Women with chronic low back pain having children with cerebral palsy. Other soft tissue disorders related to use, overuse and pressure, Unspecified soft tissue disorder related to use, overuse and pressure, Low back pain
Conditions
Interventions
Intervention 1: Control group: the self-care education will be trained and the mothers will be received the booklet. Intervention 2: Experimental group: in addition to self-care education they will be
Control group: the self-care education will be trained and the mothers will be received the booklet
Experimental group: in addition to self-care education they will be received muscle stabilization training for 8 week 3 times per week
Sponsors
Deputy of research and technology of Semnan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Having a child with cerebral palsy; mother was the primary caregiver for children with cerebral palsy; having low back pain for at least three months Exclusion criteria: a history of trauma in low back; reported the history of vertebral column fractures and hip fractures; report any neurological diseases such as multiple sclerosis, Parkinson's, etc.; report systemic diseases such as diabetes or Rheumatoid arthritis, tuberculosis, etc.; scoliosis and kyphosis of vertebral column and report any signs of serious disease in spinal included: Non-mechanical pain (without regard to time or activity); chest pain, wide paresthesia in the limbs, severe muscle weakness in lower limb, unexplained weight loss, fever, history of recently surgery, previous history of carcinoma, reported human immunodeficiency virus infection and substance abuse
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Muscle activities. Timepoint: Before intervention, after 8 weeks intervention and 4 weeks after the end of intervention. Method of measurement: Ultrasonography.;Disability. Timepoint: Before intervention, after 8 weeks intervention and 4 weeks after the end of intervention. Method of measurement: Roland-Morris Questionnaire.;Pain. Timepoint: Before intervention, after 8 weeks intervention and 4 weeks after the end of intervention. Method of measurement: Visual Analogue Scale for pain. | — |
Secondary
| Measure | Time frame |
|---|---|
| Depression. Timepoint: Before intervention, after 8 weeks intervention and 4 weeks after the end of intervention. Method of measurement: Beck depression questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Ahmadizadeh
Semnan University of Medical Sciences
Outcome results
None listed