Clinical Trials Logo

Clinical Trial Summary

First, this study aims to use the straight leg raising test (SLR) and the knee angle extension test (KEA) test associated to a structural differentiation to determine the limitation of the lower limb (muscular or nervous) in asymptomatic subjects. Second, this study will try to determine the most efficient exercice to increase range of motion of the lower limb in function of subjects limitation type (muscular, nervous,) using neural mobilization (sliders or tensioners) and muscle stretching. Two groups will be constituted for each test (SLR and KEA) based on the limitation defined during the test: Group 1: Muscle limitation Group 2: Neural limitation Each group will be subdivided in four subgroups depending on the intervention participants will receive: - subgroup 1: Muscle stretching group - subgroup 2: Neural tensioner group - subgroup 3: Neural slider group - subgroup 4: Control group Participants from groups 1,2 and 3 will be asked to do an exercice every day during 31 days, independently of their subgroup allocation. Participants from group 1 will perform a muscle stretching technique during 20 second twice a day. Participants from group 2 will do 10 repetitions of tensioner twice a day. Participants from group 3 will do 10 repetitions of a slider twice a day. Subgroup comparisons of the evolution of the range of motion during SLR and KEA before and after the month of exercice will determine which technique is the most efficient for a specific type of limitation.


Clinical Trial Description

Objectives: First, this study aims to use the straight leg raising test (SLR) and the knee angle extension test (KEA) test associated to a structural differentiation to determine the limitation of the lower limb (muscular or nervous) in asymptomatic subjects. Second, this study will try to determine the most efficient exercice to increase range of motion of the lower limb in function of subjects limitation type (muscular, nervous,) using neural mobilization (sliders or tensioners) and muscle stretching. Procedures: All the participants will attend two assessment sessions i.e., at baseline and after 31 days, expect for participants allocate in the control group, who will be also tested 48 to 72 hours after the first evaluation in order to determine the test/retest reliability of the structural differentiation. Baseline session: During the baseline session, demographics data will be collected (age, gender, height and weight) and a check for exclusions criteria will be conducted. The identification of the dominant lower limb will then be performed by asking participants to shoot on a ball The Identification of the limitation The leg to be tested will be the dominant one in half of the population while the other half will have the non-dominant leg tested. In order to standardize the assessments, participants will be placed supine with the cervical spine in neutral position and with the upper part of head at the edge of the examination table (Table with a moveable head set) with both hands placed under the lumbar spine. Furthermore, a belt will be place to fix the pelvis to the examination table at the level of the anterior superior iliac spine. The SLR and the KEA tests will then be performed. For standardization purposes, the same sequence of testing will be used at each session for the same participant (first SLR and second KEA or conversely), but sequences of tests will be used alternatively between participants to avoid methodological bias. Participants will be asked to say "stop" when a discomfort appears at the posterior part of the tight, the calf, the knee, the buttock or in the foot. For the SLR, the investigator will induce a hip flexion movement, while maintaining the knee in extension, with one hand placed on the distal anterior part of the tight and with the other hand located on the posterior distal part of the leg (9). For the KEA a labrique inclinometer will be placed on the anterior part of the tight allowing the investigator to control that a 90° of hip flexion is maintained, while he will passively induce a knee extension. A second investigator will evaluate the hip and knee range of motion during the SLR and KEA respectively, with an electronical inclinometer using the more proximal part of the tibial tuberosity as a marker for the device placement. While maintaining the ipsilateral SLR or KEA, a structural differentiation (SD) will be used to identify the structure related to patient discomfort. In order to do the SD, 2 stages will be conducted: first a third investigator will passively induce a flexion of the thoracic spine using the movable cranial part of the table and will manually move the cervical spine in flexion. The participant will then be invited to define if the discomfort in the limb tested is modified using the following predefined descriptors: increase, decrease, not changed, different location of the symptoms or a combination of these. In the second stage, the third investigator will induce a passive extension of the thoracic and cervical spine and participants will be asked to report any potential changes of the lower limbs discomfort using the same descriptors as mentioned previously. Interpretation of the tests and group allocation: If both stages of the SD did not change the lower limb discomfort, a "muscle limitation" will be suspected. Nervous structures will be suspected to be the limiting factor, if the discomfort was increased during the flexion part of the SD and decreased during the extension part. Thereby, participants will be divided in two groups: the "Nerve group"will included the participants in whom nervous structures were suspected to be the limiting factor after SD ; the "Muscle group" will include participant for whom a "muscle limitation" was suspected. Exercise allocation will be done by another investigator in a separate room. In each groups ("Nerve" or "Muscle"), participants will be randomized in one of the four following subrgroups: - subgroup 1: Muscle stretching group - subgroup 2: Neural tensioner group - subgroup 3: Neural slider group - subgroup 4: Control group Participants from groups 1,2 and 3 will be asked to do an exercice every day during 31 days, independently of their subgroup allocation. Participants from group 1 will perform a muscle stretching technique during 20 second twice a day. Participants from group 2 will do 10 repetitions of tensioner twice a day. Participants from group 3 will do 10 repetitions of a slider twice a day. Subgroup comparisons of the evolution of the range of motion during SLR and KEA before and after the month of exercice will determine which technique is the most efficient for a specific type of limitation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05899244
Study type Interventional
Source University of Liege
Contact
Status Completed
Phase N/A
Start date June 15, 2023
Completion date October 4, 2023

See also
  Status Clinical Trial Phase
Completed NCT03361592 - The Immediate Effects of Spinal Manipulative Therapy on Kinetic and Kinematic Symmetry. N/A
Completed NCT04665193 - An Approach to Screening for COVID-19 at Vancouver Airport N/A
Not yet recruiting NCT02238028 - Intervention Study on the Health Effects of Wearing Particulate Filtering Respirators N/A
Completed NCT03455933 - Action Mechanisms of Shock Waves on Pain N/A
Completed NCT05377164 - Long Term Effects of Different Dietary Protocols on Determinants of Health in Patients' Lymphocytes
Completed NCT04480398 - Efficacy and Safety of Guduchi Ghan Vati for Covid-19 Asymptomatic Patients
Completed NCT05210231 - Effects of Transcranial Direct Current Stimulation (tDCS) on Rotator Cuff Fatigue. N/A
Completed NCT04387032 - Impact of Manipulation of Sacroiliac Joints on the Static Balance of the Body N/A
Recruiting NCT03237039 - Classification of the Sagittal Profile of the Spine in Asymptomatic Elderly Subjects N/A
Completed NCT06048237 - Investigating Diaphragm Thickness and Mobility in Healthy Parous and Nulliparous Volunteers Using RUSI
Completed NCT04775628 - Forces and Translation Distance During an Inferior Glide of the Shoulder N/A
Not yet recruiting NCT06395675 - Clinical Evaluation of the ID NOW™ CT/NG Test N/A
Recruiting NCT06215040 - The Treatment Effect for Asymptomatic Common Bile Duct Stone
Recruiting NCT06197945 - Effects of Mulligan Bent Leg Raise With and Without Bowen Therapy on Hamstring Tightness in Asymptomatic Adults N/A
Completed NCT04741893 - Anal Canal Functional Assessment Using EndoFLIP N/A
Not yet recruiting NCT05911828 - A Study to Determine Safety, Tolerability, and Pharmacokinetics of Different Orally Administered Regimens of the Combination ZY19489-Ferroquine in Adult Asymptomatic Plasmodium Falciparum Carriers Phase 1
Completed NCT04785079 - Instrument Assisted Soft Tissue Mobilization Effect on Blood Flow N/A
Completed NCT04360668 - Muscle Energy Techniques and Trigger Point Therapy in Asymptomatic Persons With Latent Trigger Point N/A
Completed NCT04367740 - ScreenNC, a Study to Determine the Number of Asymptomatic Individuals Who Have Antibodies to the Virus That Causes COVID-19
Terminated NCT04346667 - Post-Exposure Prophylaxis for Asymptomatic SARS-CoV-2 COVID-19 Patients With choloroquinE Compounds Phase 4