- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04685863
Slump Physiotherapy : Effect on the physiologicAl Knee Extension Range-of-motion (SPEAKER)
Effect of Neurodynamic Mobilization Techniques on Knee Extension Range of Motion of Asymptomatic Young Students: a Prospective, Comparative Study.
Background: The neurodynamics technique seems interesting for increased lower limb flexibility of the lower limbs in healthy subjects. The objective of this study is to assess the physiological effects of the SLUMP sliding technique on the range of knee extension during the SLUMP test.
Methods: 60 physiotherapy students perform measurements during three tutorials. The first involves training in evaluation techniques. The second involves mobilizing the knee, out of the SLUMP position. The third tutorial includes neuronal mobilization in SLUMP.
Knee extension in SLUMP position is measured immediately after completing techniques. The mobilization amplitudes (degrees) will be compared between the techniques by a Student test on paired series, each subject being his own control.
Discussion: The results of this study will provide evidence for the physiological effect of SLUMP sliding techniques performed by physiotherapy students on the range of knee extension during the SLUMP test in asymptomatic subjects.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Timothée Gillot, PhD
- Phone Number: 02 32 88 06 71
- Email: Timothee.Gillot@chu-rouen.fr
Study Contact Backup
- Name: valérie de La Moussaye
- Email: valerie.De-La-Moussaye@chu-rouen.fr
Study Locations
-
-
-
Rouen, France, 76000
- Recruiting
- ROUEN university hospital
-
Contact:
- Valérie de La Moussaye
- Phone Number: 0232888265
- Email: valerie.De-La-Moussaye@chu-rouen.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Students enrolled in second year of physiotherapy training in Rouen's physiotherapy Institute, taking part to neurodynamic technique course unit (CU 7)
- Ability to perform daily physiotherapy techniques, assessed by an accredited doctor from regional health agency and a medical examination during the first year of scholarship (occupational medicine service of Rouen's University hospital)
- French commonly spoken and red
- Aged 18 or older
- Registered to the national care & health system (Social security number)
- Willingness to take part to the study
Exclusion Criteria:
- Person denied of freedom by judicial or administrative decision
- Person requiring a guardian, guardianship or curators
- History of psychological disease/illness or sensorial disease preventing from understanding the recruitment conditions
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Knee extension angle achieved in SLUMP test position: - after a control technique during the second practical work (TD2)
Time Frame: day 14 from inclusion
|
degree
|
day 14 from inclusion
|
Knee extension angle achieved in SLUMP test position : - after neurodynamic sliding techniques in SLUMP during the third practical work (TD3)
Time Frame: day 21 from inclusion
|
degree
|
day 21 from inclusion
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Finger-to-floor distance
Time Frame: days 14 and 21 from inclusion
|
centimeter
|
days 14 and 21 from inclusion
|
Hamstring flexibility (passive knee extension test)
Time Frame: days 14 and 21 from inclusion
|
degree
|
days 14 and 21 from inclusion
|
Angle of knee extension achieved in SLUMP test between "active neurodynamic technique" group and "passive neurodynamic technique" group
Time Frame: days 14 and 21 from inclusion
|
degree
|
days 14 and 21 from inclusion
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Timothée Gillot, ROUEN university hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2020/0251/OB
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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