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Clinical Trial Summary

The study was conducted to the following purposes

1. To investigate the effect of lumbar mobilization on muscle activity in postpartum mechanical low back pain.

2. To investigate the effect of lumbar mobilization on pain intensity in postpartum mechanical low back pain patients.

3. To investigate the effect lumbar mobilization on functional disability in postpartum mechanical low back pain patients.

4. To compare between the effects of lumbar mobilization, tactile stimulation (placebo treatment) and traditional treatment in postpartum mechanical low back pain patients.


Clinical Trial Description

all participants divided randomly into three groups, Group A (Study group) received PA lumbar mobilization plus traditional treatment which consisted of Ultrasonic and Infra-red. Group B (Placebo group) received placebo mobilization plus traditional treatment. Group C (Control group) received traditional treatment only ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02088463
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase N/A
Start date December 2012
Completion date October 2013

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