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WBV and Acute Lateral Ankle Sprain (WBV and ALAS)

Primary Purpose

Postural Control, Subjective Instablity

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Whole body vibration (Galileo® Med M Plus, Novotec, Pforzheim, Germany)
Physiotherapy
Sponsored by
Ludwig-Maximilians - University of Munich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postural Control

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Acute, unilateral, unstable, inversion ankle sprain (Grade II, III)

Exclusion Criteria:

  • Pregnancy
  • Conditions affecting the neuromuscular- or musculoskeletal System
  • Previous surgical interventions to the foot, ankle, knee or hip; known FAI, CAI
  • Conditions possibly affecting balance
  • Cardiovascular disease including thrombosis
  • Respiratory diseases
  • Abdominal diseases (including gallstones)
  • Urological diseases (including kidney- and bladder stones)
  • Gynaecological diseases and + intrauterine devices
  • Neurological diseases including epilepsia within the last 2 years
  • Acute injuries to the head
  • Patient is not available for follow up visits
  • Patient unable to give informed consent
  • Patient suspected to be non-compliant

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    WBV

    Physiotherapy

    Arm Description

    Patients will receive supervised physical therapy using a whole body vibration device (Galileo® Med M Plus, Novotec, Pforzheim, Germany) twice a week, 30 minutes per session, for 6 weeks.

    Patient will receive the current gold standard treatment protocol: supervised physical therapy, twice a week, 30 minutes per session, for 6 weeks.

    Outcomes

    Primary Outcome Measures

    Postural control
    Sway Index measured via the Leonardo Mechanograph GRFP (16 bit, 800 Hz; NOVOTEC Medical GmbH, Germany)

    Secondary Outcome Measures

    Subjective instability
    Patient recorded giving-way symptoms or recurrence

    Full Information

    First Posted
    October 3, 2012
    Last Updated
    October 4, 2012
    Sponsor
    Ludwig-Maximilians - University of Munich
    Collaborators
    Medical University Innsbruck
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01702597
    Brief Title
    WBV and Acute Lateral Ankle Sprain
    Acronym
    WBV and ALAS
    Official Title
    The Effect of Whole Body Vibration and Acute Unilateral Unstable Lateral Ankle Sprain - A Biphasic Randomized Controlled Trial -
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2012
    Overall Recruitment Status
    Unknown status
    Study Start Date
    October 2012 (undefined)
    Primary Completion Date
    April 2013 (Anticipated)
    Study Completion Date
    April 2014 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Ludwig-Maximilians - University of Munich
    Collaborators
    Medical University Innsbruck

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The aim of this bicentric, biphasic, randomized, controlled study is to compare of the current gold standard functional treatment to functional treatment plus WBV in patients with acute unilateral unstable inversion ankle sprains over a period of 12 months
    Detailed Description
    Background: Ankle sprains often result in ankle instability, which is most likely caused by damage to passive and neurological structures. Whole body vibration (WBV) is a neuromuscular training method improving those neurologic parameters impaired. The aim of this study is to compare the current gold standard functional treatment to functional treatment plus WBV in patients with acute unilateral unstable inversion ankle sprains. Methods/Design: 60 patients, aged 18-40 years, presenting with an isolated, unilateral, acute unstable inversion ankle sprain will be included in this bicentric, biphasic, randomized controlled trial. Patients will be randomized by envelope drawing. All patients will be allowed early mobilization and pain-depending weight bearing, limited functional immobilization by orthesis, PRICE, NSARDs as well as home and supervised physiotherapy. Supervised physical therapy will take place twice a week, 30 minutes per session, for 6 weeks, following a standardized intervention protocol. During supervised physical therapy, the intervention group will perform similar exercises on a side-alternating sinusoidal vibration platform as the control group. Two time dependent primary outcome parameters will be assessed. Short-term outcome after six weeks will be postural control quantified by the sway index. Mid-term outcome after one year will be assessed by subjective instability, defined by the presence of giving-way attacks. Secondary outcome parameters include return to pre-injury level of activities, residual pain, recurrence, objective instability, energy / coordination, Foot and Ankle Disability Index and EQ 5D.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Postural Control, Subjective Instablity

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    WBV
    Arm Type
    Experimental
    Arm Description
    Patients will receive supervised physical therapy using a whole body vibration device (Galileo® Med M Plus, Novotec, Pforzheim, Germany) twice a week, 30 minutes per session, for 6 weeks.
    Arm Title
    Physiotherapy
    Arm Type
    Active Comparator
    Arm Description
    Patient will receive the current gold standard treatment protocol: supervised physical therapy, twice a week, 30 minutes per session, for 6 weeks.
    Intervention Type
    Device
    Intervention Name(s)
    Whole body vibration (Galileo® Med M Plus, Novotec, Pforzheim, Germany)
    Other Intervention Name(s)
    WBV, Galileo
    Intervention Description
    Patients will train on a WBV platform, following a standardized protocol, aiming at improving strength, endurance and proprioception of both legs.
    Intervention Type
    Other
    Intervention Name(s)
    Physiotherapy
    Other Intervention Name(s)
    Physical Therapy, Training
    Intervention Description
    Patients will receive a standardized physical therapy.
    Primary Outcome Measure Information:
    Title
    Postural control
    Description
    Sway Index measured via the Leonardo Mechanograph GRFP (16 bit, 800 Hz; NOVOTEC Medical GmbH, Germany)
    Time Frame
    6 weeks
    Secondary Outcome Measure Information:
    Title
    Subjective instability
    Description
    Patient recorded giving-way symptoms or recurrence
    Time Frame
    1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Acute, unilateral, unstable, inversion ankle sprain (Grade II, III) Exclusion Criteria: Pregnancy Conditions affecting the neuromuscular- or musculoskeletal System Previous surgical interventions to the foot, ankle, knee or hip; known FAI, CAI Conditions possibly affecting balance Cardiovascular disease including thrombosis Respiratory diseases Abdominal diseases (including gallstones) Urological diseases (including kidney- and bladder stones) Gynaecological diseases and + intrauterine devices Neurological diseases including epilepsia within the last 2 years Acute injuries to the head Patient is not available for follow up visits Patient unable to give informed consent Patient suspected to be non-compliant
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Matthias Schieker, Prof.
    Organizational Affiliation
    Ludwig-Maximilians - University of Munich
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    23316791
    Citation
    Baumbach SF, Fasser M, Polzer H, Sieb M, Regauer M, Mutschler W, Schieker M, Blauth M. Study protocol: the effect of whole body vibration on acute unilateral unstable lateral ankle sprain- a biphasic randomized controlled trial. BMC Musculoskelet Disord. 2013 Jan 14;14:22. doi: 10.1186/1471-2474-14-22.
    Results Reference
    derived

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    WBV and Acute Lateral Ankle Sprain

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