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Acute Effect of Aerobic Exercise on Cardiovascular Reactivity During a Mental Stress Test in Teachers

27 octobre 2026 mis à jour par: Lucieli Teresa Cambri, Federal University of Mato Grosso

Acute Effect of Moderate-intensity Aerobic Exercise on Cardiovascular Reactivity During a Mental Stress Test in Teachers

This study will investigate the acute effect of a single session of moderate-intensity aerobic exercise on blood pressure responses to mental stress in teachers. Participants will complete two experimental sessions: a control session without exercise and a 30-minute moderate-intensity aerobic exercise session. The intensity of the aerobic exercise session will be set at 50-60% of the heart rate reserve. The order of the experimental sessions will be randomized. We will assess blood pressure and heart rate at rest and during a mental stress test performed before and 30 minutes after each session. The two sessions will be separated by 48-72 hours.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Description détaillée

This study will investigate the acute effects of a moderate-intensity aerobic exercise session on blood pressure responses to mental stress in teachers. Participants will complete two experimental sessions: a control session without exercise and a 30-minute moderate-intensity aerobic exercise session. The intensity of the aerobic exercise session will be set at 50-60% of the heart rate reserve. The order of the experimental sessions will be randomized. We will assess blood pressure and heart rate at rest and during a mental stress test performed before and 30 minutes after each session. The two sessions will be separated by 48-72 hours.

The mental stress test will consist of a computerized Stroop Color Test involving the colors green, red, blue, and yellow. Participants will be instructed to identify the color of the word rather than read the word itself. For example, if the word "green" is displayed in red, the correct response is "red." Each word will be displayed for one second. An auditory stimulus consisting of words that differ from both the written word and the displayed color will also be presented. The total duration of the mental stress test will be 4 minutes (Probst et al., 1997; Cavalcante, 2023).

Systolic blood pressure (SBP), diastolic blood pressure (DBP), and HR will be assessed at baseline and during the mental stress test (at 2 and 4 minutes) performed before and 30 minutes after each session.

Mental stress reactivity (Δ) will be calculated at 2 and 4 minutes as the value measured at each time point minus the corresponding pre-test baseline value (Δ2 = value at 2 minutes - baseline value; Δ4 = value at 4 minutes - baseline value). Peak Δ will be defined as the highest response observed at either 2 or 4 minutes (the maximum of Δ2 and Δ4). The change in blood pressure reactivity from before to 30 minutes after each experimental session will be compared between the moderate-intensity aerobic exercise and control conditions.

Type d'étude

Interventionnel

Inscription (Estimé)

25

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Mato Grosso
      • Cuiabá, Mato Grosso, Brésil, 78.060-581
        • Federal University of Mato Grosso

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 65 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

Participants must meet all of the following criteria:

  • Age between 18 and 65 years;
  • Body mass index (BMI) between 18.5 and 39.9 kg/m²;
  • Currently employed as a teacher;
  • At least 2 years of experience as a teacher;
  • Able to perform the proposed physical exercise interventions.

Exclusion Criteria:

  • Have a psychiatric disorder that could interfere with participation in the study;
  • Have a diagnosed cardiac arrhythmia;
  • Have musculoskeletal or osteoarticular conditions that prevent or contraindicate physical exercise;
  • Are pregnant or breastfeeding;
  • Are on leave of absence or vacation during the study period.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation croisée
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur factice: Contrôle

Participants will undergo a control session without physical exercise. Blood pressure and heart rate will be assessed at rest and during the Stroop Color Test, performed before and 30 minutes after the control session.

Expérimental: Exercice aérobique d'intensité modérée

Participants will perform a 30-minute moderate-intensity aerobic exercise session at 50-60% of the heart rate reserve. Blood pressure and heart rate will be assessed at rest and during the Stroop Color Test, performed before and 30 minutes after the exercise session.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Systolic blood pressure reactivity to mental stress
Délai: During the mental stress test (0, 2 and 4 minutes), before and 30 minutes after each experimental session.

Systolic blood pressure will be measured at rest and during the Stroop Color Test before and 30 minutes after each experimental session. Systolic blood pressure reactivity to mental stress will be calculated as the change (Δ) in systolic blood pressure between the resting measurement and the measurement obtained during the Stroop Color Test.

The change in systolic blood pressure reactivity from before to 30 minutes after each experimental session will be compared between the session of moderate-intensity aerobic exercise and control conditions.

During the mental stress test (0, 2 and 4 minutes), before and 30 minutes after each experimental session.
Post-exercise hypotension
Délai: At rest before and 30 minutes after each experimental session.

Post-exercise hypotension will be assessed by comparing systolic and diastolic blood pressure measured 30 minutes after each experimental session with the corresponding pre-exercise resting measurements.

At rest before and 30 minutes after each experimental session.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Diastolic blood pressure reactivity to mental stress
Délai: During the mental stress test (0, 2 and 4 minutes), before and 30 minutes after each experimental session.

Diastolic blood pressure reactivity to mental stress will be calculated as the change (Δ) in diastolic blood pressure between the resting measurement and the measurement obtained during the Stroop Color Test. The change in diastolic blood pressure reactivity from before to 30 minutes after each experimental session will be compared between the session of moderate-intensity aerobic exercise and control conditions.

During the mental stress test (0, 2 and 4 minutes), before and 30 minutes after each experimental session.
Heart rate reactivity to mental stress
Délai: During the mental stress test (0, 2 and 4 minutes), before and 30 minutes after each experimental session.

Heart rate reactivity to mental stress will be calculated as the change (Δ) in heart rate between the resting measurement and the measurement obtained during the Stroop Color Test. The change in heart rate reactivity from before to 30 minutes after each experimental session will be comparedthe session of moderate-intensity aerobic exercise and control conditions.

During the mental stress test (0, 2 and 4 minutes), before and 30 minutes after each experimental session.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 décembre 2026

Achèvement primaire (Estimé)

1 décembre 2028

Achèvement de l'étude (Estimé)

1 décembre 2028

Dates d'inscription aux études

Première soumission

27 octobre 2026

Première soumission répondant aux critères de contrôle qualité

27 octobre 2026

Première publication (Réel)

3 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

3 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

27 octobre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

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Informations sur les médicaments et les dispositifs, documents d'étude

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