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临床试验/NCT05843136
NCT05843136已完成不适用

Interferential Current Treatment Reduces Low Back Pain and Improves Functionality in Patients With Chronic Low Back Pain.

Universidade Federal do Oeste do Para2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2022年1月5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
24
试验地点
2
主要终点
Isolated comparative evaluation method, before and after, in the three arms with Application of Rolland Morris Questionnaires

研究概览

简要总结

. 24 individuals were evaluated, with low back pain for more than 12 weeks and aged between 12 and 65 years. The current used in the lumbar region of the participants was of the tetrapolar interferential type and the stimulation mode was the automatic vector, carrier of 4,000 HZ, modulation frequency (AMF) of 50 HZ, sweep frequency of SWEEP of 20HZ. The assessment of pain and functionality was performed using the data collection instrument, the Visual Analogue Pain Scale (VAS), Rolland Morris Disability Questionnaire (RMDQ) and the Owestry Disability Questionnaire (ODQ) respectively. The present study demonstrates that treatment with interferential current promotes chemical improvement in participants, which opens up new perspectives on the use of this therapeutic approach.

详细描述

Low back pain is characterized by pain and represents a change in health that affects mainly adults, although electrostimulation represents an important tool in the treatment of patients with chronic nonspecific low back pain, the clinical efficacy of the interferential current used in physiotherapy still lacks reinforcement for clinical validation. In this way, the present study evaluated whether the use of interferential current contributes to reducing chronic low back pain and analyzed whether the electrotherapeutic protocol can benefit the physical functionality of patients with chronic low back pain. 24 individuals were evaluated, with low back pain for more than 12 weeks and aged between 12 and 65 years. The current used in the lumbar region of the participants was of the tetrapolar interferential type and the stimulation mode was the automatic vector, carrier of 4,000 HZ, modulation frequency (AMF) of 50 HZ, sweep frequency of SWEEP of 20HZ. The assessment of pain and functionality was performed using the data collection instrument, the Visual Analogue Pain Scale (VAS), Rolland Morris Disability Questionnaire (RMDQ) and the Owestry Disability Questionnaire (ODQ) respectively. Data analysis was performed using the JAMOVI 2.2.5 software. Our data showed that individuals with interferential current showed significant improvement in pain relief, as well as in the functional pattern of pain improvement. The present study demonstrates that treatment with interferential current promotes chemical improvement in participants, which opens up new perspectives on the use of this therapeutic approach.

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 (Participant)

盲法说明

only the participant was blinded

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Individuals of both genders
  • Aged between 18 and 65 years
  • Voluntarily sought the Clinic's physiotherapy service
  • Low back pain for more than 12 weeks
  • Medical request and diagnosis of low back pain with or without pain radiating to the lower limbs
  • Immunization against COVID
  • Signature of the free detailed term clarified. (FDTC)

排除标准

  • Physiotherapy treatment carried out in a period equal to or less than 8 weeks before starting the research
  • Reporting any contraindications inherent to the use of electrotherapy
  • Participants with fractures or spinal surgery
  • Involved in a legal medical dispute
  • Diagnosis of fibromyalgia
  • Patients with flu-like symptoms during the research period
  • Participants who have more than 2 (two) absences will be excluded from the research.

结局指标

主要结局

Isolated comparative evaluation method, before and after, in the three arms with Application of Rolland Morris Questionnaires

时间窗: 12 months

Application of Rolland Morris Questionnaires before and after intervention, this questionnaires assesses mild and moderate pain and disability

Isolated comparative evaluation method, before and after, in the three arms, Application of Owestry Questionnaire

时间窗: 12 months

Application of Owestry Questionnaire before and after intervention, this questionnaires evaluates more severe disabilities

Isolated comparative evaluation method, before and after, in the three arms, Application analogue visual score for pain

时间窗: 12 months

Application analogue visual score for pain before and after intervention, evaluates the level of pain according to the patient's reference

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

LUIZ PAULO SOBRAL PEREIRA

Master's in Health Sciences

Universidade Federal do Oeste do Para

研究点 (2)

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