The All Ireland Infectious Diseases Cohort Project
AIID
1 other identifier
observational
10,000
1 country
9
Brief Summary
The All-Ireland Infectious Diseases (AIID) Cohort is a multicentre, prospective, longitudinal observational cohort that enrols consecutive adult subjects attending participating institutions for infectious disease services. This is an ongoing prospective observational cohort of unlimited duration.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2011
Longer than P75 for all trials
9 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2011
CompletedFirst Submitted
Initial submission to the registry
April 5, 2023
CompletedFirst Posted
Study publicly available on registry
May 10, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2024
CompletedMay 10, 2024
May 1, 2024
13.8 years
April 5, 2023
May 8, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Establishment of data rich cohort
Overall number of recruited participants and number of recruited participants with major conditions (COVID-19, HIV, TB)
through study completion, an average of 1 year
Secondary Outcomes (2)
Cohort retention
through study completion, an average of 1 year
Cohort associated metadata
through study completion, an average of 1 year
Eligibility Criteria
All adult patients attending Clinical Services relating to infectious diseases at participating hospitals in Ireland who provide written informed consent.
You may qualify if:
- ≥ 18 years of age patients attending clinical services of participating institutions with issues related to infectious diseases.
- Willing and able to provide informed consent or
- Provide deferred assent if an incapacitated or unconscious patient is unable to provide informed consent
You may not qualify if:
- Patients under 18 years of age
- Patients with learning disabilities, mental illness, or dementia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University College Dublinlead
- Beaumont Hospitalcollaborator
- Children's Health Irelandcollaborator
- Cork University Hospitalcollaborator
- Mater Misericordiae University Hospitalcollaborator
- Our Lady of Lourdes Hospital, Droghedacollaborator
- St. James's Hospital, Irelandcollaborator
- St. Luke's Hospital, Irelandcollaborator
- St Vincent's University Hospital, Irelandcollaborator
- Wexford General Hospitalcollaborator
Study Sites (9)
Cork University Hospital
Cork, Ireland
Our Lady of Lourdes Hospital, Drogheda
Drogheda, Ireland
St Vincent's University Hospital, Ireland
Dublin, D4, Ireland
Mater Misericordiae University Hospital
Dublin, Dublin 7, Ireland
Beaumont Hospital
Dublin, Ireland
Children's Health Ireland at Crumlin
Dublin, Ireland
St James's Hospital
Dublin, Ireland
St Luke's General Hospital, Kilkenny
Kilkenny, Ireland
Wexford General Hospital
Wexford, Ireland
Related Links
Biospecimen
1. Blood sample to be prepared as plasma, serum and viable peripheral blood mononuclear cells (PBMC) for cryopreservation. 2. Respiratory samples (where relevant e.g., subject with respiratory viral infection or pulmonary TB) 3. Stool sample for later microbiome analysis (optional) 4. Urine 5. Swabs, including mucosal (e.g., ano-genital, naso-pharyngeal) and superficial (skin). In addition, where subjects undergo lumbar puncture testing as part of routine care, any excess available sample may also be stored. These stored samples provide the opportunity for future research studies investigating host factors associated with the response to infection.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Patrick Mallon, PhD, FRCPI
UCD
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 5, 2023
First Posted
May 10, 2024
Study Start
March 1, 2011
Primary Completion
December 1, 2024
Study Completion
December 1, 2024
Last Updated
May 10, 2024
Record last verified: 2024-05