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Clinical Trials/NCT02088463
NCT02088463
Completed
Not Applicable

Efficacy of Lumbar Mobilization on Postpartum Low Back Pain in Egyptian Females: A Randomized Control Trial

Cairo University1 site in 1 country45 target enrollmentDecember 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain, Mechanical
Sponsor
Cairo University
Enrollment
45
Locations
1
Primary Endpoint
Pain intensity
Status
Completed
Last Updated
10 years ago

Overview

Brief 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.

Detailed 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

Registry
clinicaltrials.gov
Start Date
December 2012
End Date
October 2013
Last Updated
10 years ago
Study Type
Interventional
Study Design
Factorial
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Dalia Mohamed Kame

Associate Professor of Physical Therapy

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Females with LBP lasting more than 3 months since their delivery
  • their age range 25-35 years old with body mass index (BMI) less than 30kg/m2

Exclusion Criteria

  • medical conditions that don't allow the subject to lie prone comfortably as, cardiovascular disease, uncontrolled hypertension, abdominal hernia, severe respiratory diseases, as well as problems in the back e.g. previous low back surgery, spinal malignancy. In addition to known rheumatic joint disease, and upper or lower motor neuron lesion that affects lower limbs

Outcomes

Primary Outcomes

Pain intensity

Time Frame: after 4 weeks from starting the intervention

each case assessed two times pre- post intervention, intervention was lasted for 4 weeks

functional disability

Time Frame: after 4 weeks from starting the intervention

each case assessed two times pre-post intervention, intervention lasted for 4 weeks

back muscle activity

Time Frame: after 4 weeks from starting the intervention

each case assessed two time pre- post intervention, intervention lasted for 4 weeks

Study Sites (1)

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