZIP/Postal Code
3013
Country
Switzerland
Facility Name
spital STS AG
City
Thun
ZIP/Postal Code
3600
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
16221454
Citation
Younger AS, Sawatzky B, Dryden P. Radiographic assessment of adult flatfoot. Foot Ankle Int. 2005 Oct;26(10):820-5. doi: 10.1177/107110070502601006.
Results Reference
background
PubMed Identifier
2912622
Citation
Johnson KA, Strom DE. Tibialis posterior tendon dysfunction. Clin Orthop Relat Res. 1989 Feb;(239):196-206.
Results Reference
background
PubMed Identifier
19022863
Citation
Kulig K, Reischl SF, Pomrantz AB, Burnfield JM, Mais-Requejo S, Thordarson DB, Smith RW. Nonsurgical management of posterior tibial tendon dysfunction with orthoses and resistive exercise: a randomized controlled trial. Phys Ther. 2009 Jan;89(1):26-37. doi: 10.2522/ptj.20070242. Epub 2008 Nov 20.
Results Reference
background
PubMed Identifier
20434675
Citation
Bowring B, Chockalingam N. Conservative treatment of tibialis posterior tendon dysfunction--a review. Foot (Edinb). 2010 Mar;20(1):18-26. doi: 10.1016/j.foot.2009.11.001. Epub 2009 Dec 24.
Results Reference
background
PubMed Identifier
20307479
Citation
Bowring B, Chockalingam N. A clinical guideline for the conservative management of tibialis posterior tendon dysfunction. Foot (Edinb). 2009 Dec;19(4):211-7. doi: 10.1016/j.foot.2009.08.001. Epub 2009 Sep 18.
Results Reference
background
PubMed Identifier
26279682
Citation
Blasimann A, Eichelberger P, Brulhart Y, El-Masri I, Fluckiger G, Frauchiger L, Huber M, Weber M, Krause FG, Baur H. Non-surgical treatment of pain associated with posterior tibial tendon dysfunction: study protocol for a randomised clinical trial. J Foot Ankle Res. 2015 Aug 14;8:37. doi: 10.1186/s13047-015-0095-4. eCollection 2015.
Results Reference
background
Links:
URL
http://p3.snf.ch/project-140928
Description
project description in the database of the Swiss National Science Foundation

Learn more about this trial

The CurePPaC Study - Analysing Non-surgical Treatment Strategies to Cure Pes Planovalgus Associated Complaints

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