Sacroiliac joint dysfunction. Sprain of sacroiliac joint
Conditions
Interventions
Intervention 1: Intervention group: Lumbo-pelvic core stability exercises along with muscle energy technique. Intervention 2: Control group: Muscle energy technique.
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Age range 18-45 years Having literacy (at least a diploma for neuro-cognitive variables) Having a unilateral disorder of AIR and PIR The direction of the disorder side and the painful side are the same Pain below the fifth lumbar vertebra (L5) and around the PSIS Chronic pain that has lasted for at least 3 months Minimum pain intensity based on VAS should be 30 The minimum degree of disability based on ODI should be 30% Body mass index between 18-28 kg/m2 The positivity of 3 out of 5 iliac crest height tests, the level of PSISs, the level of ASISs, Standing Flexion Test and Gillet's Test, the positivity of Long Sitting Test and the positivity of 3 out of 5 tests Distraction Test, Compression Test, Thigh thrust test, sacral thrust test and Gaenslen's test The minimum intensity of the disturbance in performing the Active Straight Leg Raise movement should be 3
Exclusion criteria
Exclusion criteria: Radiculopathy Fractures of the spine and lower limbs Lumbosacral surgery Spinal deformity and scoliosis Anatomical leg length difference with a difference of more than 1 cm pregnancy Rheumatoid arthritis and ankylosing spondylitis Malignancies Infection Cardiovascular disease and pacemakers The subject's unwillingness to cooperate in the beginning or continuation of the sessions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain: To measure the pain of patients, a 100 mm long ruler known as Visual Analogue Scale will be used, with the word "no pain" at one end and the word "maximum pain" at the other end. In this study, people who have pain of at least 30 will be included in the study. Timepoint: Before the start of the intervention, immediately after the first intervention session, after the 6th intervention session and one month after the last intervention session. Method of measurement: Visual Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Neuro-cognitive variables that include visual and auditory selective reaction time and complex visual and complex auditory choice and prediction skill at low and high speed, which are measured with the Speed ??Anticipation Reaction Time system. Timepoint: Before the first intervention, immediately after the first internal session, after the 6th intervention session and one month after the last intervention session. Method of measurement: Speed ??Anticipation Reaction Time system. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Azadeh Shadmehr
Tehran University of Medical Sciences
Outcome results
None listed