Canine COVID-19 Detection Phase 2 and 3 (LSH1394)

Arctec

Status: Unknown

Conditions: SARS-CoV2 Infection; Covid19

Treatments: Behavioral: Testing with medical detection dogs

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT04948190

LSH1394

Details and patient eligibility

About

The purpose of this study is to determine whether trained medical detection dogs can accurately detect the presence of COVID-19 in people infected with the virus, or using samples of their clothing or body odour.

The study will train dogs to identify and discriminate between individuals wearing clothing collected from people infected with SARS-CoV-2 and uninfected individuals under semi-field conditions.Following this training, field testing will be used to determine whether trained dogs can distinguish between people infected with SARS-CoV-2 and uninfected individuals, producing estimates of dogs' sensitivity and specificity.

Full description

When the COVID-19 epidemic wanes it will be important to prevent outbreaks of, and the reintroduction of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) into the country, since there will be many susceptible individuals remaining in the population. In order to prevent third and further waves of COVID-19, it will be important to screen passengers arriving from high-risk countries. This task would be made simpler if a rapid non-invasive method were available for detecting infected individuals, particularly those with asymptomatic, pre-symptomatic or prodromal symptomatic infections with SARS-CoV-2 from those individuals who are not carrying the virus.

Thermal screening, practised in many airports and ports around the world, has a low sensitivity since not all patients develop fever. Consequently, it has received considerable criticism in some quarters. The use of trained dogs could provide a rapid primary screen for detecting those potentially carrying the SARS-CoV-2 virus. Travellers indicated by the dogs as likely to be carrying the virus would then be tested by nasal and throat swabs, with diagnosis confirmed/excluded using real-time RT-PCR or an accurate rapid diagnostic test according to Government Guidelines. Using trained dogs would enable extremely rapid screening, with each dog able to assess up to 250 travellers per hour, saving time and money.

There is evidence that viral and bacterial respiratory infections cause the release of specific odours from human cells. Other work with detection dogs has found dogs can detect and learn the smell of virus-associated volatiles in real time, with sensitivities of up to 96% and specificity of up to 98%. The current study will build further investigate whether trained dogs can differentiate between odours associated with viral infections.

In Phase 1 of this study (Clinical Trials ref: NCT04509713), the investigators hypothesised that dogs, with their highly advanced sense of smell could be trained to detect people infected with the SARS-CoV-2 virus. Medical Detection Dogs were trained and tested using stand trials with clothing samples worn by people who had variously tested positive or negative for SARS-CoV-2 in RT-PCR tests.

In Phase 2, the clothing collected in Phase 1 will be used to train and transition the dogs from Phase 1, where they identified samples in the laboratory environment, to semi-field settings. Phase 1 clothing samples will be worn by human volunteers in a series of 'line-up' trials, under increasingly complex settings. As part of phase 2, study staff will opportunistically conduct line-up tests with volunteers confirmed to be infected with SARS-CoV-2, to allow dogs to learn the whole-body odour of infection.

Phase 3 will take place once the investigators have demonstrated the dogs can work within a real-world environment (Phase 2 above). In this phase, trainers will deploy the dogs and evaluate performance through in use testing. This will be done at a suitable venue, most likely a COVID-19 testing centre, airport or university, to ensure a high enough rate of potential positive individuals.

Enrollment: 11,015 estimated patients

Sex: All

Ages: 16+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Phase 2, training part 1 & 2

• Adult male or female, aged 16 years or over.
• Written (hard copy or electronic) or verbal informed consent provided.
• Willing and able to wear or carry clothing (e.g. t-shirt) collected as part of Phase 1 from an individual infected with SARS-CoV-2 or an individual not infected with SARS-CoV-2.
• Has declared non-symptomatic 7 days (as defined by the latest NHS guidance) prior to participation in the training exercise.
• Would be willing to have a SARS-CoV-2 test within 24 h of the training exercise if required.

Phase 2, training part 3

• Adult male or female, aged 16 years or over.
• Written (hard copy or electronic) or verbal informed consent provided.
• Has received a positive result for SARS-CoV-2 from a test conducted within the past 5 days. or is experiencing SARS-CoV-2 symptoms.
• Willing and able to share, or grant access to, their SARS-CoV-2 test result.
• Has access to private outdoor space (e.g. front garden, driveway), reachable without leaving the location where the participant is self-isolating.
• Is asymptomatic or mildly ill (i.e. not requiring hospitalisation, able to walk short distances and stand for up to 15 minutes).

Phase 2 part 4, acceptability and feasibility study

• Adult male or female, aged 16 years or over.
• Written (hard copy or electronic) or verbal informed consent provided.
• Would be willing to have a SARS-CoV-2 test within 72 hours of the training exercise if required.
• Willing and able to share, or grant access to their SARS-CoV-2 test result.

Phase 2 part 5, Criteria for all volunteers

• Adult male or female, aged 16 years or over
• Electronic informed consent provided

Additional criteria for volunteers participating in focus groups

• Adult male or female, aged 16 years or over.
• Written (hard copy or electronic) or verbal informed consent provided.
• Able to access online video-conferencing tools (such as Zoom or Teams).

Phase 3, Deployment testing

• Adult male or female, aged 16 years or over.
• Willing and able to have a SARS-CoV-2 test within 96 h of participation in the deployment exercise.
• Willing and able to share, or grant access to, their SARS-CoV-2 test result.
• Verbal or written (hard copy or electronic) informed consent provided by the participant.

Exclusion criteria

Phase 2, training part 1 & 2

• Younger than 16 years old
• Informed consent not provided
• Unwilling or unable to wear or carry clothing from an individual infected or uninfected with SARS-CoV-2.
• Has not declared non-symptomatic within 7 days prior to the training exercise.
• Is unwilling or unable to have a SARS-CoV-2 test within 24 hours of the training exercise if required.

Phase 2, training part 3

• Adult male or female, aged under 16 years.
• Informed consent not provided.
• Has not received a positive result for SARS-CoV-2 or experiencing SARS-CoV-2 symptoms.
• Unwilling or unable to share, or grant access to their SARS-CoV-2 test result.
• Has no access to private outdoor space.
• Participant requires hospitalisation or is unable to walk short distances and stand for up to 15 minutes.

Phase 2 part 4, acceptability and feasibility study

• Adult male or female, aged under 16 years.
• Informed consent not provided.
• Unwilling or unable to have a SARS-CoV-2 test within 72 hours of the training exercise if required.
• Unwilling or unable to share, or grant access to their SARS-CoV-2 test result. Phase 2 part 5 Criteria for all volunteers
• Adult male or female, aged under 16 years.
• Informed consent not provided Additional criteria for volunteers participating in focus groups.
• Adult male or female, aged under 16 years · Informed consent not provided.
• Unable to access online video-conferencing tools (such as Zoom or Teams)

Phase 3 Deployment testing

• Adult male or female, aged under 16 years
• Informed consent not provided.
• Unwilling or unable to have a SARS-CoV-2 test within 96 hours of participation in the deployment exercise.
• Unwilling or unable to provide a scent swab.
• Unwilling or unable to share, or grant access to, their SARS-CoV-2 test result.

Trial design

11,015 participants in 2 patient groups

SARS-CoV-2 Infected/ positive group

Description:

Has tested positive for SARS-CoV-2 within appropriate timeframe (criteria vary for different study stages). Aged 16 years or older, willing and able to provide informed consent.

Treatment:

Behavioral: Testing with medical detection dogs

SARS-CoV-2 negative group

Description:

Has tested negative for SARS-CoV-2 within appropriate timeframe (criteria vary for different study stages, and in phase 2 part 1, 2 and 4 enrolment may be accepted using symptoms-based criteria). Aged 16 years or older, willing and able to provide informed consent.

Treatment:

Behavioral: Testing with medical detection dogs