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临床试验/NCT06988241
NCT06988241已完成不适用

Efficacy of Positional Release Muscles for Neck Pain During Lactation

Kafrelsheikh University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年5月23日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
2
主要终点
Intensity of neck pain

研究概览

简要总结

Purpose of the study: To determine the efficacy of neck muscles positional release for Neck Pain during lactation.Methods:Fifty patient with postpartum neck pain will be recruited. Patients will be randomly assigned into two groups, group A and group B . Patients in both groups will receive posture correction advices during lactation and posture correction exercises but group A will receive additional positional release for upper trapezius. All patients will be evaluated for Pressure pain threshold (PPT) of upper trapezius by algometry, neck disability using Arabic version of neck disability index, pain intensity using 11-numerical rating scale.

详细描述

Treatment procedure Both groups will receive posture education advices during lactation and Posture correction exercise program which will include Strengthening Exercise Program and Spinal Stretches.Spinal stretches were also included .In the intervention program mothers who underwent normal delivery were advised to start home based exercise program after 5 weeks and the caesarean mothers after 2 months of delivery Group (A): will receive Positional release of neck muscles in addition to Posture correction.Positional release technique For deactivation of Trigger Points (TrPs) and decrease spasm Manual approaches. [PRT] was developed by Lawrence H. PRT is a method in which muscles are placed in a position of greatest comfort, and this causes normalization of muscle hypertonicity and fascial tension. Also, it decreases joint hypomobility, increases circulation, followed by a reduction in swelling, decreased pain, and increase muscle strength. The practical section of the study will be undertaken in 4 weeks (3 sessions a week). Measurement will be taken before the start of treatment program then after the end of 4 weeks treatment program.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • lactating mothers.
  • Age between 25-35 years old.
  • six weeks to one year after childbirth.
  • at least a moderate level of education.

排除标准

  • Mothers were excluded if they had facet joint, neurological, or cardio vascular and respiratory conditions.
  • History of breast cancer.

结局指标

主要结局

Intensity of neck pain

时间窗: baseline and four weeks

Neck pain intensity will be measured by 11- numerical rating scale.Primary outcome updated to pain intensity to better reflect the study objective.

Intensity of neck pain

时间窗: baseline and four weeks

Neck pain intensity will be measured by 11- numerical rating scale.Primary outcome updated to pain intensity to better reflect the study objective.

次要结局

  • Pressure pain threshold (PPT)(baseline and four weeks)
  • functional status related to neck disability(baseline and four weeks)
  • Pressure pain threshold (PPT)(baseline and four weeks)
  • functional status related to neck disability(baseline and four weeks)

研究者

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

Norhan Hassan Elsayed

Physical Therapist

Kafrelsheikh University

研究点 (2)

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