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NCT07318844Completed

Stroke Volume at Rest and During Exercise in Healthy Volunteers

Source: ClinicalTrials.gov · Last updated 6 Jan 2026

Brief summary (registry, in English)

Background Changes in cardiac output, driven by increased heart rate and stroke volume, are crucial for oxygen delivery during acute exercise and influence maximal oxygen uptake (VO₂max). Thoracic electrical bioimpedance provides a non-invasive alternative to traditional invasive methods by estimating stroke volume through impedance changes during ventricular filling and emptying. However, its test-retest reliability remains uncertain, requiring further investigation for use in acute and long-term training assessments. Methods Inclusion: 12 healthy individuals (six males, six females) Exclusion: Known ischaemic heart disease, known heart failure, symptoms of disease within 2 weeks prior to the study, known malignant disease, claudication, pregnancy, unstable cardiac arrhythmic disease, renal or liver dysfunction, known chronic lung disease Design: Test-retest study of thoracic electrical bioimpedance-based stroke volume Intervention: Acute exercise bout on a bicycle ergometer Statistical design: Rest-to-exercise changes, as well as between-day smallest real difference, coefficient of variation and intraclass correlation coefficient Sample size: Since this is a pilot study, the sample size is set at 12 in accordance with current recommendations. Perspective The results are relevant for designing future studies in which stroke volume is measured and compared in response to various interventions at rest and during exercise.

Status (registry)
Completed
Study type
Interventional
Enrollment
12 (actual)
First submitted
31 Aug 2025
Start date
1 Sept 2025
Primary completion date
1 Dec 2025
Lead sponsor
Copenhagen University Hospital, Rigshospitalet
Diseases
Stroke
NCT number
NCT07318844

What you commit to

  • Study type: Interventional
  • Participants enrolled: 12
  • From 1 Sept 2025 to the primary completion date, 1 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Symptoms of disease within 2 weeks prior to the study

Other illness

  • Known chronic lung disease
  • Known ischaemic heart disease
  • Known heart failure
  • Known malignant disease
  • Unstable cardiac arrhythmic disease

Other

  • Claudication
  • Pregnancy
  • Renal or liver dysfunction

Who the study is looking for

  • Men and women
  • 18-70 years

Age in the registry: 18 years to 70 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Trygfondens Center for Aktiv Sundhed
Coordinator of this site? Confirm its status
CopenhagenDenmarkUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.