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The self-care education and stabilizing exercise in pain, disability and muscle activities in mothers with chronic low back pain having children with cerebral palsy

Not Applicable
Conditions
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
M70.8, M70
Registration Number
IRCT2015041121686N1
Lead Sponsor
Deputy of research and technology of Semnan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
60
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

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
Depression. Timepoint: Before intervention, after 8 weeks intervention and 4 weeks after the end of intervention. Method of measurement: Beck depression questionnaire.
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