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

Sacroiliac Joint Somatic Dysfunction Clinical Trial

Official title:

Exercise and Two Different Kinesiotape Applications in Addition to Exercise in Patients With Sacroiliac Joint Dysfunction: A Randomized Controlled Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04829513
• Other study ID #: 15112016-5
• Status: Recruiting
• Start date: December 1, 2016
• Est. completion date: December 1, 2022

Study information

• Verified date: April 2021
• Source: Ufuk University
• Contact: saime ay
• Phone: 05325138760
• Email: saimeay[@]yahoo.com
• Is FDA regulated: No
• Study type: Observational

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 75
• Est. completion date: December 1, 2022
• Est. primary completion date: December 1, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 50 Years

Eligibility

Inclusion Criteria:

• Patients with sacroiliac joint dysfunction between the ages of 20-50
• Hip and low back pain that does not exceed the 5th lumbar vertebra for at least 3 months
• Patients with pain radiating 3 cm above and 10 cm below the spina iliaca posterior superior
• Patients who have not received medical treatment in the last 6 months

Exclusion Criteria:

• Patients with sacroiliac and inflammatory disease
• Patients with polyarthrosis, herniated disc, severe symptomatic disc degeneration, spinal stenosis and spondyloarthrosis.
• Patients with a history of pelvic trauma
• Patients with metabolic bone disease, infection, malignancy, pregnancy
• Patients with open wounds in the lumbar and sacral area

Related Conditions & MeSH terms

• Joint Diseases
• Sacroiliac Joint Somatic Dysfunction

Intervention

Other:
• kinesio taping
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.

Locations

Country	Name	City	State
Turkey	Ufuk University	Ankara

Sponsors (1)

Lead Sponsor	Collaborator
Ufuk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain levels at Visuel Analog Scale	The patients' resting and moving pain levels will be measured using the Visuel Analog Scale. Patients will be asked to mark their pain levels on a visual analog scale of 0-10 cm. Higher values indicate more pain.	1 month
Primary	Pain duration in the last week	Pain duration in the last week	1 week
Primary	Global Assessment of the Patient's self at Visuel Analog Scale	Global Assessment of the Patient's Self within the last 1 week will be made over Visuel Analog Scale. Patients will be asked to mark their global assessment on a 0-10 cm visual analog scale. Higher values indicate better result.	1 week
Primary	Oswestry Disability Index	Oswestry Disability Index (ODI) will be applied to determine the level of disability. It is a scale consisting of 10 questions, each scored between 0 and 5 points. The minimum score is 0 and the maximum score is 50. Higher results indicate worse functional status.	1 month