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临床试验/CTRI/2024/10/075082
CTRI/2024/10/075082已完成不适用

Comparing The Effectiveness Of Neural Mobilization And Kinetic Chain Activation Technique Combined With Blood Flow Restriction Training On Pain, ROM, Grip Strength And Functional Disability In Cervical Radiculopathy- A Randomized Clinical Trial

KLE Academy of Higher Education and Research Center1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2024年10月15日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
36
试验地点
1
主要终点
Pain using Numeric Pain Rating Scale, functional disability using Neck Disability Index Scale, grip strength using handheld dynamometer, ROM using goniometer

研究概览

简要总结

COMPARING THE EFFECTIVENESS OF NEURAL MOBILIZATION AND KINETIC CHAIN ACTIVATION TECHNIQUE COMBINED WITH BLOOD FLOW RESTRICTION TRAINING ON PAIN, ROM, GRIP STRENGTH AND FUNCTIONAL DISABILITY IN CERVICAL RADICULOPATHY- A RANDOMIZED CLINICAL TRIAL

Aim of the study-To determine and compare the effectiveness of neural mobilization and KCAT combined with BFR training in cervical radiculopathy.

Inclusion criteria: Participants-

Between age group 18-60.Presence of unilateral symptoms of arm pain, paraesthesia or numbness in the upper limb.Participants’ positive for at least one of the following clinical tests: upper limb nerve tension test (ULNTT), Spurling test and Distraction test. Pain intensity greater than 3/10 on the NPRS

Exclusion criteria: Paricipants-

Patients with previous cervical surgeries and having traumatic history like cervical fractures ,  dislocation, whiplash injuries..History of carcinoma.Neurological deficits like stroke, SCI, PNI, myelopathy, MS.Skin disorders like open wounds, active infection,  allergic conditions

Outcome Measures: NPRS, NDI,Handheld dynamometer, Goniometer

ProcedureParticipants will be divided into two groups. Group A will be given BFR and neural mobilization and group B will be given BFR and KCAT. Participants will be given 5 sessions on alternate days for 2 weeks. Participants will be assessed pre and post intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Participants positive for at least one of the following clinical tests: upper limb nerve tension test (ULNTT), Spurling test and Distraction test Pain intensity greater than 3/10 on the NPRS.

排除标准

  • Patients with previous cervical surgeries and having traumatic history like cervical fractures, dislocation, whiplash injuries History of carcinoma Neurological deficits like stroke, SCI, PNI, myelopathy, multiple sclerosis.

结局指标

主要结局

Pain using Numeric Pain Rating Scale, functional disability using Neck Disability Index Scale, grip strength using handheld dynamometer, ROM using goniometer

时间窗: Outcome will be assessed at baseline and 2 weeks

次要结局

未报告次要终点

研究者

发起方
KLE Academy of Higher Education and Research Center
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Smruti Keskar

KAHER Institute of Physiotherapy

研究点 (1)

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