Multi-center, pragmatic, cluster-randomized, controlled trial of standardized peritoneal dialysis (PD) training versus usual care on PD-related infections (the TEACH-PD trial): trial protocol.

Cluster randomized controlled trial Competency assessment Cost-effectiveness Outcomes Patient education Peritoneal dialysis Peritonitis Standardized training

Journal

Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253

Informations de publication

Date de publication:
14 Nov 2023
Historique:
received: 30 05 2023
accepted: 07 10 2023
medline: 15 11 2023
pubmed: 15 11 2023
entrez: 15 11 2023
Statut: epublish

Résumé

Peritoneal dialysis (PD)-related infections, such as peritonitis, exit site, and tunnel infections, substantially impair the sustainability of PD. Accordingly, PD-related infection is the top-priority research outcome for patients and caregivers. While PD nurse trainers teach patients to perform their own PD, PD training curricula are not standardized or informed by an evidentiary base and may offer a potential approach to prevent PD infections. The Targeted Education ApproaCH to improve Peritoneal Dialysis outcomes (TEACH-PD) trial evaluates whether a standardized training curriculum for PD nurse trainers and incident PD patients based on the International Society for Peritoneal Dialysis (ISPD) guidelines reduces PD-related infections compared to usual training practices. The TEACH-PD trial is a registry-based, pragmatic, open-label, multi-center, binational, cluster-randomized controlled trial. TEACH-PD will recruit adults aged 18 years or older who have not previously undergone PD training at 42 PD treatment units (clusters) in Australia and New Zealand (ANZ) between July 2019 and June 2023. Clusters will be randomized 1:1 to standardized TEACH-PD training curriculum or usual training practice. The primary trial outcome is the time to the first occurrence of any PD-related infection (exit site infection, tunnel infection, or peritonitis). The secondary trial outcomes are the individual components of the primary outcome, infection-associated catheter removal, transfer to hemodialysis (greater than 30 days and 180 days), quality of life, hospitalization, all-cause death, a composite of transfer to hemodialysis or all-cause death, and cost-effectiveness. Participants are followed for a minimum of 12 months with a targeted average follow-up period of 2 years. Participant and outcome data are collected from the ANZ Dialysis and Transplant Registry (ANZDATA) and the New Zealand Peritoneal Dialysis (NZPD) Registry. This protocol follows the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) guidelines. TEACH-PD is a registry-based, cluster-randomized pragmatic trial that aims to provide high-certainty evidence about whether an ISPD guideline-informed standardized PD training curriculum for PD nurse trainers and adult patients prevents PD-related infections. ClinicalTrials.gov NCT03816111. Registered on 24 January 2019.

Sections du résumé

BACKGROUND BACKGROUND
Peritoneal dialysis (PD)-related infections, such as peritonitis, exit site, and tunnel infections, substantially impair the sustainability of PD. Accordingly, PD-related infection is the top-priority research outcome for patients and caregivers. While PD nurse trainers teach patients to perform their own PD, PD training curricula are not standardized or informed by an evidentiary base and may offer a potential approach to prevent PD infections. The Targeted Education ApproaCH to improve Peritoneal Dialysis outcomes (TEACH-PD) trial evaluates whether a standardized training curriculum for PD nurse trainers and incident PD patients based on the International Society for Peritoneal Dialysis (ISPD) guidelines reduces PD-related infections compared to usual training practices.
METHODS METHODS
The TEACH-PD trial is a registry-based, pragmatic, open-label, multi-center, binational, cluster-randomized controlled trial. TEACH-PD will recruit adults aged 18 years or older who have not previously undergone PD training at 42 PD treatment units (clusters) in Australia and New Zealand (ANZ) between July 2019 and June 2023. Clusters will be randomized 1:1 to standardized TEACH-PD training curriculum or usual training practice. The primary trial outcome is the time to the first occurrence of any PD-related infection (exit site infection, tunnel infection, or peritonitis). The secondary trial outcomes are the individual components of the primary outcome, infection-associated catheter removal, transfer to hemodialysis (greater than 30 days and 180 days), quality of life, hospitalization, all-cause death, a composite of transfer to hemodialysis or all-cause death, and cost-effectiveness. Participants are followed for a minimum of 12 months with a targeted average follow-up period of 2 years. Participant and outcome data are collected from the ANZ Dialysis and Transplant Registry (ANZDATA) and the New Zealand Peritoneal Dialysis (NZPD) Registry. This protocol follows the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) guidelines.
DISCUSSION CONCLUSIONS
TEACH-PD is a registry-based, cluster-randomized pragmatic trial that aims to provide high-certainty evidence about whether an ISPD guideline-informed standardized PD training curriculum for PD nurse trainers and adult patients prevents PD-related infections.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov NCT03816111. Registered on 24 January 2019.

Identifiants

pubmed: 37964367
doi: 10.1186/s13063-023-07715-0
pii: 10.1186/s13063-023-07715-0
pmc: PMC10647147
doi:

Banques de données

ClinicalTrials.gov
['NCT03816111']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

730

Subventions

Organisme : National Health and Medical Research Council
ID : APP1170238
Organisme : National Health and Medical Research Council
ID : APP1092957
Organisme : Health Research Council of New Zealand
ID : 19/290

Informations de copyright

© 2023. Crown.

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Auteurs

Josephine S F Chow (JSF)

South Western Sydney Local Health District, Liverpool, NSW, Australia. Josephine.Chow@health.nsw.gov.au.
Ingham Institute for Applied Medical Research, Liverpool, NSW, Australia. Josephine.Chow@health.nsw.gov.au.
University of New South Wales, Kennington, NSW, Australia. Josephine.Chow@health.nsw.gov.au.
Western Sydney University, Sydney, NSW, Australia. Josephine.Chow@health.nsw.gov.au.
University of Tasmania, Hobart, TAS, Australia. Josephine.Chow@health.nsw.gov.au.

Neil Boudville (N)

Medical School, University of Western Australia, Crawley, WA, Australia.
Department of Renal Medicine, Sir Charles Gairdner Hospital, Nedlands, WA, Australia.

Yeoungjee Cho (Y)

Department of Kidney and Transplant Service, Princess Alexandra Hospital, Brisbane, QLD, Australia.
Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Suetonia Palmer (S)

Department of Medicine, University of Otago, Christchurch, New Zealand.
Te Whatu Ora Health New Zealand, Hamilton, New Zealand.

Elaine M Pascoe (EM)

Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Carmel M Hawley (CM)

Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.
Translational Research Institute, Brisbane, QLD, Australia.
Metro South Kidney and Transplant Service, Princess Alexandra Hospital, Brisbane, QLD, Australia.

Donna M Reidlinger (DM)

Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Laura E Hickey (LE)

Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Ruth Stastny (R)

Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Andrea Valks (A)

Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Liza Vergara (L)

Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Ramya Movva (R)

Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Charani Kiriwandeniya (C)

Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Hayley Candler (H)

Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Gabor Mihala (G)

Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Bernadette Buisman (B)

Health New Zealand, Te Whatu Ora Te Tai Tokerau, Hamilton, New Zealand.
University of Auckland, Te Tai Tokerau Northtec, Auckland, New Zealand.

Keri-Lu Equinox (KL)

Cairns Hospital, Cairns, QLD, Australia.

Ana E Figueiredo (AE)

School of Nursing, Escola de Ciências da Saúde E da Vida, Pontifícia Universidade Católica Do Rio Grande Do Sul, Porto Alegre, Brazil.

Trudi Fuge (T)

, Wollongong, Australia.

Kirsten Howard (K)

Sydney School of Public Health, The University of Sydney, Sydney, NSW, Australia.
Menzies Centre for Health Policy and Economics, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.

Martin Howell (M)

Menzies Centre for Health Policy and Economics, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.

Allison Jaure (A)

Sydney School of Public Health, The University of Sydney, Sydney, NSW, Australia.

Matthew D Jose (MD)

University of Tasmania, Hobart, TAS, Australia.
Renal Unit, Royal Hobart Hospital, Hobart, TAS, Australia.

Anna Lee (A)

, Shoalhaven, Australia.

Susana S Miguel (SS)

South Western Sydney Local Health District, Liverpool, NSW, Australia.
Ingham Institute for Applied Medical Research, Liverpool, NSW, Australia.

Jo-Anne Moodie (JA)

Royal Melbourne Hospital, Parkville, VIC, Australia.

Thu T Nguyen (TT)

Health New Zealand, Te Whatu Ora Te Toka Tumai, Hamilton, New Zealand.

Geraldine Pinlac (G)

Department of Medicine, University of Otago, Christchurch, New Zealand.

Annie Reynolds (A)

Health New Zealand, Te Whatu Ora Te Matua a Māui Hawkes Bay, Hamilton, New Zealand.

Walaa W M Saweirs (WWM)

Health New Zealand, Te Whatu Ora Te Tai Tokerau, Hamilton, New Zealand.

Genevieve Z Steiner-Lim (GZ)

NICM Health Research Institute, Western Sydney University Sydney, Campbelltown, NSW, Australia.

Bronwen TeWhare (B)

Health New Zealand, Te Whatu Ora Taranaki, Hamilton, New Zealand.

Melinda Tomlins (M)

Department of Nephrology, Hunter New England Local Health District, New Lambton, NSW, Australia.

Megan Upjohn (M)

Health New Zealand, Te Whatu Ora Te Toka Tumai, Hamilton, New Zealand.

David Voss (D)

Health New Zealand, Te Whatu Ora Counties Manukau, Hamilton, New Zealand.

Rachael C Walker (RC)

Te Pukenga Eastern Institute of Technology, Christchurch, New Zealand.

Joanne Wilson (J)

Department of Medicine, University of Otago, Christchurch, New Zealand.

David W Johnson (DW)

Department of Kidney and Transplant Service, Princess Alexandra Hospital, Brisbane, QLD, Australia.
Australasian Kidney Trials Network, Centre for Health Services Research, The University of Queensland, Brisbane, QLD, Australia.

Classifications MeSH