Actively Recruiting
Effect of Combined Transcutaneous Electrical Stimulation and Isometric Exercise on Peripheral Hemodynamic Parameters in Patients With Resistant Hypertension
Led by Mohamed Mohamed Ali Morgan · Updated on 2026-02-03
50
Participants Needed
1
Research Sites
1 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating whether combining transcutaneous electrical nerve stimulation (TENS) with isometric exercise (IE) can improve blood pressure in adults aged 50 to 60 who have resistant hypertension. This condition involves blood pressure that remains high despite taking three or more different blood pressure medications at maximum doses. The study aims to understand the effect of this combined approach on various blood pressure and heart function measures compared to conventional physical therapy. Participants will be randomly assigned to one of two groups. The experimental group will receive TENS applied to the upper thoracic spine three times a week for 30 minutes per session, alongside isometric handgrip exercises performed with a dynamometer at 30% of maximum effort, repeated four times per session, also three times weekly, for eight weeks. The control group will follow a conventional physical therapy program including aerobic brisk walking, dynamic resistance weight training, stretching, breathing exercises, and lifestyle advice, also three times per week for eight weeks. Throughout the study, participants will be monitored with heart rate and blood pressure measurements before sessions to ensure safety. Researchers will assess blood pressure parameters including systolic, diastolic, mean arterial pressure, pulse pressure, and heart rate variability over the eight-week period. Secondary measures will include oxygen saturation, quality of life, and functional capacity. The study lasts eight weeks, with treatments and assessments conducted regularly to evaluate the effects of the interventions on resistant hypertension.
CONDITIONS
Brief Title
Effect of Electrical Stimulation and Exercise on Blood Flow in Patients With Resistant High Blood Pressure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 50 and 60 years, both men and women included
- Diagnosed with hypertension for at least 5 years
- Resistant hypertension defined as systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg despite three or more antihypertensive medications including a diuretic, or controlled blood pressure on four or more medications
- Body Mass Index (BMI) between 25 and 34.9 kg/m²
- Increased waist circumference: greater than 102 cm for males, greater than 88 cm for females
You will not qualify if you...
- Secondary hypertension due to identifiable causes such as renal artery stenosis, primary aldosteronism, or pheochromocytoma
- History of major cardiovascular events in the last 6 months, including heart attack, stroke, or heart failure worsening
- Severe musculoskeletal or neurological disorders impairing safe performance of isometric exercise
- Contraindications to TENS including implanted electronic devices, uncontrolled arrhythmias, severe skin conditions, peripheral neuropathy, or sensory loss
- Known cognitive impairment or psychiatric conditions limiting ability to follow instructions or give consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 8 weeks
Participants receive either a combined intervention of Transcutaneous Electrical Nerve Stimulation (TENS) and isometric exercises or a conventional physical therapy program including aerobic, dynamic resistance, stretching, and breathing exercises along with lifestyle advice.
3 sessions per week
Trial Site Locations
Total: 1 location
1
Out Clinics of Port Said Hospitals
Port Said, Port Said Governorate, Egypt, 42515
Actively Recruiting
Research Team
M
Mohamed Mohamed Morgan, Bachelor of Physical Therapy
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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