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NCT Number: NCT07029672

The AcCREDiT 2 Study

The ACCREDIT study - Acute respiratory infections and chronic respiratory disease exacerbations characterisation and personalised treatment platform study 2 (AcCREDiT 2).

Patients with respiratory infections (such as pneumonia) or exacerbations of chronic respiratory conditions (such as emphysema) often require hospital admission. Infections or exacerbation are commonly caused by bacteria, viruses or fungi. In at least a quarter of patients no infectious cause of the exacerbation is found. Depending on the cause of the respiratory infections or exacerbations of chronic respiratory condition patients require prompt treatment with anti-infective drugs (antibiotics, anti-fungal or antiviral drugs) or anti-inflammatory drugs such as corticosteroids.

Patients with respiratory infection or exacerbations of chronic respiratory conditions develop symptoms such as cough, sometimes with sputum, fever or breathlessness. These symptoms can be similar across several conditions, many of which are not due to infection (for example heart failure or blood clots in the lungs). When assessing patients with respiratory symptoms, clinicians face the challenge of limited information in the early stages of care as it takes three days to identify infectious organisms in the laboratory. Even when an infection is strongly suspected, distinguishing bacterial from viral or fungal infections on clinical grounds alone is difficult. This uncertainty often leads clinicians to prescribe a number of treatments, including antibiotics, before a clear diagnosis is made. Timely treatment is crucial for success and improved patient outcomes, especially for critically ill patients admitted to the intensive care unit (ICU). However, antibiotics may cause side effects, such as sickness and diarrhoea, and overuse of antibiotics leads to antibiotic resistance, making antibiotics less effective when they are really needed. Giving antibiotics to patients with an infection or exacerbation and avoiding antibiotics in patients without an infection requires rapid diagnostic tests. Furthermore, giving antibiotics prior to taking samples to diagnose infection can affect the sample being tested making it more likely to not give a useful result. For a diagnostic test for infection to be most useful it needs to be collected before an antibiotic is given - this is true for both clinical tests and those research tests which are clinical tests in development.

Modern technologies allow testing for an infection in hours rather than days. In order to understand how effective these technologies are, samples need to be taken from patients before they start treatment. In routine NHS care samples to test for infection should be taken before treatment has been started. However, in research studies samples are often taken up to a day after treatment has started which affects how effective the test is at finding infection. The forerunner to this study, called AcCREDiT, proposed investigating very rapid ways of identifying individuals with respiratory infection and exacerbation. However, the study team encountered challenges during the informed consent process, particularly with acutely unwell patients. Therefore, the AcCREDiT-2 was designed in collaboration with patients and public contributors to look at the feasibility of a modified informed consent process: verbal consent, assent for individuals with capacity to consent for themselves, and deferred consent.

AcCREDiT-2 will be an observational study, meaning that no treatment will be changed, and no experimental drugs or tests used to influence the clinical care of participants. AcCREDiT-2 will also be a 'feasibility study', which is a smaller study designed to see what works well before embarking on a larger project. During the study the investigators will collect clinical information and samples, such as blood, sputum and stool, from patients who come to hospital with a presumed respiratory infection or exacerbation of their chronic respiratory condition. The investigators will compare new diagnostic tests to traditional laboratory tests to understand their relative advantages and disadvantages for patient care.

This is a 'feasibility' study, a small study ran first to make sure things work properly before expanding to a much larger study.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years
  • Clinically suspected acute respiratory infection or exacerbation of chronic respiratory disease
  • Availability of respiratory tract sample
  • Spontaneously breathing patients are able to produce a sputum sample
  • Mechanically ventilated patients in intensive care are due to have an Bronchoalveolar lavage or non-directed bronchial lavage for a clinical indication
  • Due to receive either:
  • an anti-infective agent (e.g. antibiotic, antiviral or antifungal) OR
  • a systemic anti-inflammatory agent (e.g. corticosteroid)
  • Valid informed consent, assent or enrolment through deferred consent
  • Re-enrolment will be allowed if presenting for a separate acute event

Exclusion criteria

  • Alternate respiratory cause of presentation in the opinion of the treating physician (e.g. pulmonary embolism, heart failure, etc.)
  • High clinical likelihood of infection with a Hazard Group 3 pathogen (e.g. tuberculosis, anthrax, plague)

Treatment and study plan

Primary outcomes

  1. Feasibility of timely recruitment, assessment, and retention during follow up

    Time frame: 12 months

    Endpoints: Number of patients recruited within 12 months of study start, recruitment expected at a minimum of 2 patients per week enrolled into the study, feasibility attainment target: 120 patients across different clinical environments and diagnostic categories.

Secondary outcomes

  1. Efficacy of verbal consent

    Time frame: 12 months

    Feasibility of study - Proportion of patients declining consent at verbal consent stage

  2. Efficacy of 'consent to continue' model following verbal consent

    Time frame: 12 months

    Measure of study feasibility - Proportion of patients voluntarily withdrawing from study following verbal consent

  3. Availability of respiratory tract samples and stool samples for analysis

    Time frame: 12 months

    Measure of study feasibility - Proportion of patients in whom sputum and/or stool samples are successfully obtained for analysis

  4. Infectious aetiology of presentation

    Time frame: 12 months

    Measure of study feasibility - Proportion of patients presenting with bacterial infection, viral infection, fungal infection, or no identifiable infective causes

  5. Diagnostic categorisation of patients recruited

    Time frame: 12 months

    Study feasibility assessment - Proportion of patients presenting with prespecified diagnoses (e.g. pneumonia, exacerbation of COPD)

  6. Performance of different diagnostic strategies

    Time frame: 12 months

    Measure of study feasibility - Comparison of results from routine microbiological approaches (service standard) with molecular techniques to identify pathogens.

  7. Impact of delayed sampling on diagnosis and prescribing of antibiotics

    Time frame: 12 months

    Comparison of results from blood and sputum samples taken prior to treatment being commenced with samples collected 3-6 hours after treatment has been commenced.

  8. Hospital length of stay (days)

    Time frame: 12 months

    Number of days from hospital admission to discharge - informing feasibility of study and future study

  9. ICU length of stay, if admitted (days)

    Time frame: 12 months

    Number of days from ICU admission to discharge to inform feasibility of future study and recruitment methods

  10. 28-day mortality

    Time frame: 12 months

    Proportion of patients alive at 28 days from enrolment - feasibility of study and recruitment methods

Study contacts

Contact information is provided by the study sponsor or research team.

Luke Ward

CONTACT

[email protected]

0161 291 5757

Tim Felton

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Manchester University NHS Foundation Trust

Other Gov

Registry information

Official study title

Acute Respiratory Infections and Chronic Respiratory Disease Exacerbation Characterisation and Personalised Treatment Platform Study 2

Acronym: ACCREDIT2

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 19, 2025
Registry last updated
Jul 4, 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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