このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Holistic Approach Supporting the Uptake of Innovative Diagnostic Technologies for Respiratory Infections (HOLICARE)

2026年8月28日 更新者:Tobias Alfvén、Karolinska Institutet

Clinical Validation of Novel Microfluidic and Lateral Flow-based Technologies for the Detection of Lower and Upper Respiratory Tract Infections - HOLICARE Trial

This observational diagnostic validation study aims to evaluate the clinical performance of novel lateral flow and microfluidic-based technologies for the detection of upper and lower respiratory tract infections in children and adults presenting with respiratory symptoms in Uganda, Ethiopia, and Senegal. The main questions it aims to answer are:

  1. whether the novel multiplex lateral flow tests and point-of-care microfluidic platform demonstrate sufficient sensitivity and specificity for detecting respiratory pathogens compared with standard laboratory reference methods, and
  2. whether these technologies are feasible and usable in low-resource clinical settings.

Participants presenting with suspected respiratory tract infections as part of routine clinical care will provide respiratory and blood samples for diagnostic testing and biobanking, and demographic and clinical information will be collected during a single study visit. Some adult participants and community stakeholders will also complete surveys or interviews regarding the acceptability of biobanking and diagnostic implementation.

調査の概要

詳細な説明

The HOLICARE Clinical Trial (Clinical validation of novel Lateral Flow and microfluidic-based technologies for the detection of Upper and Lower Respiratory Tract Infections) is a multicentre study designed to evaluate innovative point-of-care diagnostic technologies for Respiratory Tract Infections (RTIs). Conducted across 11 clinical sites in Uganda, Senegal, and Ethiopia, the study aims to validate rapid diagnostic tools that can support timely identification and differentiation of viral and bacterial respiratory infections in both primary care and hospital settings. The trial will enrol symptomatic children aged 6 months to 17 years and adults aged 18 years and older presenting with suspected RTIs, including symptoms such as fever, new cough, loss of taste or smell, or fast or difficult breathing.

The objectives for sub-study one are as follows:

Primary objective:

To determine the diagnostic performance, including sensitivity and specificity of the multi-LFT using a nasopharyngeal (NP) swab, with results interpreted via both visual detection and an Android tablet as a reader.

Secondary objective:

  1. To determine the feasibility of using the multi-LFT in primary care settings to provide basic information for rapid screening and triage.
  2. To assess the acceptability of biobanking patient samples for diagnostics and biomedical research through a patient exit/end-of-visit survey [and in-depth semi-structured interviews and focus group discussions] with community stakeholders.
  3. To determine the concordance between results obtained via visual interpretation and the Android tablet application.

The objectives for sub-study 2 can be found below:

Primary objective:

To validate the clinical performance, sensitivity and specificity of a POC platform that performs pathogen detection (bacteria, fungi) using microfluidic Loop-mediated Isothermal Amplification (LAMP) and quantification of host-response biomarkers using a bead-based immunoassay, by comparing its results to those of reference standard methods: benchtop Polymerase Chain Reaction (PCR) and Enzyme Linked Immunosorbent Assay (ELISA), respectively.

Secondary objectives:

  1. To assess whether the POC-Instrument can be inserted in the patient management procedure to assist clinical decision-making.
  2. To assess the hands-on usability of the POC-Instrument and receive feedback by end-users for future implementation in clinical practice.
  3. To assess the acceptability of biobanking patient samples for diagnostics and biomedical research through a patient exit/end-of-visit survey (and in-depth semi-structured interviews and focus group discussions) with community stakeholders.

The study consists of two complementary sub-studies.

Sub-Study 1 focuses on Upper Respiratory Tract Infections (URTIs) and evaluates the diagnostic performance of a multiplex lateral flow test capable of simultaneously detecting Influenza A/B, Respiratory Syncytial Virus (RSV), and COVID-19 from nasopharyngeal swabs. Results will be interpreted both visually and using an Android tablet reader to determine the sensitivity, specificity, and feasibility of the test for rapid screening and triage in primary care settings. Approximately 960 participants will be enrolled to achieve the required number of positive cases for each viral target and to assess concordance between visual and digital interpretation of results.

Sub-Study 2 focuses on Lower Respiratory Tract Infections (LRTIs) and evaluates a novel point-of-care instrument that combines microfluidic Loop-mediated Isothermal amplification (LAMP) for pathogen detection with a bead-based immunoassay to quantify host-response biomarkers. This platform is designed to detect and differentiate targeted bacterial and fungal pathogens while also distinguishing bacterial from non-bacterial infections. The clinical performance of the device will be compared with reference laboratory methods, including PCR and ELISA, in approximately 1,200 participants.

Participants will be recruited at participating hospitals and health centres and must present with at least two respiratory tract infection symptoms during screening. Participation will not alter routine clinical care, and eligible patients will provide written informed consent (or assent with parental/guardian consent for children). For Sub-Study 1, sample collection includes two nasopharyngeal swabs for lateral flow testing and an additional swab for PCR analysis. For Sub-Study 2, sputum is the primary sample collected, with bronchoalveolar lavage samples obtained from a limited number of patients where clinically appropriate. If sputum or BAL samples cannot be obtained, a nasopharyngeal swab may be collected as an alternative for testing on the point-of-care instrument. Saliva and blood samples will also be collected for biobanking to support future diagnostic and biomedical research in both sub-studies. In addition to evaluating clinical performance, the study will assess the usability of the diagnostic technologies, their integration into clinical workflows, and the acceptability of sample biobanking among patients and community stakeholders.

研究の種類

観察的

入学 (実際)

1765

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Mbarara、ウガンダ
        • Epicentre Mbarara Research Centre
      • Addis Ababa、エチオピア
        • Armauer Hansen Research Institute (AHRI)
      • Dakar、セネガル
        • Institut Pasteur de Dakar

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

サンプリング方法

非確率サンプル

調査対象母集団

The study will enrol symptomatic children aged 6 months to 17 years and adults aged ≥18 years of both sexes presenting to participating hospitals and health centres with suspected upper or lower respiratory tract infections (RTIs). Participants will be recruited in Uganda, Ethiopia, and Senegal from outpatient and inpatient healthcare settings. Eligible participants will present with at least two symptoms consistent with respiratory infection, such as fever, acute cough, shortness of breath, tachypnoea, or loss of smell and/or taste. Participants (or parents/guardians for minors) will provide written informed consent prior to enrolment.

説明

Inclusion Criteria:

  • Age ≥ 6 months
  • Presentation with suspected respiratory tract infection and at least two of the following symptoms:
  • Fever (axillary temperature ≥37.5°C) or history of fever
  • New acute cough episode
  • Shortness of breath
  • Tachypnoea (fast breathing)
  • Loss of smell and/or taste
  • Ability to provide written informed consent (or assent with parent/guardian consent for minors)
  • For infants (≤1 year), both fever and new acute cough must be present at screening

Exclusion Criteria:

  • Refusal or inability to provide informed consent/assent
  • Refusal to provide study samples
  • Severe chronic medical conditions or mental incapacity that, in the opinion of the clinician, would interfere with study participation
  • Hospitalisation within the previous 2 weeks for reasons unrelated to the current respiratory symptoms
  • Acute injury, trauma, or poisoning interfering with participation
  • Chronic cough lasting >2 weeks, unless tuberculosis is suspected in the LRTI cohort
  • Antibiotic use within the previous 2 weeks for participants enrolled in the LRTI cohort (Sub-study 2) only

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Upper respiratory tract infections (URTIs) cohort (sub-study 1)
時間枠:From April 2025 to May 2026
To determine the diagnostic performance, including sensitivity and specificity of the multi-LFT using a nasopharyngeal (NP) swab, with results interpreted via both visual detection and an Android tablet as a reader.
From April 2025 to May 2026

二次結果の測定

結果測定
メジャーの説明
時間枠
Lower Respiratory Tract Infections - Point-of-Care Instrument cohort (sub-study 2)
時間枠:April 2025 to May 2026
To validate the clinical performance (sensitivity and specificity) of a POC platform that performs pathogen detection (bacteria, fungi) using microfluidic-LAMP isothermal amplification and quantification of host-response biomarkers, using a bead-based immunoassay, by comparing its results to those of reference standard methods (benchtop PCR and ELISA, respectively).
April 2025 to May 2026

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • スタディチェア:Aman Russom, PhD、KTH Royal Institute of Technology
  • 主任研究者:Juliet Mwanga-Amumpaire, MD, PhD、Epicentre Mbarara Research Centre
  • 主任研究者:Adane Mihret, DVM, MSc, PhD、Armauer Hansen Research Institute, Ethiopia
  • 主任研究者:Cheikh Fall, PhD、Institut Pasteur de Dakar

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2025年4月7日

一次修了 (実際)

2026年8月28日

研究の完了 (実際)

2026年8月28日

試験登録日

最初に提出

2026年6月11日

QC基準を満たした最初の提出物

2026年6月11日

最初の投稿 (実際)

2026年6月16日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月1日

QC基準を満たした最後の更新が送信されました

2026年8月28日

最終確認日

2026年6月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • 101057596 (その他の助成金/資金番号:European Commission Horizon Program)
  • 10049786 (その他の識別子:UK Research and Innovations)
  • SEN24/10 (その他の識別子:Comité National d'Ethique pour la Recherche en Santé (CNERS))
  • PO-01-23 (その他の識別子:Ethiopias' National Health & Research Ethics)
  • HS3718ES (その他の識別子:Uganda National Council for Science & Technology)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • ICF
  • CSR

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する