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Trial · NCT06533982

Registered outcomes27

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimarySystolic and diastolic blood pressure (ambulatory blood pressure measurement)After sessions (24 hours)Post-exercise hypotension, using the Mobil-O-Graph (mmHg).
PrimarySystolic and diastolic blood pressure (resting)Before and after sessions (15 minutes)Automated oscillometric tensiometer (mmHg).
SecondaryConcentration of cerebral oxygenationBefore, during, and after sessions (1 hour)Near-infrared spectroscopy is used to measure concentrations of oxygenated and desoxygenated hemoglobin (µmol/L).
SecondaryWorking memoryBefore and after sessions (10 minutes)2-back task (scored from 0 to 28, higher scores indicate better working memory).
SecondaryEpisodic memoryBefore and after sessions (15 minutes)Memory scale III (MEM-III), a story recall task taken from the test battery in the Wechsler-Memory Scale-Revised (scored from 0 to 25, higher scores indicate better episodic memory).
SecondaryExecutive functionBefore and after sessions (15 minutes)Stroop task, used to assess inhibitory control (scored as a ratio, negative score indicates worse inhibitory control vs. positive score indicates better inhibitory control).
SecondaryPerception of exertionAfter sessions (1 minute)Modified Borg scale (scored 0 to 10, higher score indicates lower exercise tolerance).
SecondaryEndothelial function (brachial artery dilation capacity)Baseline (30 minutes)At rest, the flow-mediated dilatation technique is used with high-resolution Doppler ultrasound (CX-50 Philipps).
SecondaryBaroreflex sensitivityBaseline (1 hour)At rest, baroreflex sensitivity is measured using the Finapres.
SecondaryAortic systolic and diastolic blood pressureBaseline (15 minutes)At rest, using the SphygmoCor device, which measures central blood pressure (mmHg).
SecondaryArterial stiffness (pulse wave velocity)Baseline (15 minutes)At rest, using the SphygmoCor device, which calculates carotid-femoral pulse wave velocity (m/s).
SecondaryPhysical fitnessBaseline (30 minutes)Maximal cardiopulmonary effort test (VO2max).
SecondaryBlood lipid concentrationsBaseline (5 minutes)Total cholesterol, high-density lipoprotein (HDL), low-density lipoprotein (LDL), and triglycerides (g/L).
SecondaryBlood hormone concentrationsBaseline (5 minutes)Progesterone, 17-beta-estradiol, and follicle-stimulating hormone (ng/L).
SecondaryBody weightBaseline (1 minute)Total body weight, fat mass, fat-free mass and visceral-fat mass in kilograms using the Tanita impedance scale.
SecondaryBody compositionBaseline (1 minute)Percentage of body fat and fat-free mass using the Tanita impedance scale.
SecondaryHeightBaseline (1 minute)Height in meters measured with a height gauge.
SecondaryBody mass indexBaseline (1 minute)Calculated from total body weight and height (kg/m²).
SecondaryCognitive assessmentBaseline (15 minutes)Montreal Cognitive Assessment (MoCA) test (scored from 0 to 30, with higher scores indicating better cognitive function).
SecondaryMenopausal rating scaleBaseline (15 minutes)Composed of 11 items rating the severity of menopausal symptoms from 0 (no symptoms) to 4 (very severe).

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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