Aveiro University
Aveiro, 3810-193, Portugal
NCT Number: NCT06710535
Sacroiliac joint dysfunction (ASI) is an alteration in the normal biomechanics of the joint, which leads to hypomobility or hypermobility of that joint. It is one of the most common causes of misdiagnosis in low back pain and when not treated correctly, it often evolves into chronic pain (30% to 42%) and disability. Manipulating the dysfunctional ASI appears to result in benefits and significantly positive changes at various levels, in all segments of the human body. With this investigation, the investigators intend to clarify and deepen the possible correlation between the changes that normally accompany this dysfunction, as well as its possible reversibility with its normalization.- Objectives
* The investigators will essentially have two main objectives:
1. Mapping of the most evident symptomatic changes, when sacroiliac joint dysfunction is present, in terms of pain, balance and gait ; 2. To try to understand the immediate, global and short-term effect of ASI manipulation, studying the cumulative effect of six sessions and the possible interrelationship between the changes recorded.
- Study design Quantitative, with experimental study design, RCT, with the sample comprising individuals with SIJ dysfunction, where all participants in study 2 will be randomly allocated to the experimental, control and placebo groups. It will be carried out at the University of Aveiro facilities.
Initially, the investigators will map the changes present at a physical level, followed by manipulation, evaluating the immediate effect, measuring the degree of pain, unipodal balance and satisfaction with the treatment.
The investigators will then evaluate the effect of 3 sessions, on a weekly basis, for 3 weeks.
- Material and methods
The investigators will make use of: * Standing flexion test, to define the laterality of the dysfunction; * VAS , to subjectively assess pain; * Pressure algometer, to objectively assess pain ; * Force Platform, to assess balance; * G-Walk, for gait assessment; * PGIC, to assess satisfaction with treatment ;
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Notify Me18 year–30 year
All sexes
Interventional
Not applicable
Aveiro, 3810-193, Portugal
Procedures to be used in the Experimental Study Material and methods
Reception of participants, with a clear explanation of the objectives and procedures to be used in the pilot study, asking them to fill out:
Participants who test positive in at least 4 of the 5 tests mentioned above will be selected to participate in the following studies:
Variables :
Instruments : -
Clinical trial (RCT), in which participants will be randomly divided into 3 groups:
Variables :
Instruments:
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The participants will receive one session of manipulation if in the experimental group. It should be mentioned that the technique will be carried out by a physiotherapist with a history of more than 10 years of manual therapy. For instance, to correct right anterior innominate rotation, the participant will be made to lie on the side so that the affected side is upward. The physiotherapist will stand in front of the participant; first we will put their shoulders, pelvis and lower limbs in neutral position and place the right hand on the anterior superior iliac spine (ASIS) and the left hand on the ischium tuberosity and with a rotational movement of the hands, the physiotherapist will rotate the ilium posteriorly. At the end of the range, we will replace the position of hands and place the left forearm on the ischium tuberosity and place the right hand on the upper participant's shoulder and will move it toward the bed at the end of the range in exhalation a thrust will be executed.
The participants will receive one session of sham manipulation if in the sham group. For instance, to correct right anterior innominate rotation, the participant will be made to lie on the side so that the affected side is upward. The physiotherapist will stand in front of the participant; first we will put their shoulders, pelvis and lower limbs in neutral position and place the right hand on the anterior superior iliac spine (ASIS) and the left hand on the ischium tuberosity and with a rotational movement of the hands, the physiotherapist will rotate the ilium posteriorly. At the end of the range, we will replace the position of hands and place the left forearm on the ischium tuberosity and place the right hand on the upper participant's shoulder and will move it toward the bed at the end of the range in exhalation, the physiotherapist will pretend to execute a thrust.
Time frame: From enrollment the assessment will be executed, before and immediately after the intervention taking approximately one week]
Pain will be assessed with the Visual Analogue Scale (VAS), a horizontal line graded 0 (better outcome) to 10 (worse outcome).
Time frame: From enrollment the assessment will be executed, before and immediately after the intervention taking approximately one week
Pressure algometer
Time frame: From enrollment the assessment will be executed, before and immediately after the intervention taking approximately one week]
Assess single-leg balance with a force platform
Time frame: From enrollment the assessment will be executed, before and immediately after the intervention taking approximately one week
Assess gait parameters with G-Walk, a wearable inertial sensor for motion analysis
Time frame: Immediately after the last treatment
PGIC ( Patient Global Improvement Change Scale ) - is an instrument for measuring and evaluating the global perception of change and satisfaction with treatment, used in any health condition, unidimensional, with a scoring system on a positive orientation scale from 1 to 7, with a completion time of 1 minute*.
Aveiro University
Other
Global Changes Associated With Sacroiliac Joint Dysfunction and Its Reversal by Manipulation - A Randomized Controlled Trial
Acronym: LOUIS
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