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临床试验/NCT07037329
NCT07037329进行中(未招募)不适用

To Determine the Effectiveness of TENS vs EMS on Hemodynamics Parameters of Hypertension

Superior University1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2025年3月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
42
试验地点
1
主要终点
SF-36 Health Survey (Optional for Quality of Life)

研究概览

简要总结

This study aimed to evaluate the comparative effectiveness of Transcutaneous Electrical Nerve Stimulation (TENS) and Electrical Muscle Stimulation (EMS) on hemodynamic parameters in patients with hypertension. A total of 42 hypertensive patients were randomly divided into two equal groups: Group A received TENS, and Group B received EMS, over a period of four weeks. Pre- and post-treatment measurements of systolic blood pressure (SBP), diastolic blood pressure (DBP), and heart rate (HR) were recorded. Results showed that both TENS and EMS produced significant improvements in all parameters within their respective groups.

详细描述

However, the TENS group demonstrated a greater reduction in SBP and DBP, while the EMS group showed better improvement in heart rate control. The findings suggest that both treatments are effective non-pharmacological options for managing hypertension, with TENS being more effective overall in lowering blood pressure. These modalities may offer supportive benefits in long-term hypertension management strategies.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
25 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •(25-60 years) including both male and female
  • •Patients clinically diagnosed with primary (essential) hypertension.
  • •Blood pressure ranging from 140/90 mmHg to 160/100 mmHg (Stage 1 to early Stage 2 hypertension).
  • •Participants who are not currently on intensive antihypertensive therapy or are on a stable dose of medication.
  • •Willingness to participate voluntarily and provide written informed consent.
  • •Patients who are not involved in any physical activity.
  • •Participants who are overweight according to normal BMI.

排除标准

  • •Secondary hypertension due to renal, endocrine, or other systemic causes. Individuals with pacemakers, implanted defibrillators, or other electronic medical devices.
  • •Patients with severe cardiovascular conditions, such as recent myocardial infarction, heart failure, or arrhythmias.
  • •History of seizure disorders or epilepsy. Cancer Patients
  • •Presence of skin lesions, open wounds, or infections at the site of electrode placement.
  • •Patients undergoing physiotherapy or electrical therapy elsewhere during the study period.
  • •Individuals with known neurological or musculoskeletal disorders that could interfere with EMS or TENS effectiveness

研究组 & 干预措施

Transcutaneous Electrical Nerve Stimulation (TENS)

Experimental

干预措施: Transcutaneous Electrical Nerve Stimulation (TENS) (Diagnostic Test)

Electrical Muscle Stimulation (EMS)

Experimental

干预措施: Electrical Muscle Stimulation (EMS) (Diagnostic Test)

结局指标

主要结局

SF-36 Health Survey (Optional for Quality of Life)

时间窗: 6 Month

Measures general health status and quality of life 36 items grouped into 8 domains (e.g., physical functioning, general health) Each domain scored from 0 (worst) to 100 (best)

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

Muhammad Naveed Babur

Principal Investigator

Superior University

研究点 (1)

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