Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06813677

Innsbruck Health Promotion Program

Led by VASCage GmbH · Updated on 2025-11-19

1000

Participants Needed

1

Research Sites

99 weeks

Total Duration

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Sponsors

V

VASCage GmbH

Lead Sponsor

O

Oroboros Instruments

Collaborating Sponsor

AI-Summary

What this Trial Is About

The primary goal of this single-centre. single-arm, unblinded, pre-post interventional study is to evaluate whether a one-time health assessment and intervention affects the overall vascular health evaluated through the Life's Essential 8 overall vascular health score. Secondary goals of this study are, among others: * to describe incidence and prevalence of vascular risk-factors and behaviours * to explore prevalence and associations of health and disease in the general population with special focus on cardiovascular risk, cardiovascular diseases, markers of vascular health, signs and (prodromal) symptoms of neurodegeneration as well as psychosocial factors * to explore the prevalence of hearing disorders in the general population * to collect voice and speech samples to identify novel biomarkers that correlate to vascular health and/or hearing status

CONDITIONS

Official Title

Innsbruck Health Promotion Program

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent of subject
  • Main area of residence in Innsbruck and Innsbruck-Land
Not Eligible

You will not qualify if you...

  • People who are suspended upon a court order or other legal processes, accommodated according to the Hospitalization Act, or have a custodian appointed or in process
  • Persons with impaired power of judgement
  • Persons who are currently engaged in military or community service

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Medical University Innsbruck - Department of Neurology

Innsbruck, Austria

Actively Recruiting

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Research Team

M

Muriel Harloff, MSc

CONTACT

P

Petr Simurda, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SCREENING

Number of Arms

1

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