- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02507869
A Trial of an Affect-Guided Physical Activity Prescription
23 juillet 2015 mis à jour par: Austin Baldwin, Southern Methodist University
A Pilot Randomized Controlled Trial of an Affect-Guided Physical Activity
Despite awareness of the benefits of engaging in regular physical activity, at least 50% of adults in the US do not meet recommended guidelines for physical activity.
One potential explanation for this lack of regular physical activity is that people often experience exercise as affectively unpleasant.
Evidence suggests that the more positively people experience exercise (i.e., the better they feel while exercising), the more likely they are to engage in regular physical activity.
This may be especially true for people in poor cardiorespiratory condition.
In this randomized trial, investigators compared the effects of an affect-guided exercise prescription (intervention) to a heart rate-guided exercise prescription (control) on change in physical activity minutes among previously underactive adults.
Investigators also tested whether the effect of the intervention was moderated by differences in cardiorespiratory fitness.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Description détaillée
Regular physical activity has many benefits for overall health and well-being, and current public health guidelines recommend at least 150 minutes per week of moderate-to-vigorous intensity activity to attain these benefits.
Despite the many benefits of regular activity, the majority of adults in the US fail to meet recommendations for regular physical activity.
One potential explanation for suboptimal levels of physical activity is that exercise is often experienced as affectively unpleasant.
Recent work has demonstrated that the more positive people feel during exercise, the more likely they are to engage in regular physical activity.
Affective response to exercise is modulated by the intensity of the activity: at a vigorous intensity, affective response is almost uniformly negative and unpleasant, whereas at a moderate intensity, there is more inter-individual variability in affective response.
Whether the intensity of the exercise is self-selected or imposed also influences the affective response to exercise, with self-selected intensities being experienced as more pleasant.
Current recommendations for engaging in physical activity focus on the type of training intensities most likely to result in a negative affective response.
The purpose of this pilot trial was to test the effects of an exercise prescription focused on the maintenance of positive affect during exercise.
Investigators randomized participants to one of two exercise prescription conditions: (1) an affect-guided prescription focused on maintaining a positive affective response (intervention), and (2) a heart rate-guided prescription focused on maintaining a moderate intensity (control).
Investigators tested the effects of these two exercise prescriptions on changes in subsequent physical activity after one week and one month among a sample of underactive adults.
Investigators also tested whether the effect of the intervention was moderated by differences in cardiorespiratory fitness.
Type d'étude
Interventionnel
Inscription (Réel)
67
Phase
- N'est pas applicable
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:
- Physically underactive individuals (< 60 minutes of physical activity/week).
Exclusion Criteria:
- Presence of cardiovascular disease, pulmonary disease, or hypertension.
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 parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Affect-Guided Prescription
Intervention: Participants in the affect-guided condition are instructed to exercise while monitoring how they feel, and to adjust the intensity of their exercise to maintain a pleasant affective response.
|
Participants adjust the intensity of their exercise to maintain a pleasant affective response.
|
|
Comparateur actif: Heart Rate-Guided Prescription
Intervention: Participants in the heart rate-guided condition are instructed to exercise while monitoring their heart rate, and to adjust the intensity of the exercise to maintain a heart rate in the moderate range (64-76% of their HRmax).
|
Participants adjust the intensity of the exercise to maintain a heart rate in the moderate range (64-76% of their HRmax).
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Change in physical activity minutes measured by the 7-day PAR
Délai: One week
|
One week
|
|
Change in physical activity minutes measured by the 7-day PAR
Délai: One month
|
One month
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Austin Baldwin, Ph.D., Southern Methodist University
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
- Ekkekakis P, Lind E. Exercise does not feel the same when you are overweight: the impact of self-selected and imposed intensity on affect and exertion. Int J Obes (Lond). 2006 Apr;30(4):652-60. doi: 10.1038/sj.ijo.0803052.
- Ekkekakis P, Parfitt G, Petruzzello SJ. The pleasure and displeasure people feel when they exercise at different intensities: decennial update and progress towards a tripartite rationale for exercise intensity prescription. Sports Med. 2011 Aug 1;41(8):641-71. doi: 10.2165/11590680-000000000-00000.
- Williams DM, Dunsiger S, Miranda R Jr, Gwaltney CJ, Emerson JA, Monti PM, Parisi AF. Recommending self-paced exercise among overweight and obese adults: a randomized pilot study. Ann Behav Med. 2015 Apr;49(2):280-5. doi: 10.1007/s12160-014-9642-7.
- Ekkekakis P, Lind E, Vazou S. Affective responses to increasing levels of exercise intensity in normal-weight, overweight, and obese middle-aged women. Obesity (Silver Spring). 2010 Jan;18(1):79-85. doi: 10.1038/oby.2009.204. Epub 2009 Jun 25.
- Parfitt G, Alrumh A, Rowlands AV. Affect-regulated exercise intensity: does training at an intensity that feels 'good' improve physical health? J Sci Med Sport. 2012 Nov;15(6):548-53. doi: 10.1016/j.jsams.2012.01.005. Epub 2012 May 31.
- Williams DM, Dunsiger S, Jennings EG, Marcus BH. Does affective valence during and immediately following a 10-min walk predict concurrent and future physical activity? Ann Behav Med. 2012 Aug;44(1):43-51. doi: 10.1007/s12160-012-9362-9.
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
1 avril 2013
Achèvement primaire (Réel)
1 avril 2014
Achèvement de l'étude (Réel)
1 avril 2014
Dates d'inscription aux études
Première soumission
22 juillet 2015
Première soumission répondant aux critères de contrôle qualité
23 juillet 2015
Première publication (Estimation)
24 juillet 2015
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
24 juillet 2015
Dernière mise à jour soumise répondant aux critères de contrôle qualité
23 juillet 2015
Dernière vérification
1 juillet 2015
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- 2012-098-SMIJ
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 .