low back pain. Low back pain
Conditions
Interventions
Intervention 1: Prescribtion of an abdomino lumbo pelvic belt in group1 of trial with educational pamphlete consists of usual care in prevention and treatment of low back pain in pregnancy for 6 week
Treatment - Other
Rehabilitation
Lifestyle
Prescribtion of an abdomino lumbo pelvic belt in group1 of trial with educational pamphlete consists of usual care in prevention and treatment of low back pain in pregnancy for 6 weeks.
Exercise prescribtion in group 2 of trial consist of stretching and strenghtening of abomen, lumbar and pelvic muscles and core stability exercises with one booklet consists of guidelines for these e
An educational pamphlete in control group consists of usual care for treatment and prevention of low back pain in pregnancy for 6 weeks.
Sponsors
Research Deputy of Tehran University of Medical Sciences and Health Services
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Inclusion criteria: 1- Healthy pregnant women with pain in lumbar region. 2- Pregnancy age: 20-32 weeks of pregnancy. 3- The consent will be received from all participants. 4- Mono fetus pregnancy. 5- Pelvic girdle pain had been diagnosed with history, physical examination and specific tests. 6- Contraindications of exercise in pregnancy should not be existed in participants such as: vaginal bleeding, preeclampsia, IURG, placenta previa, preterm labor, cervix insufficiency, rupture of membrane in recent pregnancy. 7- Systemic diseases should not be existed in participants such as: restrictive lung diseases, heart diseases. Exclusion criteria: 1- If contraindications of exercise in pregnancy happened during study. 2- If participants don’t refer after 3 and 6 weeks of intervention. 3- If participants don’t use belt and exercise regularely.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Back pain. Timepoint: 3 and 6 weeks after interventions. Method of measurement: Visual Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life. Timepoint: 3 and 6 weeks after interventions. Method of measurement: WHO quality of life questionnaire.;Patient's ability in implementation of daily activities. Timepoint: 3 and 6 weeks after interventions. Method of measurement: OSWESTRY disability questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Abolhasani
Sports medicine research center.
Outcome results
None listed