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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age35-65
SponsorLudwig Boltzmann Institute for Cardiovascular Research

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Personal training

    Behavioral

    Personal training (strength and endurance, Yoga), nutrition and stress relief advices

  • App-based physical intervention

    Behavioral

    FEM-HEART specific App for life-style modifications including physical exercise, relaxation and nutrition

Treatment groups

605 Participants
are divided into 2 treatment groups
Group A: perimenopausal women with CVD riskActive comparator 2 interventions
Group B: postmenopausal women with CVD riskActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Changes in HRV prior to post intervention

Time frame
1 year intervention, 2 years follow-up

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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