Low back pain. Low back strain
Conditions
Interventions
Intervention 1: Acupressure intervention will be done on the main points GB30, BL32, BL60, K1, GV20, H7 for 2 minutes on each of the points, by the researcher, 9 sessions for 3 weeks and 3 times per w
Treatment - Other
Placebo
Acupressure intervention will be done on the main points GB30, BL32, BL60, K1, GV20, H7 for 2 minutes on each of the points, by the researcher, 9 sessions for 3 weeks and 3 times per week in experimen
Intervention in the sham group carried out by the researcher for 2 minutes on each of the points, 3 times a week for three weeks, with the difference that points of pressure one to one and a half cen
Sponsors
Deputy Of Research Of Esfahan University Of Medical Sciences
Eligibility
Sex/Gender
Female
Age
25 Years to 55 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria included nurses desire to take part and placed randomly in three groups, aged 25-55 years, take at least 4 scour according to VAS criteria before the intervention, experience nonspecific low back pain continuously for more than three months based on the detection neurosurgeon, absence of severe pain need immediate treatment or surgery, any open wound, being during menstruation and pregnancy, physical pain, such as rheumatic arthritis, autoimmune diseases, addiction and depression. Exclusion criteria included lack of desire to continue, absence of samples from one sessions, use of other methods of complementary medicine, develop other diseases of the lumbar and Serious physical and mental damage
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Before the intervention, immediately after intervention, 2 weeks and 4 weeks after intervention. Method of measurement: VAS Scale.;Quality Of Life. Timepoint: Before the intervention, immediately after intervention, 2 weeks and 4 weeks after intervention. Method of measurement: SF36. | — |
Secondary
| Measure | Time frame |
|---|---|
| Fatigue. Timepoint: Before the intervention, immediately after intervention, 2 weeks and 4 weeks after intervention. Method of measurement: FSS questionnaire.;Quality of sleep. Timepoint: Before the intervention, immediately after intervention, 2 weeks and 4 weeks after intervention. Method of measurement: Pittsburgh questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam movahedi
Esfahan University of Medical Sciences
Outcome results
None listed