Acupuncture Therapy and Hypertension
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: electroacupuncture.
- Who it may be relevant to
- Registry conditions: Mild to Moderate Hypertension. Basic parameters: 45 years — 75 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Neuroimmune Mechanisms Underlying Electroacupuncture Effect on Vascular Function
Overview
Acupuncture therapy will be provided to reduce blood pressure in hypertensive patients. The mild to moderate hypertensive patients will be either on or off hypertensive medications. The course last for 8 weeks and the frequency is once a week.
Detailed description
Improvement in BP control rates would lead to one of the largest impacts in improving life expectancy and the quality of life for over 100 million people in the United States and 1 billion people worldwide with immediate and measurable results. In the United States, 80% of patients with HTN are treated, but BP is controlled in only half of these individuals, with control worsening with increasing age. The reasons for inadequate treatment and BP control are complex, but one reason for this therapeutic misalignment may be an incomplete understanding of the mechanisms underlying the development and progression of HTN. The aging process leads to dysfunction of the ANS, resulting in neuroendocrine abnormalities and chronic low-grade inflammation.
The investigators have previously shown that electroacupuncture (EA) at four targeted acupoints, can decrease sympathetic activity \[sympathoinhibitory (SI)\], approaching levels close to those present prior to onset of HTN and may address this unmet need in HTN management. The investigators are now testing and have preliminary evidence that EA at two additional acupoints (SP6-7) increases parasympathetic activation, thereby decreasing circulating and tissue inflammatory biomarkers \[thus anti-inflammatory (AI)\] and when combined with SI-EA can improve measures of vascular health including endothelial function and arterial stiffness in preclinical model with overall greater reduction in BP. Together these combined six acupoints, when simultaneously activated by EA may restore optimal autonomic control of the immune system and target an important mechanistic pathway not addressed by BP-lowering pharmacotherapy alone. To date, 39 participants have been enrolled in the study.
Interventions
- Other electroacupuncture
acupuncture needling and stimulation are applied for 30 min
Primary outcome measures
- Changes in sympathetic and parasympathetic nervous systems [Time frame: through study completion, an average of 4.5 years]
Secondary outcome measures (1)
- Change in biomarkers like cytokines [Time frame: through study completion, an average of 4.5 years]
Eligibility criteria
Inclusion criteria
- Subjects from 45 to 75 years of age
- Clinically diagnosed with mild to moderate hypertension and ON or OFF medication (Office SBP > 140 mmHg and < 160 mmHg Or ABPM average SBP > 130 mmHg and < 145 mmHg), and
- No significant ECG change reflecting ischemia (i.e. ST elevation or depression) at rest will be recruited to participate in this study.
Exclusion criteria
- Subjects will be excluded if pregnant or nursing.
- Subjects will be excluded if they have coronary disease (by history or on ECG screening), conduction abnormalities on ECG consistent with left bundle branch block, cardiac arrhythmias associated with low blood pressure (<90 mmHg), peripheral vascular disease, orthopedic disease, diabetic neuropathy or severe hypertension (BP >170 mmHg systolic or >110 mmHg diastolic), or any other physical or psychological illness.
- Those with known sensitivity to any topical preparations or strong reactions to medical dressings and skin tapes also will be excluded.
- Inability our or unwillingness of individual to give written informed consent.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Factorial
- Masking
- Triple blind
- Primary purpose
- Basic science
Study locations
United States · 2 centers
- Susan Samueli Integrative Health Institute — Irvine
- University of California, Irvine, Health Sciences Medical Center — Orange
Identifiers
NCT: NCT05530512 · 19992222 · R01AT011306