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
About this trial
This is an interventional treatment trial for Postural Control
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
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
NCT ID
NCT01702597
First Posted
October 3, 2012
Last Updated
October 4, 2012
Sponsor
Ludwig-Maximilians - University of Munich
Collaborators
Medical University Innsbruck
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
Learn more about this trial
WBV and Acute Lateral Ankle Sprain
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