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Patients´ Experiences of Calorimetry Measurements

18 september 2026 uppdaterad av: 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.

Studieöversikt

Status

Har inte rekryterat ännu

Detaljerad beskrivning

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.

Studietyp

Observationell

Inskrivning (Beräknad)

20

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studera Kontakt Backup

  • Namn: Anna Stenson Zerpe, PhD, PhD
  • Telefonnummer: +46(0)186119466
  • E-post: anna.zerpe@uu.se

Studieorter

      • Uppsala, Sverige, 75185
        • Uppsala university hospital
        • Kontakt:
        • Kontakt:
          • Anna Stenson Zerpe, PhD
          • Telefonnummer: +46(0)186119466
          • E-post: anna.zerpe@uu.se
        • Huvudutredare:
          • Josefin Dimander, PhD
        • Huvudutredare:
          • Anna Stenson Zerpe, PhD

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Testmetod

Icke-sannolikhetsprov

Studera befolkning

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.

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Observationsmodeller: OTHER
  • Tidsperspektiv: OTHER

Kohorter och interventioner

Grupp / Kohort
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.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Patients´ experiences
Tidsram: 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.

Samarbetspartners och utredare

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Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Allmänna publikationer

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 september 2026

Primärt slutförande (Beräknad)

1 juni 2028

Avslutad studie (Beräknad)

1 juni 2029

Studieregistreringsdatum

Först inskickad

10 september 2026

Först inskickad som uppfyllde QC-kriterierna

18 september 2026

Första postat (Faktisk)

24 september 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

24 september 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

18 september 2026

Senast verifierad

1 september 2026

Mer information

Termer relaterade till denna studie

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • FOU2026-00337

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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