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临床试验/NCT07744451
NCT07744451已完成不适用

A Comparison of the Efficiency of Physiotherapy and Kinesiotaping Treatments in the Treatment of Post-Covid-19 Back Pain

Medipol University1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2021年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
33
试验地点
1
主要终点
Pain Intensity assessed by Visual Analogue Scale (VAS)

研究概览

简要总结

Objective:

This study aims to compare and evaluate the effectiveness of kinesiotaping and traditional physiotherapy methods, which are frequently used in the treatment of musculoskeletal diseases, on mid-back pain (MBP) developed after COVID-19.

Study Design and Methods:

Patients aged 18 or older who have been diagnosed with COVID-19, have completed their medical treatment, and whose isolation period has ended are included in the study. The patients' age, sex, and body mass index (BMI) are recorded.

The participants are assigned to receive one of two interventions. In the first group, kinesiotapes are applied and left on the patient's back for a total of 10 days. The second group is treated with traditional physiotherapy methods, specifically Vacuum Interferential Current Therapy and Hot Pack Therapy.

Clinical evaluations are performed using the Visual Analogue Scale (VAS), Pain Quality Assessment Scale, LANSS Neuropathic Pain Scale, and Nottingham Extended Activities of Daily Living Index. Measurements are taken at two time points: baseline (pre-treatment) and at the end of the 10th day (post-treatment).,

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
Single (Outcomes Assessor)

盲法说明

To minimize bias, the researcher who performed the baseline and post-treatment clinical assessments (VAS, NEADLS, LANSS) was blinded to the patients' group allocations.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged 18 years and older.
  • Patients experiencing mechanical mid-back pain (MBP) that developed after recovering from a confirmed COVID-19 infection.
  • Volunteering to participate in the study and providing written informed consent.

排除标准

  • History of previous spinal surgery or spinal trauma.
  • Presence of structural spinal deformities (e.g., severe kyphosis or scoliosis).
  • Presence of radicular pain, neurological deficits, or suspected disc herniation.
  • Active infection, malignancy, or severe systemic inflammatory diseases.
  • Known skin allergy or dermatological conditions preventing the application of Kinesio Tape.
  • Pregnancy.

结局指标

主要结局

Pain Intensity assessed by Visual Analogue Scale (VAS)

时间窗: Baseline (Pre-treatment) and Day 10 (Post-treatment)

The Visual Analogue Scale (VAS) is used to evaluate the patient's mid-back pain intensity under three conditions: at rest, at night, and during activity/exercise. The scale is a 10 cm line where 0 represents "no pain" and 10 represents "the worst imaginable pain." Higher scores indicate greater pain severity.

次要结局

未报告次要终点

研究者

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

Çağlayan Aslanbaş

Asst. Prof. Dr.

Medipol University

研究点 (1)

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