跳至主要内容
临床试验/NCT07703124
NCT07703124尚未招募不适用

Female-Specific Modifiers for Healthy Early Action in Cardiovascular Risk Trajectories

Ludwig Boltzmann Institute for Cardiovascular Research0 个研究点目标入组 605 人开始时间: 2027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
发起方
入组人数
605
主要终点
Changes in HRV prior to post intervention

研究概览

简要总结

Cardiovascular disease is the leading cause of death in women, yet risk is systematically underestimated and preventive interventions are often initiated too late. Women are disproportionately affected by obesity, diabetes, and smoking, but they also derive greater cardioprotective benefit from physical activity, reaching near-maximal protection at approximately half the exercise dose required in men. FEM-HEART targets a critical pre-clinical window by testing whether a personalized app-based intervention and a supervised face-to-face lifestyle program, both integrating tailored exercise, nutrition, and stress reduction, can improve early cardiovascular risk profiles in high-risk women during the peri- and postmenopausal transition.

In this prospective randomized controlled trial embedded in routine preventive care at SVS Gesundheitszentrum, 605 women will be randomized to a digital arm, a supervised intervention arm, or an untreated control group. The study will evaluate whether digital and supervised delivery formats differ in their ability to modify early cardiovascular trajectories before overt disease onset.

By targeting this modifiable pre-clinical phase, FEM-HEART shifts cardiovascular prevention from reactive care to proactive, sex-specific risk reduction and lays the foundation for scalable, woman-centered prevention strategies.

研究设计

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

入排标准

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

入选标准

  • women aged >35 years in the perimenopausal transition
  • women within 5 years after menopause and and younger than 65 years
  • women with two of the following: (i) established cardiovascular risk factors, such as hypertension, dyslipidemia, overweight, or smoking; (ii) female-specific and hormone-related factors, such as pregnancy-associated complications or early menarche; and (iii) elevated psychosocial stress, assessed by validated questionnaires and physiological proxies.

排除标准

  • high levels of physical activity
  • hormone replacement therapy
  • major comorbidities such as diabetes, moderate-to-severe kidney or liver disease, malignant tumors, musculoskeletal or neurological conditions limiting mobility, congenital heart defects, prior cardiac events, or a history of thrombosis.

研究组 & 干预措施

postmenopausal women with CVD risk

Active Comparator

干预措施: Personal training (Behavioral)

postmenopausal women with CVD risk

Active Comparator

干预措施: App-based physical intervention (Behavioral)

perimenopausal women with CVD risk

Active Comparator

干预措施: Personal training (Behavioral)

perimenopausal women with CVD risk

Active Comparator

干预措施: App-based physical intervention (Behavioral)

结局指标

主要结局

Changes in HRV prior to post intervention

时间窗: 1 year intervention, 2 years follow-up

次要结局

未报告次要终点

研究者

发起方
Ludwig Boltzmann Institute for Cardiovascular Research
申办方类型
Other
责任方
Sponsor

相似试验