Reliability and Validation of 3-D Electromagnetic Tracking During Pelvic Floor Muscle (PFM) Activation - a Pilot Study
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Purpose
Now a days the ultrasound is seen as a valid and reliable measurement tool to test the Pelvic Floor Muscle (PFM) movement (Sherburn, Murphy, Carroll, Allen, & Galea, 2005). The hypothesis is that the electromagnetic tracking system, TrakSTARTM, can measure the PFM movement in an equal or even more precise way. The TrakSTARTM will have the advantage to be used in measuring functional movements. In this Master thesis the hypothesis is to show a good reliability by trampoline jumping (physical activity).
| Condition |
|---|
|
Pelvic Floor Dyssynergia |
| Study Type: | Observational |
| Official Title: | Reliability and Validation of 3-D Electromagnetic Tracking During Pelvic Floor Muscle (PFM) Activation - a Pilot Study |
- the way in x-y coordinates for the pelvic floor mouvement measured by the ultrasonography and TrakSTAR [ Time Frame: one year ] [ Designated as safety issue: No ]the mouvement of the pelvic floor is measured similtanous by the ultrasound and the TrakSTAR
- EMG [ Time Frame: one year ] [ Designated as safety issue: No ]EMG will measure the contraction of the plevic floor
| Estimated Enrollment: | 20 |
| Study Start Date: | August 2012 |
| Estimated Study Completion Date: | May 2013 |
| Estimated Primary Completion Date: | February 2013 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
| 20 healthy women |
Detailed Description:
There will be two measurements. One measurement of MVIC and quick flicks will be done in a standing and supine position with 3 repetitions. The TrakSTARTM, Ultrasound, surface EMG and Accelerometer will measure the PFM movements and activation simultaneously. The Ultrasound is measured from one tester (to guaranty a high intratester reliability) (Sherburn et al., 2005).
TrakSTARTM, surface EMG and Accelerometer will measure 3 Trampoline jumps. The measurements will be done once during one hour. The women will insert the vaginal probe by themselves and stay dressed during the measurement procedure. The measurements will be done in a standardized way. All the arrangements are made to ensure the hygiene requirements.
Eligibility| Ages Eligible for Study: | 18 Years to 35 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
healthy women, students of the University of Applied Sciences Health
Inclusion Criteria:
- women
- aged between 18 and 35 years
- anamnestically healthy
- nulliparous and
- a BMI between 18 and 30
Exclusion Criteria:
- latex and nickel allergy
- anamnestically current pregnancy
- menstruation
- urogenital operations
- anal operations
- vaginal infections
Contacts and Locations| Contact: Helene Moser, Msc in study | 0041787752118 | helmos69@gmail.com |
| Switzerland | |
| Inselspital | Not yet recruiting |
| Bern, Switzerland, 3010 | |
| Contact: Helene Moser, MSc in study 0041787752118 helmos69@gmail.com | |
| Study Chair: | Lorenz Radlinger, PhD | Berner Fachhochschule Gesundheit, Bern, Switzerland |
More Information
Publications:
| Responsible Party: | Helene Moser, Physiotherapist, Moser, Helene |
| ClinicalTrials.gov Identifier: | NCT01590927 History of Changes |
| Other Study ID Numbers: | MScPTHM |
| Study First Received: | April 27, 2012 |
| Last Updated: | May 2, 2012 |
| Health Authority: | Switzerland: Ethikkommission |
Keywords provided by Moser, Helene:
|
pelvic floor ultrasonography |
Additional relevant MeSH terms:
|
Ataxia Dyskinesias Neurologic Manifestations Nervous System Diseases Signs and Symptoms |
ClinicalTrials.gov processed this record on May 21, 2013