Clinical Trials Logo

Sacroiliac Joint Dysfunction clinical trials

View clinical trials related to Sacroiliac Joint Dysfunction.

Filter by:

NCT ID: NCT05863390 Recruiting - Clinical trials for Sacroiliac Joint Dysfunction

Effectiveness of McKenzie and Trochanteric Belt With CT Therapy to Reduce Pain and Dysfunction of SI Joint

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

To determine the effectiveness of McKenzie exercises and trochanteric belt with conventional physical therapy to reduce pain and dysfunction of Sacroiliac joint (SIJ) in pregnant women

NCT ID: NCT05855304 Completed - Clinical trials for Sacroiliac Joint Dysfunction

Comparison Of The Sacroiliac Manipulation And Kinesiological Tape In Basketball Players

Start date: May 1, 2023
Phase: N/A
Study type: Interventional

In the USA, basketball is the most popular team sport for boys and girls enrolled in the 2003-2004 school year. Many countries offer opportunities for young people to learn the game in a variety of settings, from physical education classes, school competitions, public and private sports organizations to community entertainment programmes. While the USA has long been seen as the dominant power in basketball, recent results in competitions such as the 1988 and 2004 Men's Olympic Games and 2002 World Championships show the rest of the world is closing the gap. Basketball continues to spread around the world, thanks to ongoing development programs for children and youth .

NCT ID: NCT05809206 Not yet recruiting - Clinical trials for Sacroiliac Joint Dysfunction

Gluteus Maximus Versus Gluteus Medius Strength On Back Muscles Performance In Patients With Sacroiliac Dysfunction

Start date: April 10, 2023
Phase: N/A
Study type: Interventional

This study will be conducted to compare between the effect of glutes maximus and glutes medius muscles strength on back muscle performance in patients with Sacroiliac joint dysfunction.

NCT ID: NCT05786118 Completed - Clinical trials for Chronic Low-back Pain

The Effects of Sacroiliac Joint Dysfunction on Gait and Disability

Start date: March 21, 2023
Phase:
Study type: Observational [Patient Registry]

It has been reported that gait coordination changes in patients with chronic low back pain, walking slower, taking shorter steps and having asymmetrical stride lengths compared to their healthy peers. In addition to many factor cause gait dysfunction, sacroiliac joint dysfunction might be one of reason of these problems. A study examining the effects of sacroiliac joint dysfunction on gait and disability in individuals with chronic low back pain has not been found in the literature. Therefore, the aim of this study is to evaluate the gait parameters and disability of individuals with chronic low back pain and to reveal their relationship with sacroiliac joint dysfunction.

NCT ID: NCT05712850 Enrolling by invitation - Clinical trials for Sacroiliac Joint Dysfunction

Clinical Outcome and Fusion Results Using the SiJoin® Transfixing Sacroiliac Fusion Device

Start date: January 19, 2023
Phase:
Study type: Observational

The purpose of this clinical study is to evaluate fusion of the SI joint(s) and any reduction in VAS pain scores in a prospective cohort of patients utilizing the SiJoin® Transfixing Sacroiliac Fusion Device in patients that received sacroiliac fusion, without ancillary stabilization devices.

NCT ID: NCT05479266 Completed - Low Back Pain Clinical Trials

Comparison of Muscle Energy Techniques and Myofascial Release on Low Back Pain Due to Sacroiliac Joint Dysfunction

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

The aim of this research is to compare the effects of Muscle Energy Techniques and Myofascial Release on Lumbar Range of motion, pain and disability in patients of low back pain due to Sacroiliac Joint Dysfunction, Randomized controlled trials were done at a private clinic, The Health Professionals Bahria Town Phase 6, Islamabad. The Sample Size was 30. The subjects were divided into two groups, 15 subjects in Interventional group A receiving conventional physical therapy treatment alongside METs for hamstrings, iliopsoas and piriformis muscle while the other 15 subjects in Interventional group B receiving conventional physical therapy treatment with direct myofascial release of hamstrings, iliopsoas and piriformis muscle. study duration was of 6 months. Samling technique applied was non.probability sampling. Only females of age group 40-55 yrs having sacroiliac joint pain with limited lumbar range of motion were reduced. Tools used in the study were Numeric Pain Rating Scale(NPRS), Modified Oswestry Disability Index(MODI), Pelvic and bubble Inclinometer. Data was analyzed through SPSS 21.

NCT ID: NCT05404984 Not yet recruiting - Clinical trials for Sacroiliac Joint Dysfunction

Effects of Core Stabilization Exercises With and Without Dry Cupping in Patients With Sacroiliac Joint Dysfunction

Start date: June 2022
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effects of core stabilization exercises with and without dry cupping on pain and disability in patients with sacroiliac joint dysfunction.

NCT ID: NCT05356650 Recruiting - Clinical trials for SACROILIAC JOINT DYSFUNCTION

Mulligan's Mobilization and Proprioceptive Neuromuscular Facilitation Technique in Sacroiliac Joint Dysfunction

Start date: April 15, 2022
Phase: N/A
Study type: Interventional

This study will aim to compare the effects of mulligan mobilization and PNF on pain and disability with patients of SIJ dysfunction and will be helpful for clinical physiotherapist to choose more effective treatment protocol for patients as there are fewer researches on comparison of these techniques.

NCT ID: NCT05018780 Completed - Clinical trials for Sacroiliac Joint Dysfunction

Muscle Energy Techniques and Sacral Manipulation on Pain, Functional Disability and Quality of Life

Start date: July 1, 2021
Phase: N/A
Study type: Interventional

- The study will be randomized clinical trial. This study will be conducted in University of Lahore Teaching Hospital, Lahore, Pakistan. A sample size of 84 will be randomly allocated into two experimental groups, (42 participants in each group), by lottery method. The participants, randomly allocated to the experimental group A, will receive Muscle Energy Technique (METs), Post isometric relaxation technique specifically, in addition with routine physical therapy as TENS, Hot pack, and strengthening exercises. METs will be performed on piriformis, iliopsoas, erector spine muscles, 1 set of 5 repetitions and 10 seconds hold. - Participants in experimental group B, will get Sacroiliac joint manipulations with routine physical therapy by principal investigator. - Both experimental groups will receive twelve treatment sessions and those will be given over a period of six weeks (2 sessions per week, each session of 30-40 minutes). - Assessor will take outcome measures at baseline and at the end of 6th treatment week through Short Form McGill Pain Questionnaire, Roland-Morris Low Back Pain & Disability Questionnaire and Short Form Survey; SF-20.

NCT ID: NCT04824534 Completed - Clinical trials for Sacroiliac Joint Dysfunction

Motion Analysis in Sacroiliac Joint Dysfunction

MASSIF
Start date: March 1, 2021
Phase:
Study type: Observational [Patient Registry]

Rationale: The sacroiliac joint (SIJ) is increasingly being recognized as a potential cause of chronic low back and buttock pain. The SIJ is affected in 14-22% in patients presenting with this pain. Conservative treatment options include oral analgesic use, physical therapy, radiofrequency denervation and intraarticular steroid injections. When non-surgical treatment remains ineffective, surgical intervention is a reasonable option in the form of minimally invasive sacroiliac joint fusion (MISJF). Recent literature suggests that imbalance and sagittal sacropelvic morphology can occur in patients with SIJ dysfunction. Using motion analyses, the investigators want to evaluate full movement patterns in SIJ patients. Potentially, changes in these parameters can be observed before and after MISJF surgery. Objective: To determine spatiotemporal parameters, pelvic obliquity, center of gravity and load capacity in patients suffering from SIJ dysfunction before and after MISJF surgery. Movement parameters will also be determined in healthy individuals to compare with patients suffering from SIJ dysfunction. Methods: This prospective cohort study will include patients enlisted for MISJF surgery because of SIJ dysfunction. Spatiotemporal parameters, pelvic obliquity, center of gravity and load capacity will be examined before and 3 months after surgery in a professional Motion Lab. Movement parameter of healthy individuals will also be evaluated at the Motion Lab. All data will be analyzed using MATLAB software.