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临床试验/NCT06461507
NCT06461507已完成不适用

Effects of Jandas's Approach With and Without Post Isometric Relaxation Technique on Pain, Muscle Flexibility, Functional Disability in Patients With Posterior Lower Crossed Syndrome

Riphah International University2 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2024年6月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
38
试验地点
2
主要终点
Numerical pain rating scale (NPRS)

研究概览

简要总结

Posterior lower crossed syndrome is a perplexing puzzle of muscular imbalance, manifests as an intricate interplay between weakened glutes and tight flexors. The aim of the study will be to determine the effects of Jandas's approach with and without post-isometric relaxation technique on pain, muscle flexibility, and functional disability in patients with the posterior lower crossed syndrome.

详细描述

A Randomized Controlled Trial will be conducted at physical therapy department of Rabia Welfare Hospital Lahore, FMH Physiotherapy Clinic Lahore and Shafaeen Physiotherapy Clinic Lahore through convenient sampling technique on 30 patients which will be allocated using simple random sampling through sealed opaque enveloped into Group A and Group B. Group A will be treated with janda's approach and Group B will be treated with combination of post isometric relaxation technique for Illiopsoas and janda's approach at the frequency of 3 sets with 10 repetitions and twice a week. Outcome measures will be conducted through pain,muscle flexibility, pelvic tilt and disability questionnaire after 4 weeks. Data will be analysed using SPSS software version 25.After assessing normality of data by Shapiro-wilk test, it will be decided either parametric or nonparametric test will be used within a group or between two groups.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age:20-60 years
  • Gender: Both males and females
  • NPRS (Numerical Pain Rating Scale): < 7
  • Positive Finger to Floor Test : > 48cm in males, >50cm for females
  • Positive Modified Thomas Test: greater than zero
  • Patients with anterior pelvic tilt

排除标准

  • Preexisting spinal pathology
  • Congenital abnormality
  • Neurological deficits,
  • Recent spinal or lower-limb trauma or surgery
  • Spasm of the trunk or lower-limb muscles
  • Lower-limb radiculopathy
  • Pregnancy

结局指标

主要结局

Numerical pain rating scale (NPRS)

时间窗: upto 4 weeks

o Changes from base Line Numeric Pain rating scale is a scale for pain starting from 0-10. where 0 indicate no pain and 10 indicate severe pain. The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain).

Modified Thomas Test- Muscle flexibility test

时间窗: upto 4 weeks

* Have the patient lie supine on a firm surface, with their legs straight. * Place your hand under the patient's lower back to maintain a neutral spine. * Slowly flex the patient's hip, bringing their knee towards their chest, until their thigh is perpendicular to the table. * Assist the patient in flexing their hip further, keeping their knee bent at a 90-degree angle. * Measure the angle between the patient's thigh and the table using a goniometer or inclinometer. * Compare the measurement to the normal range (usually around 15-20 degrees) to determine if there is a restriction in iliopsoas flexibility.

Finger to floor test -Muscle flexibility test

时间窗: upto 4 weeks

* The patient is asked to bend forward and attempt to reach for the floor with their fingertips. * The physical therapist then measures the distance between the patient's right long finger and the floor using a standard measuring tape * Ask the client whether pain, stiffness or both limit the movement(Fingertips to floor (FTF) test). * If the FTF test is limited by pain, the location and pain score out of 10 should be documented. * If the FTF test is 0 cm or the patient is able to place their palms to the floor with no pain, a different outcome measure should be considered.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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