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Completed

NCT Number: NCT07180238

Concept Elicitation and Patient Experience Mapping in SA-AKI

This is a concept elicitation study on patient's experiences of Sepsis-associated Acute Kidney Injury (SA-AKI)

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Key information

About this study

The purpose of this study is to elicit concepts of interests in patients who experienced SA-AKI. The study also aims to map experiences from patient and caregiver perspectives, including treatment pathways and barriers to SA-AKI treatment, the burden of SA-AKI and unmet needs, and the disease's humanistic, societal, and economic impacts. This study is a cross-sectional, non-interventional qualitative interview study of up to 30 people who have experienced SA-AKI from the US and Germany. Participants will be screened for eligibility, provide consent, and complete a virtual, hybrid 60-minute semi-structured concept elicitation (CE) and patient experience interview. Transcripts will be reviewed by analysts and analysed according to a qualitative analysis plan including a thematic analysis of the coded transcripts. This is a minimal risk study. All information will be kept confidential, and information will be stored on a secure network which is only accessible to the study team.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Potential participants who were diagnosed with SA-AKI (KDIGO stage I, II or III) must meet the following eligibility criteria:

  • ≥18 to ≤ 85 years of age
  • First diagnosis of SA-AKI at least 6 months prior to screening date, but no more than 10 years
  • Admitted due to sepsis and/or AKI to intensive care unit (ICU), intermediate care unit (IMCU), or high-dependency care unit, or developed sepsis and/or AKI during their inpatient hospital stay.
  • Resident of country of study (US or Germany)
  • Access to computer, tablet, or smartphone with internet connection
  • Willing to participate in an audio recorded interview

Participants will be required to present confirmation of diagnosis (COD) rather than relying on a self-reported diagnosis. Sepsis and AKI diagnoses will be confirmed through one of the following:

  • Copy of medical records (e.g., portable document format [PDF] file of electronic health record)
  • Physician confirmation of diagnosis of sepsis and AKI (post-sepsis)

Potential caregiver participants must meet the following criteria:

  • ≥18 to ≤ 85 years of age
  • Primary caregiver/care-partner for eligible participant who experienced SA-AKI
  • Resident of country of study (US or Germany)
  • Access to computer, tablet, or smartphone with internet connection
  • Willing to participate in an audio recorded interview

Exclusion criteria

Potential participants are not eligible if they meet any of the following criteria:

  • Less than age of majority in locality (Participant is not considered an adult in their country or region)
  • Not willing to participate in an audio recorded interview
  • Not able to participate in the interview or complete required study surveys, based on the discretion of the study team

Treatment and study plan

Primary outcomes

  1. Patient perspective on sign, symptoms and impacts of SA-AKI

    Time frame: Up to 3 months

    A 60-min qualitative interview will be conducted and transcripts will be coded to assess which signs, symptoms and impacts of SA-AKI have been experienced by the participant

Secondary outcomes

  1. Patient experiences on treatment pathways and barriers to SA-AKI treatment, the burden of SA-AKI and unmet needs, and the humanistic, societal, and economic impacts

    Time frame: Up to 3 months

    A 60-min qualitative interview will be conducted and transripts will be coded to assess the treatment pathways and barriers to SA-AKI treatment, the burden of SA-AKI and unmet needs, and the humanistic, societal, and economic impacts

Sponsors and collaborators

Lead sponsor

Novartis Pharmaceuticals

Industry

Registry information

Official study title

Concept Elicitation and Patient Experience Mapping in Sepsis-associated Acute Kidney Injury

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Sep 18, 2025
Registry last updated
Dec 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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