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临床试验/CTRI/2024/07/071238
CTRI/2024/07/071238已完成不适用

Effect of Integrated Neuromuscular inhibition technique versus Myofascial induction therapy on trapezius trigger points: A Randomized Clinical Trial

Soumya S K1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2024年8月5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 Pressure Threshold Neck Range of Motion

研究概览

简要总结

TITLE - EFFECT OF INTEGRATED NEUROMUSCULAR INHIBITION TECHNIQUE VERSUS MYOFASCIAL INDUCTION THERAPY ON TRAPEZIUS TRIGGER POINTS: A RANDOMIZED CLINICAL TRIAL

Objective -To compare the effectiveness of the Integrated Neuromuscular Inhibition Technique versus Myofascial Induction therapy on trapezius trigger points by using a Visual analog scale, Neck Disability Index in terms of pain and functional activities, Pain pressure threshold and range of motion using pressure algometer and goniometer.

Inclusion Criteria

• Participants who are willing to participate.

• The study covers participants aged 20 to 40 years.

• Participants with myofascial trigger points confirmed through palpation, exhibiting tenderness in grades 2 and 3.

• Visual analog scale greater than 5.

Exclusion Criteria

• Participants with a history of Neurological disorders, radiculopathy, fibromyalgia, Joint disorders, and fractures.

• Participants on medication.

Outcome measures

  1. Pain Pressure Threshold

  2. Neck Range of Motion

  3. Visual Analog Scale

  4. Neck Disability Index

Procedure

Both groups will receive a Hot pack and Interferential therapy for 15 minutes. before the treatment

Group 1: Participants in Group 1 will receive an Integrated neuromuscular inhibition technique which will be carried out

in 6 sessions over 2 weeks

Group 2 Participants in Group 2 will receive myofascial induction therapy for 6 sessions over 2

weeks.

Home protocol and Postural education will be given

After 6 sessions and 1 month follow up the post intervention is assessed.

The pre-and post-data will be then collected, tabulated, and analyzed

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
None

入排标准

年龄范围
20.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • Participants who are willing to participate.
  • Participants aged 20 to 40 years.
  • Participants with myofascial trigger points confirmed through palpation exhibited tenderness in grades 2 and
  • Visual analog scale greater than or equal to 5.

排除标准

  • Participants with a history of Neurological disorders, radiculopathy, fibromyalgia, Joint disorders, and fractures.
  • Participants on medication.

结局指标

主要结局

Pain Pressure Threshold Neck Range of Motion

时间窗: Pain Pressure Threshold and Neck Range of Motion will be assessed in Baseline, Post-treatment after 6 sessions and after 1 month of follow-up

次要结局

  • Visual analog scale(Neck Disability Index Questionnaire)

研究者

发起方
Soumya S K
申办方类型
Other [Self Sponsored Project]
责任方
Principal Investigator
主要研究者

Soumya S K

KAHER institute of Physiotherapy

研究点 (1)

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