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Patients´ Experiences of Calorimetry Measurements

18 septembre 2026 mis à jour par: Josefin Dimander, Uppsala University Hospital

A severe burn injury affects not only the skin but also how the body uses energy. Many patients have increased energy needs during recovery, and healthcare professionals use a method called indirect calorimetry to measure the body's energy expenditure and help provide appropriate nutritional treatment.

During the measurement, the patient rests comfortably while wearing a transparent canopy over the head for approximately 10 to 30 minutes. The equipment measures oxygen consumption and carbon dioxide production to estimate the body's energy needs.

Although indirect calorimetry is commonly used in burn care, little is known about how patients experience the procedure. The aim of this study is to explore patients' experiences of undergoing indirect calorimetry after a burn injury.

Participants will be interviewed about their experiences of the measurement. By analyzing these interviews, we hope to gain a better understanding of patients' perspectives and identify ways to improve information, preparation, comfort, and overall care related to the procedure. Ultimately, this may help make the assessment more comfortable for patients and support high-quality individualized nutritional treatment.

Aperçu de l'étude

Statut

Pas encore de recrutement

Description détaillée

Severe burn injury affects the entire body, not only the skin. Profound alterations occur in metabolism, endocrine function, and immune responses, resulting in a hypermetabolic state. This condition is characterized by an increased energy expenditure that may persist for months or even years following injury. Adequate nutritional support is essential to promote wound healing, reduce the risk of infection, and preserve lean body mass. Both underfeeding and overfeeding may adversely affect recovery and clinical outcomes.

To enable safe and individualized nutritional management, measurement of resting energy expenditure (REE) using indirect calorimetry is recommended. During the assessment, the awake patient wears a transparent plastic canopy placed over the head. Oxygen consumption and carbon dioxide production are measured over a period of 10 to 30 minutes to estimate energy requirements. Accurate measurements require the patient to remain still, relaxed, and awake, while refraining from speaking, as physical activity, psychological stress, and other disturbances may influence the results.

Although indirect calorimetry is routinely used in burn care, relatively little is known about how patients experience the measurement procedure itself. Factors such as the hospital environment, pain, anxiety, restricted mobility, and the measurement may influence the patient's experience; however, these aspects have received limited scientific attention. Understanding the patient perspective is important, as discomfort or stress may negatively affect both the patient experience and the quality of the measurement.

The aim of this study is therefore to explore how individuals receiving care for burn injuries experience the assessment of resting energy expenditure by indirect calorimetry.

Data will be collected through semi-structured interviews. Eligible participants will be approached during their burn care admission and provided with both oral and written study information. Written informed consent will be obtained prior to participation. Consent forms and interview data will be stored securely and will be accessible only to the research team.

Interviews will be conducted within two weeks of the indirect calorimetry assessment, either in person at the burn unit or remotely via telephone or video call following hospital discharge. All interviews will be audio-recorded and transcribed verbatim. The interview guide focuses on participants' experiences before, during, and after the indirect calorimetry measurement.

Data will be analyzed using inductive qualitative content analysis. Interview transcripts will be read repeatedly to achieve immersion in the data and identify meaning units, which will be condensed, coded, and grouped into subcategories, categories, and overarching themes. Two researchers will independently code the interviews and discuss interpretations until consensus is reached. The analysis will involve an iterative process of moving between the original text, codes, categories, and emerging themes to develop a comprehensive understanding of participants' experiences. Findings will be reported with illustrative quotations to enhance transparency and trustworthiness.

Through qualitative content analysis of interview data, the study seeks to provide an in-depth understanding of patients' experiences, perceptions, and needs associated with indirect calorimetry. Increased knowledge in this area may contribute to improvements in clinical procedures, patient communication, and preparation before and during the assessment. Ultimately, the goal is to make the measurement process as safe, comfortable, and patient-centered as possible, thereby enhancing both the patient experience and the quality of the measurements used to guide individualised nutritional therapy.

Type d'étude

Observationnel

Inscription (Estimé)

20

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

Sauvegarde des contacts de l'étude

  • Nom: Anna Stenson Zerpe, PhD, PhD
  • Numéro de téléphone: +46(0)186119466
  • E-mail: anna.zerpe@uu.se

Lieux d'étude

      • Uppsala, Suède, 75185
        • Uppsala university hospital
        • Contact:
        • Contact:
          • Anna Stenson Zerpe, PhD
          • Numéro de téléphone: +46(0)186119466
          • E-mail: anna.zerpe@uu.se
        • Chercheur principal:
          • Josefin Dimander, PhD
        • Chercheur principal:
          • Anna Stenson Zerpe, PhD

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 et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

Patients post-burn admitted to the BurnCentre at Uppsala university hospital, 18 years or older, swedish/english speaking, with experience of at least one calorimetry measurement.

La description

Inclusion Criteria:

  • Patients post-burn admitted to the BurnCentre at Uppsala university hospital
  • 18 years or older
  • Swedish/english speaking
  • With experience of at least one calorimetry measurement during burn care post-trauma

Exclusion Criteria:

  • Not fulfilling inclusion criteria

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

  • Modèles d'observation: OTHER
  • Perspectives temporelles: OTHER

Cohortes et interventions

Groupe / Cohorte
Patients post-burn

Patients post-burn admitted to the BurnCentre at Uppsala university hospital, 18 years or older, swedish/english speaking, with experience of at least one calorimetry measurement.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Patients´ experiences
Délai: The interviews will be conducted within two weeks from the calorimetry measurment.

Patients´ experiences before, during and after calorimetry measurement is explored with a semi-structered interview guide. The interview will be conducted within two weeks from the measurment at the Burn Centre. The interviews will be recorded, transcribed and analysed with content analysis.

The interviews will be conducted within two weeks from the calorimetry measurment.

Collaborateurs et enquêteurs

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

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

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 septembre 2026

Achèvement primaire (Estimé)

1 juin 2028

Achèvement de l'étude (Estimé)

1 juin 2029

Dates d'inscription aux études

Première soumission

10 septembre 2026

Première soumission répondant aux critères de contrôle qualité

18 septembre 2026

Première publication (Réel)

24 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

24 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

18 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • FOU2026-00337

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

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 .

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