Health Condition 1: M990- Segmental and somatic dysfunction
Conditions
Interventions
Intervention1: Experimental Group: Experimental group will receive a wearable device. The device will be monitoring the posture and muscle activity and also provide real time feedback on posture corre
Sponsors
NIL
Eligibility
Inclusion criteria
Inclusion criteria: People between the ages of 18 and 45 years, of both genders, will be included. Individuals who meet the clinical diagnosis of lower cross syndrome will be evaluated through Increased lumbar lordosis, pelvic tilt revealed by posture assessment Iliopsoas tightness identified by Thomas test, and lower back muscle tightness confirmed with the tape measurement method Weakness of abdominal and gluteal muscles estimated through manual muscle testing
Exclusion criteria
Exclusion criteria: History of surgery to the spine, pelvic, and lower limb within the last six months. Any structural spinal deformities, such as Scoliosis, Kyphosis. Neurological conditions (such as stroke, multiple sclerosis, and neuropathies) affecting postural and motor control. Pregnancy Females with any gynaecological disorders. Participation in any other physiotherapy intervention related to posture correction programs in the last four weeks.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| abdominal and gluteal strength will be assessed using manual muscle testing. The Thomas test will be used to evaluate iliopsoas tightness, and the tape measurement method will be used for erector spinae assessment. Pelvic tilt and lumbar hyperlordosis APECS app will be employed.Timepoint: at baseline, after 2 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Public ContactRavia
Chitkara School of Health Sciences, Chitkara University
Outcome results
None listed