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临床试验/NCT07577973
NCT07577973尚未招募不适用

The Effect of Self-Acupressure on Blood Pressure, Stress, and Well-Being Levels in Individuals With Hypertension: A Three-Arm Randomized Controlled Trial

Abant Izzet Baysal University1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2026年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
72
试验地点
1
主要终点
change in blood pressure

研究概览

简要总结

This randomized controlled trial examines the effects of nurse-led self-acupressure at HT7, LI4, PC6, and EX3 points on blood pressure, stress, and well-being in adults with primary hypertension. Participants are randomized to real acupressure, sham acupressure, or usual care groups for 2 weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18-65 years
  • Diagnosed with primary hypertension (Stage 1 or 2)
  • Systolic blood pressure 130-179 mmHg or diastolic 80-109 mmHg
  • Taking antihypertensive medication
  • Able to understand and communicate in Turkish
  • Willing to provide written informed consent

排除标准

  • Secondary hypertension
  • Pregnancy or lactation
  • Severe cardiovascular disease (heart failure, myocardial infarction within 6 months)
  • Stroke history within 6 months
  • Skin lesions or infection at acupressure sites (HT7, LI4, PC6, EX3)
  • Peripheral neuropathy affecting sensation
  • Current use of anticoagulant therapy
  • Participation in another clinical trial within 30 days

研究组 & 干预措施

Real Acupressure Group

Experimental

participants receive acupressure on bilateral HT7,LI4,PC6 EX3 points. pressure applied for 15 seconds per point, 3 days per week, for 2 weeks

干预措施: Real Acupressure (Behavioral)

sham/placebo

Sham Comparator

Participants receive sham acupressure on non-acupoints located 1-1.5 cm away from HT7, LI4 , PC6, and EX3 points. Pressure applied for 15 seconds per site, 3 days per week, for 2 weeks to maintain participant blinding

干预措施: sham acupressure (Behavioral)

control

Active Comparator

Participants receive usual care for hypertension including prescribed antihypertensive medications and routine clinical nursing follow-up for 2 weeks. No acupressure intervention applied.

干预措施: Usual Care (Other)

结局指标

主要结局

change in blood pressure

时间窗: baseline and week 2

change from baseline in systolic and diastolic blood pressure measured using an automated office blood pressure monitor at 2 weeks

次要结局

  • change in perceived stress(baseline, week 2)
  • change in mental well-being(baseline, week 2)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Saadet Can Çiçek

Asst. Prof.Saadet Can Cicek,Phd

Abant Izzet Baysal University

研究点 (1)

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