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Predicting aspiration pneumonia.

Risk estimation for aspiration pneumonia from known physiological risk factors.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12623001087640
Enrollment
4
Registered
2023-10-17
Start date
2024-09-05
Completion date
2025-06-01
Last updated
2024-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This study will identify whether physiological data collected with clinical information can be used to predict the development of aspiration pneumonia. Additionally, we hypothesize that this information can be used to train a machine learning system for predicting a patient’s risk of developing aspiration pneumonia.

Interventions

Risk factors for the development of aspiration pneumonia will be analyzed. Physiological data taken from all participants will include measures of voluntary and induced cough strength, swallowing-respiratory coordination and indices of oral health (breath analysis). In addition to this, collection of key information from participant medical records will be recorded. Participant involvement will entail approximately 40 minutes of time during one data collection session with a follow-up five minut

Risk factors for the development of aspiration pneumonia will be analyzed. Physiological data taken from all participants will include measures of voluntary and induced cough strength, swallowing-respiratory coordination and indices of oral health (breath analysis). In addition to this, collection of key information from participant medical records will be recorded. Participant involvement will entail approximately 40 minutes of time during one data collection session with a follow-up five minute telephone call three months later for some participants. We have a prototype device that measures swallowing-respiratory coordination, cough strength and oral health.

Sponsors

University of Canterbury
Lead SponsorUniversity

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Patients: Referred to clinicians (e.g. Speech & Language Pathologists) in the Health New Zealand Canterbury region. Able to provide informed consent in isolation or with support of family, friends, and whanau (supported consent). Able to undertake a citric acid cough reflex test (see exclusions below). Healthy aged-matched individuals Able to provide informed consent in isolation or with support of family, friends, and whanau (supported consent). Able to undertake a citric acid cough reflex test (see exclusions below).

Exclusion criteria

Patient exclusion criteria Has a stoma or tracheostomy tube. Is unable to take a cough reflex test. Current diagnosis of pneumonia Has any facial injuries, such as wounds, abrasions, skin allergies or bruising. Has excessive ear wax or other foreign material in ears, an ear infection or inflammation, swelling, or pain in the ear canal. Healthy aged-matched and gender matched individual criteria As per patient exclusion criteria with the addition of: Has a significant disorder, disease, structural or medical abnormality, or injury affecting swallowing or respiration. Has a neurological condition. Has had an upper respiratory tract infection within the last two weeks.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026