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IRCT2016070528809N1 IRCT 2016-12-30 Vice Chancellor for Research of Shiraz University of Medical Sciences The Effect of Tele-Rehabilitation Technology on chronic non specific low back pain - Randomised Clinical Trial of The Effect of Tele-Rehabilitation Technology on Pain, Functional Disability, Clinical Index of Balance and Quality of Life in Patients with Chronic Non-Specific Low Back Pain 2016-12-21 anticipated 20 Complete https://irct.ir/trial/23278 interventional Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Other design features: Randomly allocated using block randomization method. N/A chronic low back pain. Intervention 1: Intervention group: 5 educational videos will be produced including the stages of exercise and the exercise program will be sent to the intervention group through 12 sessions during 4 weeks (3 sessions per week) based on the treatment protocol. Each session takes 30 to 45 minutes. Each session has been designed in four parts: warm-up, preform exercise programs, cooling, questions and answers. Intervention 2: Control group: the control group will not participate in any specific treatment plan and receive only their usual care.
public Fatemeh Niknam
School of Management and Medical Informatics, Almas Building, No 29 Allay, Qasrodasht Av, Shiraz, Iran
ُShiraz Iran (Islamic Republic of) +98 71 2340 7746 stud2380082006@sums.ac.ir School of Management and Medical Informatics, Shiraz University of Medical Sciences, Shiraz, Iran scientific Roxana Sharifian
School of Management and Medical Informatics, Almas Building, No 29 Allay, Qasrodasht Av, Shiraz, Iran
shiraz Iran (Islamic Republic of) +98 71 2340 7746 sharifianr@sums.ac.ir School of Management and Medical Informatics, Shiraz University of Medical Sciences, Shiraz, Iran Iran (Islamic Republic of) Iran (Islamic Republic of) Iran (Islamic Republic of) Iran (Islamic Republic of) Iran (Islamic Republic of) Iran (Islamic Republic of) Inclusion criteria: male and female subjects with chronic non-specific low back pain; at the age of 18-55 years old; Having back pain for more than three months without any pathological cause; subjects should not have been any history of other illnesses (such as infection, cancer, inflammatory diseases, osteoporosis) or surgical interventions; back pain confirmed by orthopedic specialist; pain score less than 6 on numeric rating scale for pain (NRS Pain); Moderate disability score (25-50) based on Oswestry Low Back Pain disability questionnaire; internet access; having a smart phone or personal computer or laptop. Exclusion criteria: subjects with regular physical activity with 30 to 45 minutes duration, at least three times per week; subjects with past history of spine and herniation disk surgery; Pain in the spine corroborating fever and chills; morning stiffness; inflammatory diseases and fracture in the spine indicating the presence of osteoporosis; subjects with past history of fractures of vertebrae, pelvis and lower extremities; subjects with Malignancies, rheumatoid arthritis or systemic infectious diseases; subjects who regularly take pain killer medications and anti-inflammatory drugs; pregnancy or less than 6 months postpartum; body mass index of 30 or higher; presence of arthritis. 18 years 55 years Both M54.5 Low back pain Rehabilitation Rehabilitation Intervention group: 5 educational videos will be produced including the stages of exercise and the exercise program will be sent to the intervention group through 12 sessions during 4 weeks (3 sessions per week) based on the treatment protocol. Each session takes 30 to 45 minutes. Each session has been designed in four parts: warm-up, preform exercise programs, cooling, questions and answers. Control group: the control group will not participate in any specific treatment plan and receive only their usual care. Pain intensity. Timepoint: Before the start of interventions and one week after the interventions. Method of measurement: Numeric Rating Scale for Pain (NRS Pain). Clinical indicies of balance. Timepoint: Before the start of interventions and one week after the interventions. Method of measurement: single leg stand test and Star Excursion Balance Test to measure static balance and dynamic balance respectively. Functional Disability. Timepoint: Before the start of interventions and one week after the interventions. Method of measurement: Oswestry Disability Index (ODI). Quality of life. Timepoint: Before the start of interventions and a week after the interventions. Method of measurement: World Health Organization Quality of Life Questionnaire-100(WHOQOL-100). Patient satisfaction. Timepoint: 1 week after completion of the intervention. Method of measurement: questionary. Vice Chancellor for Research of Shiraz University of Medical Sciences Approved 2016-10-09 Ethics Committee of Shiraz University of Medical Sciences Zand Av, The Central Building of Shiraz University of Medical Sciences, Shiraz, Iran Shiraz Iran (Islamic Republic of)