Other Clinical Trial - Exercise & Two Different Kinesiotape Applications

Status Recruiting

Clinical Trial Summary

This study is a randomized controlled study. 75 patients between the ages of 20-50 who were diagnosed with sacroiliac joint dysfunction will be included in the study. 25 patients will be given a home exercise program that strengthens the waist and hip girdle (to be shown once in the hospital by a physiotherapist and the form of the exercises will be given), 25 patients will be given kinesiology taping with inhibition technique with the exercise program, and 25 patients will be given kinesiology taping with fascia correction technique with the exercise program. Patients will do the exercises once a day for 1 month. In kinesiology taping with the inhibition method, an I-shaped tape of 15-20 cm in length will be applied on the sacroiliac joint on both sides without stretching the ends with 50% stretching in the middle. In addition, a 25-30 cm long I band will be applied over the right spina iliaca posterior superior, towards the left spina iliaca posterior superior. In the facia correction technique, 2 bands with no cut ends, a 10-15 cm web-shaped band divided into 4 or 5 parts with a width of 1-15 cm will be applied cross over the sacroiliac joint, without stretching the ends with 50% stretching in the middle. Gillet test (evaluation of sacroiliac joint movement with single hip flexion), Gaenslen test (pain provocation with passive hip flexion), Patrick test (provocation of pain with hip flexion, abduction and external rotation), standing flexion test (evaluation of sacroiliac joint movement with forward flexion), sacroiliac compression and distraction test (provocation of pain with anterior pelvic compression or distraction), long sitting test (pain in the sacroiliac joint after sitting for more than 30 minutes), posterior shear test (provocation of pain with hip flexion and adduction) will be applied to the patients. The patients' resting and moving pain levels will be measured using the Visuel Analog Scale (VAS). Pain duration in the last week will be questioned and noted. Global Assessment of the Patient's Self within the last 1 week will be made over VAS. Oswestry Disability Index (ODI) will be applied to determine the level of disability. Evaluations will be made before, 15 days after and 1 month after treatment.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Joint Diseases
Sacroiliac Joint Somatic Dysfunction

Clinical Trial Details

NCT number	NCT04829513
Study type	Observational
Source	Ufuk University
Contact	saime ay
Phone	05325138760
Email	saimeay@yahoo.com
Status	Recruiting
Phase
Start date	December 1, 2016
Completion date	December 1, 2022

View Details

See also
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Active, not recruiting	`NCT03507049` - Sacroiliac Joint Fusion Versus Sham Operation for Treatment of Sacroiliac Joint Pain	N/A
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Withdrawn	`NCT04534829` - Fluoroscopic vs Ultrasound Guided Sacroiliac (SI) Joint Radiofrequency Ablation	Phase 3
Completed	`NCT04519840` - Diastasis Recti Abdominis Association With Sacroiliac Joint and Pelvic Floor Dysfunction in Postpartum C-section Women
Completed	`NCT04717401` - Comparison Between Strain-counterstrain and Muscle Energy Technique in Sacroiliac Joint Dysfunction	N/A
Terminated	`NCT04218838` - Comparison of CornerLoc SI Joint Stabilization and Steroid Injections for Sacroiliac Joint Dysfunction	N/A
Completed	`NCT05347537` - Effects of Mulligan's Mobilization With and Without Clamshell Exercises in Sacroiliac Joint Dysfunction	N/A
Recruiting	`NCT04381208` - Medical Record, Physical and Neurological Data That Orient to the Diagnosis of Sacroiliac Joint Dysfunction
Recruiting	`NCT05944861` - Combination of Fluoroscopy and Ultrasonography Guidance in Sacroiliac Joint Injections	N/A

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Exercise and Two Different Kinesiotape Applications in Patients With Sacroiliac Joint Dysfunction

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms