Synergistic Benefits of MCE and BT in Sacroiliac Joint Dysfunction: A Randomized Controlled Trial

Sacroiliac Joint Dysfunction Clinical Trial

Official title:

Synergistic Benefits of Motor Control Exercises and Balance Training in Sacroiliac Joint Dysfunction: A Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06062459
• Other study ID #: IE/IIMS&R/2022/87
• Status: Completed
• Phase: N/A
• Start date: November 1, 2022
• Est. completion date: September 20, 2023

Study information

• Verified date: September 2023
• Source: Najran University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This research aimed to ascertain the combined and individual efficacies of MCE and BT in alleviating SIJD symptoms.

Description:

The study will be based on a four-arm parallel group randomized control design. one hundred and twenty participants with SIJD will be recruited from the Physiotherapy department, at Integral University, India. Study objectives and procedure will be properly explained and written informed consent will be obtained at the beginning of the study. All the participants will be randomly divided into four groups A, B, C, and D. Experimental group A will be receiving the hot pack, Stretching exercise, and MCE intervention, group B will receive the hot pack, Stretching exercise, and BT exercise and Group C will be receiving the hot pack, Stretching exercise, and MCE & BT intervention, control group D will receive the hot pack, Stretching exercise intervention.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 120
• Est. completion date: September 20, 2023
• Est. primary completion date: August 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years to 60 Years

Eligibility

Inclusion Criteria:

• Age-30-60 Years

• sacroiliac joint pain (>3 months)

• Presence of pain exacerbated as a result of bending laterally or backward

• Positive results on at least 2 of the pain-provocation tests [FABER, Posterior shear and Gaenslen pain provocation tests) and one of the motion palpation tests (ie, Gillet and forward flexion tests)

Exclusion Criteria:

• past or current history of surgery or major trauma to spine, pelvis, lower limb, chest or abdomen in the past 12 months

• lower extremity musculoskeletal disorders; known localized spinal pathology

• known congenital anomalies of hip, pelvis or spine that limits mobility

• known systematic arthropathy, neuropathy or metabolic disorder

• Presence of other causes of LBP such as lumbar discopathy and spinal stenosis discovered via clinical examination and MRI scanning

• pregnancy

Related Conditions & MeSH terms

• Joint Diseases
• Sacroiliac Joint Dysfunction

Intervention

Other:
• Motor Control Exercise
Motor control exercises focusing on the activation and control of deep spinal muscles
• Balance Training
Balance training exercises on to enhance proprioception and stability
• Control Group
Participants received hot pack and stretching exercise

Locations

Country	Name	City	State
India	Integral University Hospital	Lucknow	Uttar Pardesh
Saudi Arabia	Hashim Ahmed	Najran	Najran

Sponsors (1)

Lead Sponsor	Collaborator
Najran University

Countries where clinical trial is conducted

India,  Saudi Arabia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain Intensity	The pain intensity was assessed Using a numeric pain rating scale (NPRS), It's a 11 point scale, where zero indicates no pain and 10 indicates severe pain	6 Weeks
Primary	Functional disability	Functional limitation was assessed by using Oswestry disability Index questionnaire Each section is scored on a 0-5 scale, 5 representing the greatest disability.	6 Weeks
Primary	self-reported measure of health	It comprises 36 questions that cover eight domains of health	6 Weeks