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临床试验/NCT07425301
NCT07425301已完成不适用

Comparing the Effects of Ischemic Compression and Kinesiology Taping Techniques in Patients With Chronic Low Back Pain

Hasan Kalyoncu University1 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2024年11月3日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
102
试验地点
1
主要终点
Change in Pain Intensity (Visual Analog Scale)

研究概览

简要总结

This study evaluates the effects of ischemic compression and kinesiology taping techniques on pain intensity and lumbar range of motion in individuals with chronic low back pain. Participants are assigned to one of three groups: a conventional treatment group, a conventional treatment plus kinesiology taping group, or a conventional treatment plus ischemic compression group. Interventions are administered over a three-week period. Outcome measures are assessed before and after the intervention using standardized assessment methods. The purpose is to compare changes among groups and examine the effects of adding these techniques to conventional treatment.

详细描述

Chronic low back pain is a common musculoskeletal condition associated with pain, reduced mobility, and functional limitations. Nonpharmacological interventions are frequently used to support symptom management and improve physical function. Manual therapy techniques and supportive therapeutic applications are commonly included in rehabilitation programs for individuals with chronic low back pain.

This study is designed to investigate the effects of ischemic compression and kinesiology taping techniques in individuals with chronic low back pain. Participants are assigned to different intervention groups receiving either conventional treatment alone or conventional treatment combined with additional therapeutic techniques. Interventions are delivered according to structured protocols over a defined treatment period. Outcome measures evaluate changes in pain intensity and lumbar range of motion using standardized assessment methods.

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
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Volunteers willing to participate in the study,
  • Those who have had back pain for at least 12 weeks,
  • Those who have been tested with a test patch and have no allergy to kinesiology tape,
  • Patients who can comply with the exercise programme to be applied were included in the study.

排除标准

  • Patients who have undergone surgery for back pain,
  • Pregnant women,
  • Patients with rheumatological diseases were not included in the study.

研究组 & 干预措施

Conventional Treatment Group

Active Comparator

Participants in this group receive conventional treatment consisting of standard physiotherapy modalities administered according to a structured treatment protocol over a three-week period. No additional taping or manual compression techniques are applied in this group.

干预措施: Conventional Physiotherapy Program (Other)

Conventional Treatment Plus Kinesiology Taping Group

Experimental

Participants in this group receive conventional treatment consisting of standard physiotherapy modalities together with kinesiology taping applied according to a structured application protocol over a three-week treatment period.

干预措施: Kinesiology Taping (Procedure)

Conventional Treatment Plus Ischemic Compression Group

Experimental

Participants in this group receive conventional treatment consisting of standard physiotherapy modalities together with ischemic compression therapy applied according to a structured protocol during scheduled sessions over a three-week period.

干预措施: Ischemic Compression Therapy (Procedure)

结局指标

主要结局

Change in Pain Intensity (Visual Analog Scale)

时间窗: Baseline and after completion of the 3-week intervention period

Pain intensity is assessed using the Visual Analog Scale, a validated measure consisting of a scale ranging from no pain to worst imaginable pain. Change is calculated as the difference between pre-intervention and post-intervention scores.

次要结局

  • Change in Lumbar Flexion Range of Motion(Baseline and after completion of the 3-week intervention period)
  • Change in Lumbar Extension Range of Motion(Baseline and after completion of the 3-week intervention period)
  • Change in Lumbar Right Lateral Flexion Range of Motion(Baseline and after completion of the 3-week intervention period)
  • Change in Lumbar Left Lateral Flexion Range of Motion(Baseline and after completion of the 3-week intervention period)

研究者

发起方
Hasan Kalyoncu University
申办方类型
Other
责任方
Principal Investigator
主要研究者

İlker DEMİR

Inonu Universty

Hasan Kalyoncu University

研究点 (1)

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