]>
IRCT20251017067658N1 IRCT 2026-01-07 Vice President for Research, Bu-Ali Sina University, Hamadan The effect of comprehensive core stability and lumbopelvic stabilization exercises on Plantar pressure variables, pain, and quality of life patients with chronic non-specific low back pain The effect of comprehensive core stability and lumbopelvic stabilization exercises on Plantar pressure variables, pain, and quality of life patients with chronic non-specific low back pain 2026-01-10 anticipated 40 Complete https://irct.ir/trial/88481 interventional Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: Randomization was done by drawing lots. We wrote the titles of control and experimental on pieces of paper and asked the subjects to each pick one of them, Blinding description: The data analyst will not be aware of the group division (group information will be provided to the data analyst in the form of groups 1 and 2 for each participant with a code). N/A Chronic non-specific low back pain. Intervention 1: Intervention group: Intervention group: Comprehensive core stability exercise protocol with lumbopelvic stabilization in the present study was performed for eight weeks, three sessions per week, and each session lasted 60 minutes. These exercises included abdominal pull-in maneuver, leg bent-over abdominal, reverse crunch, clamshell, bridge, single-leg bridge, side bridge, modified sit-up, bird dog, leg extension, kick bag, and hip abduction to the side. Intervention 2: Control Group: Control Group: Initially, all tests were taken from them and the people in this group did not participate in any rehabilitation intervention and simply lived their normal lives with daily activities during these 8 weeks, and then after 8 weeks, the post-test was taken from them. Yes - There is a plan to make this available What will be shared: The measured data files will be shared by the testers after the study is completed, if needed. When: The period begins one year after the publication of results and articles. To whom: Researchers and researchers whose field of work is similar to the present research and who are employed in universities. Conditions: The data from this study will only be made available to other researchers for comparison with future studies, and the use and analysis of the data is prohibited. Where to obtain: Email address m.azizpour@phe.basu.ac.ir How to obtain: A complete explanation of the research should be provided and the details of the use of the data should also be fully explained. Comments:
public Ali Yalfani
Shahid Mustafa Ahmadi Roshan Street, Bu Ali Sina University
Hamedan Iran (Islamic Republic of) ۳۸۶۹۵-۶۵۱۷۸ +98 81 3140 2863 yalfani@basu.ac.ir Bu Ali Sina University scientific Ali Yalfani
Shahid Mustafa Ahmadi Roshan Street, Bu Ali Sina University
Hamedan Iran (Islamic Republic of) ۳۸۶۹۵-۶۵۱۷۸ +98 81 3140 2863 yalfani@basu.ac.ir Bu Ali Sina University Iran (Islamic Republic of) A history of more than three months of back pain, physician confirmation of chronic non-specific back pain spinal deformities no acute deformities in the lower extremities or soles of the feet People with chronic back pain in the age range between 30 and 50 years 30 years 50 years Female Having scoliosis advanced osteoporosis advanced cardiovascular disease uncontrolled blood pressure severe deformity in the lower limbs and soles of the feet, fractures in the spine unwillingness to participate in exercises M54.5 Low back pain Treatment - Other Treatment - Other Intervention group: Intervention group: Comprehensive core stability exercise protocol with lumbopelvic stabilization in the present study was performed for eight weeks, three sessions per week, and each session lasted 60 minutes. These exercises included abdominal pull-in maneuver, leg bent-over abdominal, reverse crunch, clamshell, bridge, single-leg bridge, side bridge, modified sit-up, bird dog, leg extension, kick bag, and hip abduction to the side. Control Group: Control Group: Initially, all tests were taken from them and the people in this group did not participate in any rehabilitation intervention and simply lived their normal lives with daily activities during these 8 weeks, and then after 8 weeks, the post-test was taken from them. Pain. Timepoint: Pre-test and post-test, meaning before the start of the first practice session and one day after the end of the last practice session. Method of measurement: VAS questionnaire. Quality of life. Timepoint: pre test & post test. Method of measurement: The Short Form Health Survey (SF-36) questionnaire. Vice President for Research, Bu-Ali Sina University, Hamadan Approved 2025-10-05 Research Ethics Committees of Bu Ali Sina University-Hamedan Hamedan, Shahid Mustafa Ahmadi Roshan Street Hamrdan Hamadan Iran (Islamic Republic of)