The effect of exercise and taping on low back pain of pregnant wome

Phase 2

• Conditions: Condition 1: low back pain. Condition 2: disability caused by low back pain.; Loin painLow back strainLumbago NOS; Limitation of activities due to disability; M54.5 Low

• Registration Number: IRCT2015070223021N1
• Lead Sponsor: Vice Chancellor for research of Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 90

Inclusion Criteria

Written consents should be completed; should be the resident of mashhad; should have the ability to read and write
; having the age of pregnancy from 16 to 22 weeks; the intensity score of low back pain should be between 50 and 100 according to Quebec back pain questionnaire; the disability score caused by low back pain should be between 10 to 50 based on the Oswestry questionnaire; The BMI should be from 19.8 to 26; Maternal height should be 150 cm or more; The exercise group should have health certificate of heart and lung; should not have a medical condition; Should not have regular exercise during current pregnancy; Should not have a high risk pregnancy; Should not have the history of low back pain before pregnancy; should not have spinal column disorder; should not have pregnancy following assisted reproductive techniques; Do not have allergy to the glue; Do not have rectus dyastasis ; Do not have systolic blood pressure> 140 mm Hg and diastolic pressure >90 mm Hg ; No other specific method for pain relief.
Exclusion criteria:
Any problem or particular disease during the study; use alternative methods to relieve pain; The sensitivity to the glue during the study; Did not exercise two days of a week ; Did not exercise according to the training protocol; Did not present two session in order to devise type; If the type separate automatically did not refer to devise type before one week.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Disability caused by low back pain. Timepoint: Before the intervention, then every week for six weeks. Method of measurement: Oswestry functional disability questionnaire.;Back pain. Timepoint: Before the intervention, then every week for six weeks. Method of measurement: Quebec Back Pain questionnaire.

Secondary Outcome Measures

Name	Time	Method
umbar lordosis. Timepoint: Before the intervention and after six weeks. Method of measurement: Flexible ruler.