Effects of Cold-Water and Cold-Air Exercise on Appetite, Energy Intake, and Food Preference
2 juillet 2026 mis à jour par: Marie Hutson, Coventry University
Effects of Exercising in Cold-Water and Cold-Ambient Air Versus a Thermoneutral Equivalent on Appetite, Energy Intake, and Food Preference: A Crossover Study in Healthy Males
This study investigated whether exercising in cold environments affects appetite, energy intake, and food preference compared with exercising in thermoneutral conditions.
Eleven healthy males completed five laboratory trials as part of a crossover study: a control trial and four exercise trials performed in cold-water (16°C), thermoneutral water (35°C), cold-ambient air (6°C), and thermoneutral ambient air (26°C).
Appetite responses were assessed throughout each trial, and participants were provided with an ad libitum meal after exercise to measure energy intake.
Food preference was assessed using the Leeds Food Preference Questionnaire.
The study aimed to determine whether environmental temperature and exercise medium influence acute post-exercise eating behaviour.
Aperçu de l'étude
Statut
Complété
Les conditions
Description détaillée
Exercise performed in cold environments may influence thermoregulatory responses and subsequent eating behaviour differently compared with exercise performed under thermoneutral conditions. Previous research suggests that cold exposure may increase post-exercise energy intake; however, the influence of environmental temperature and exercise medium (water versus air) on appetite regulation and food-related behaviour remains unclear.
This study used a randomised repeated-measures crossover design to investigate the effects of cold and thermoneutral exercise conditions on appetite, energy intake, and food preference in healthy males.
Eleven healthy males completed five laboratory trials: a no-exercise control condition and four experimental exercise conditions consisting of 30 minutes of arm-leg rowing exercise performed in cold-water (16°C), thermoneutral water (35°C), cold-ambient air (6°C), and thermoneutral ambient air (26°C). Trials were separated by a minimum seven-day washout period.
Appetite responses were assessed using visual analogue scales throughout each trial. Following exercise, participants consumed an ad libitum meal to assess acute post-exercise energy intake. Food preference responses, including food appeal and preference measures, were assessed using the Leeds Food Preference Questionnaire.
The primary objective was to determine whether environmental temperature and exercise medium influence post-exercise energy intake. Secondary objectives were to examine effects on subjective appetite and food preference measures.
This study provides insight into how exercising in different thermal environments may influence immediate eating behaviour following exercise.
Type d'étude
Interventionnel
Inscription (Réel)
11
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.
Lieux d'étude
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Coventry, Royaume-Uni, CV1 5FB
- Centre for Physical Activity, Sport and Exercise Sciences, Research Laboratory, Coventry University
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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
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Oui
La description
Inclusion Criteria:
- Healthy males aged 18-65 years
- Living in the UK
- Recreationally active and meeting current physical activity guidelines
- Body mass stable (<2 kg change) during the 3 months prior to the study
- Able to complete moderate-intensity arm-leg rowing exercise
- Able to tolerate the cold-water familiarisation/tolerance test
- Low cognitive restraint score on the Three-Factor Eating Questionnaire Revised
- 18-item (TFEQ-R18)
- Able to consume the standardised breakfast and ad libitum pasta meal provided during the study
- Able to provide written informed consent
- Willing to complete study questionnaires and experimental assessments
- Willing to undergo core temperature measurement via self-inserted rectal thermistor and body composition assessment
Exclusion Criteria:
- Diagnosed cardiovascular, pulmonary, metabolic, or renal disease, or symptoms suggestive of these conditions
- Any contraindication to moderate-intensity exercise
- Conditions increasing risk during cold exposure, including history of cold-induced asthma, Raynaud's phenomenon, cold urticaria, or other non-freezing cold injuries
- Cold-habituated individuals (e.g., regular cold-water swimmers)
- Current medication known to alter body weight or metabolism
- Smoking, drug misuse, or alcohol abuse
- Current musculoskeletal injury or condition that could be worsened by exercise
- History of eating disorders or restrained eating behaviour
- Shift work or sleep deprivation affecting study participation
- Unable to fast before experimental sessions
- Unable to tolerate the cold-water familiarisation/tolerance procedure
- Unable to consume the foods provided as part of the standardised breakfast or ad libitum meal due to dietary restrictions or allergies
- Unable to commit to study requirements
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: Science basique
- Répartition: Randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
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Comparateur actif: Control Condition
Resting control condition with no exercise performed.
Participants completed the same standardised laboratory procedures and outcome assessments under resting conditions.
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Resting control condition with no exercise exposure.
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Expérimental: Cold-Water Exercise
Participants completed 30 minutes of arm-leg rowing exercise performed in cold water at 16°C.
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Arm-leg rowing exercise performed in 16°C water.
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Expérimental: Thermoneutral Water Exercise
Participants completed 30 minutes of arm-leg rowing exercise performed in thermoneutral water at 35°C.
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Arm-leg rowing exercise performed in 35°C water.
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Expérimental: Cold-Ambient Air Exercise
Participants completed 30 minutes of arm-leg rowing exercise performed in cold ambient air at 6°C.
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Arm-leg rowing exercise performed in 6°C ambient air.
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Expérimental: Thermoneutral Ambient Air Exercise
Participants completed 30 minutes of arm-leg rowing exercise performed in thermoneutral ambient air at 26°C.
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Arm-leg rowing exercise performed in 26°C ambient air.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
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Post-exercise ad libitum energy intake
Délai: 30 minutes after completion of the 30-minute experimental/control condition.
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Energy intake consumed during an ad libitum homogeneous pasta meal provided after each 30-minute experimental/control condition.
The mass of food consumed was determined by subtracting the mass of food remaining (including leftovers on the plate and cutlery).
Absolute energy intake was calculated using the nutritional information provided by the food manufacturer.
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30 minutes after completion of the 30-minute experimental/control condition.
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Subjective appetite responses
Délai: Before and after breakfast, before the 30-minute experimental/control condition, during the 30-minute experimental/control condition, and before and after the ad libitum meal.
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Subjective appetite responses including hunger, fullness, satisfaction, and prospective food consumption assessed using a 100-mm Visual Analogue Scale (VAS) ranging from 0 mm (not at all) to 100 mm (extremely).
Higher scores indicate greater subjective appetite sensations.
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Before and after breakfast, before the 30-minute experimental/control condition, during the 30-minute experimental/control condition, and before and after the ad libitum meal.
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Food preference and food reward responses
Délai: 15 minutes after completion of each 30-minute experimental/control trial and 15-minutes before the ad libitum meal.
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Food preference and reward responses assessed using the Leeds Food Preference Questionnaire (LFPQ).
Outcomes include explicit liking, explicit wanting, implicit wanting, and fat and sweet appeal bias scores.
Higher scores indicate greater preference or reward response for the respective food category (fat or sweet).
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15 minutes after completion of each 30-minute experimental/control trial and 15-minutes before the ad libitum meal.
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
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Energy expenditure
Délai: During the 30-minute experimental/control condition.
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Energy expenditure during the exercise/control condition estimated from breath-by-breath oxygen consumption and carbon dioxide production using indirect calorimetry.
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During the 30-minute experimental/control condition.
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Skin temperature and mean body temperature responses
Délai: 5-minutes before and 5-minutes after the 30-minute experimental/control condition.
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Skin temperature was measured at four sites (chest, bicep, thigh, and calf) using skin temperature probes.
Mean skin temperature and mean body temperature were calculated to assess changes in peripheral and overall thermal status.
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5-minutes before and 5-minutes after the 30-minute experimental/control condition.
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Core body temperature
Délai: During the 30-minute experimental/control condition and during the 60-minute post-exposure recovery period.
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Changes in core body temperature measured continuously using a rectal thermistor during and after each experimental/control condition.
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During the 30-minute experimental/control condition and during the 60-minute post-exposure recovery period.
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Thermal sensation and shivering responses
Délai: During the 30-minute experimental/control condition at 10-minute intervals.
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Thermal sensation was assessed using the American Society of Heating, Refrigerating and Air-Conditioning Engineers (ASHRAE) 7-point Thermal Sensation Scale, ranging from -3 (cold) to +3 (hot), where 0 indicates thermal neutrality. Shivering responses were assessed using the Bedside Shivering Assessment Scale (BSAS) ranging from 0 (no shivering) to 3 (severe shivering), with higher scores indicating greater shivering severity. |
During the 30-minute experimental/control condition at 10-minute intervals.
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
Publications générales
- Grigg MJ, Thake CD, Allgrove JE, King JA, Thackray AE, Stensel DJ, Owen A, Broom DR. Influence of water-based exercise on energy intake, appetite, and appetite-related hormones in adults: A systematic review and meta-analysis. Appetite. 2023 Jan 1;180:106375. doi: 10.1016/j.appet.2022.106375. Epub 2022 Nov 12.
- Grigg MJ, Thake CD, Allgrove JE, Broom DR. Effects of cold-water immersion on energy expenditure, ad-libitum energy intake and appetite in healthy adults. Physiol Behav. 2025 Jul 1;296:114914. doi: 10.1016/j.physbeh.2025.114914. Epub 2025 Apr 10.
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 (Réel)
7 janvier 2025
Achèvement primaire (Réel)
2 juillet 2025
Achèvement de l'étude (Réel)
2 juillet 2025
Dates d'inscription aux études
Première soumission
26 juin 2026
Première soumission répondant aux critères de contrôle qualité
26 juin 2026
Première publication (Réel)
2 juillet 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
6 juillet 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
2 juillet 2026
Dernière vérification
1 juillet 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- P180097
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Description du régime IPD
Individual participant data will not be shared.
Study results will be reported in aggregate form through publications and presentations.
Data will be retained securely in accordance with Coventry University research governance and data protection requirements.
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .