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临床试验/NCT02088463
NCT02088463已完成不适用

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

Cairo University1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2012年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
45
试验地点
1
主要终点
Pain intensity

研究概览

简要总结

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.

详细描述

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

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
25 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •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

排除标准

  • •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

研究组 & 干预措施

Mobilization (manual therapy)

Experimental

Mobilization (manual therapy) posterior- anterior at the L3 for 2 minutes in addition to the traditional treatment in the form of infra-red and ultrasound. The treatment duration for the three groups was 3 times/week for 4 weeks.

干预措施: mobilization (manual therapy) (Procedure)

Mobilization (manual therapy)

Experimental

Mobilization (manual therapy) posterior- anterior at the L3 for 2 minutes in addition to the traditional treatment in the form of infra-red and ultrasound. The treatment duration for the three groups was 3 times/week for 4 weeks.

干预措施: Ultrasound and infrared devices (Device)

placebo mobilization

Placebo Comparator

placebo mobilization applied without force application. The treatment duration for the three groups was 3 times/week for 4 weeks

干预措施: Placebo mobilization (Procedure)

placebo mobilization

Placebo Comparator

placebo mobilization applied without force application. The treatment duration for the three groups was 3 times/week for 4 weeks

干预措施: Ultrasound and infrared devices (Device)

Ultrasound and infrared therapy

Other

ultrasound and infrared are a traditional treatment for low back painThe treatment duration for the three groups was 3 times/week for 4 weeks.

干预措施: Ultrasound and infrared devices (Device)

结局指标

主要结局

Pain intensity

时间窗: after 4 weeks from starting the intervention

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

functional disability

时间窗: after 4 weeks from starting the intervention

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

back muscle activity

时间窗: after 4 weeks from starting the intervention

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

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Dalia Mohamed Kame

Associate Professor of Physical Therapy

Cairo University

研究点 (1)

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