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NCT07037329Active, not recruiting

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

Source: ClinicalTrials.gov · Last updated 25 Jun 2025

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
42 (actual)
First submitted
17 Jun 2025
Start date
4 Mar 2025
Primary completion date
1 Jun 2025
Lead sponsor
Superior University
NCT number
NCT07037329

What you commit to

  • Study type: Interventional
  • Participants enrolled: 42
  • From 4 Mar 2025 to the primary completion date, 1 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients undergoing physiotherapy or electrical therapy elsewhere during the study period.

Other illness

  • 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.
  • Individuals with known neurological or musculoskeletal disorders that could interfere with EMS or TENS effectiveness

Who the study is looking for

  • (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.

Age in the registry: 25 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Yasin Poly Clinic, Behria town Lahore
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.