To Determine the Effectiveness of TENS vs EMS on Hemodynamics Parameters of Hypertension
NCT ID: NCT07037329
Last Updated: 2025-06-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
42 participants
INTERVENTIONAL
2025-03-04
2025-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Transcutaneous Electrical Nerve Stimulation (TENS)
Transcutaneous Electrical Nerve Stimulation (TENS)
TENS is a non-invasive electrotherapy technique used to manage pain and modulate physiological responses such as blood pressure. In this study, patients in Group 1 received TENS therapy as the primary intervention.
Electrical Muscle Stimulation (EMS)
Electrical Muscle Stimulation (EMS)
EMS is a form of electrotherapy that causes muscle contractions through electrical impulses delivered via surface electrodes. In this study, patients in Group 2 received EMS therapy to investigate its effect on hemodynamic parameters in individuals with hypertension.
Interventions
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Transcutaneous Electrical Nerve Stimulation (TENS)
TENS is a non-invasive electrotherapy technique used to manage pain and modulate physiological responses such as blood pressure. In this study, patients in Group 1 received TENS therapy as the primary intervention.
Electrical Muscle Stimulation (EMS)
EMS is a form of electrotherapy that causes muscle contractions through electrical impulses delivered via surface electrodes. In this study, patients in Group 2 received EMS therapy to investigate its effect on hemodynamic parameters in individuals with hypertension.
Eligibility Criteria
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Inclusion Criteria
* 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.
Exclusion Criteria
* 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
25 Years
60 Years
ALL
No
Sponsors
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Superior University
OTHER
Responsible Party
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Muhammad Naveed Babur
Principal Investigator
Locations
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Yasin Poly Clinic, Behria town Lahore
Lahore, , Pakistan
Countries
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Other Identifiers
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DPT/Batch-Fall20/1012
Identifier Type: -
Identifier Source: org_study_id
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