Cargando…

Study Protocol: The Norfolk Diabetes Prevention Study [NDPS]: a 46 month multi - centre, randomised, controlled parallel group trial of a lifestyle intervention [with or without additional support from lay lifestyle mentors with Type 2 diabetes] to prevent transition to Type 2 diabetes in high risk groups with non - diabetic hyperglycaemia, or impaired fasting glucose

BACKGROUND: This 7 year NIHR programme [2011–2018] tests the primary hypothesis that the NDPS diet and physical activity intervention will reduce the risk of transition to type 2 diabetes (T2DM) in groups at high risk of Type 2 diabetes. The NDPS programme recognizes the need to reduce intervention...

Descripción completa

Detalles Bibliográficos
Autores principales: Pascale, Melanie, Murray, Nikki, Bachmann, Max, Barton, Garry, Clark, Allan, Howe, Amanda, Greaves, Colin, Sampson, Mike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217324/
https://www.ncbi.nlm.nih.gov/pubmed/28056894
http://dx.doi.org/10.1186/s12889-016-3929-5
_version_ 1782492086424043520
author Pascale, Melanie
Murray, Nikki
Bachmann, Max
Barton, Garry
Clark, Allan
Howe, Amanda
Greaves, Colin
Sampson, Mike
author_facet Pascale, Melanie
Murray, Nikki
Bachmann, Max
Barton, Garry
Clark, Allan
Howe, Amanda
Greaves, Colin
Sampson, Mike
author_sort Pascale, Melanie
collection PubMed
description BACKGROUND: This 7 year NIHR programme [2011–2018] tests the primary hypothesis that the NDPS diet and physical activity intervention will reduce the risk of transition to type 2 diabetes (T2DM) in groups at high risk of Type 2 diabetes. The NDPS programme recognizes the need to reduce intervention costs through group delivery and the use of lay mentors with T2DM, the realities of normal primary care, and the complexity of the current glycaemic categorisation of T2DM risk. METHODS: NDPS identifies people at highest risk of T2DM on the databases of 135 general practices in the East of England for further screening with ab fasting plasma glucose and glycosylated haemoglobin [HbA1c]. Those with an elevated fasting plasma glucose [impaired fasting glucose or IFG] with or without an elevated HbA1c [non -diabetic hyperglycaemia; NDH] are randomised into three treatment arms: a control arm receiving no trial intervention, an arm receiving an intensive bespoke group-based diet and physical activity intervention, and an arm receiving the same intervention with enhanced support from people with T2DM trained as diabetes prevention mentors [DPM]. The primary end point is cumulative transition rates to T2DM between the two intervention groups, and between each intervention group and the control group at 46 months. Participants with screen detected T2DM are randomized into an equivalent prospective controlled trial with the same intervention and control arms with glycaemic control [HbA1c] at 46 months as the primary end point. Participants with NDH and a normal fasting plasma glucose are randomised into an equivalent prospective controlled intervention trial with follow up for 40 months. The intervention comprises six education sessions for the first 12 weeks and then up to 15 maintenance sessions until intervention end, all delivered in groups, with additional support from a DPM in one treatment arm. DISCUSSION: The NDPS programme reports in 2018 and will provide trial outcome data for a group delivered diabetes prevention intervention, supported by lay mentors with T2DM, with intervention in multiple at risk glycaemic categories, and that takes into account the realities of normal clinical practice. TRIAL REGISTRATION: ISRCTN34805606 (Retrospectively registered 16.3.16) ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12889-016-3929-5) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5217324
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-52173242017-01-09 Study Protocol: The Norfolk Diabetes Prevention Study [NDPS]: a 46 month multi - centre, randomised, controlled parallel group trial of a lifestyle intervention [with or without additional support from lay lifestyle mentors with Type 2 diabetes] to prevent transition to Type 2 diabetes in high risk groups with non - diabetic hyperglycaemia, or impaired fasting glucose Pascale, Melanie Murray, Nikki Bachmann, Max Barton, Garry Clark, Allan Howe, Amanda Greaves, Colin Sampson, Mike BMC Public Health Study Protocol BACKGROUND: This 7 year NIHR programme [2011–2018] tests the primary hypothesis that the NDPS diet and physical activity intervention will reduce the risk of transition to type 2 diabetes (T2DM) in groups at high risk of Type 2 diabetes. The NDPS programme recognizes the need to reduce intervention costs through group delivery and the use of lay mentors with T2DM, the realities of normal primary care, and the complexity of the current glycaemic categorisation of T2DM risk. METHODS: NDPS identifies people at highest risk of T2DM on the databases of 135 general practices in the East of England for further screening with ab fasting plasma glucose and glycosylated haemoglobin [HbA1c]. Those with an elevated fasting plasma glucose [impaired fasting glucose or IFG] with or without an elevated HbA1c [non -diabetic hyperglycaemia; NDH] are randomised into three treatment arms: a control arm receiving no trial intervention, an arm receiving an intensive bespoke group-based diet and physical activity intervention, and an arm receiving the same intervention with enhanced support from people with T2DM trained as diabetes prevention mentors [DPM]. The primary end point is cumulative transition rates to T2DM between the two intervention groups, and between each intervention group and the control group at 46 months. Participants with screen detected T2DM are randomized into an equivalent prospective controlled trial with the same intervention and control arms with glycaemic control [HbA1c] at 46 months as the primary end point. Participants with NDH and a normal fasting plasma glucose are randomised into an equivalent prospective controlled intervention trial with follow up for 40 months. The intervention comprises six education sessions for the first 12 weeks and then up to 15 maintenance sessions until intervention end, all delivered in groups, with additional support from a DPM in one treatment arm. DISCUSSION: The NDPS programme reports in 2018 and will provide trial outcome data for a group delivered diabetes prevention intervention, supported by lay mentors with T2DM, with intervention in multiple at risk glycaemic categories, and that takes into account the realities of normal clinical practice. TRIAL REGISTRATION: ISRCTN34805606 (Retrospectively registered 16.3.16) ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12889-016-3929-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-06 /pmc/articles/PMC5217324/ /pubmed/28056894 http://dx.doi.org/10.1186/s12889-016-3929-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Pascale, Melanie
Murray, Nikki
Bachmann, Max
Barton, Garry
Clark, Allan
Howe, Amanda
Greaves, Colin
Sampson, Mike
Study Protocol: The Norfolk Diabetes Prevention Study [NDPS]: a 46 month multi - centre, randomised, controlled parallel group trial of a lifestyle intervention [with or without additional support from lay lifestyle mentors with Type 2 diabetes] to prevent transition to Type 2 diabetes in high risk groups with non - diabetic hyperglycaemia, or impaired fasting glucose
title Study Protocol: The Norfolk Diabetes Prevention Study [NDPS]: a 46 month multi - centre, randomised, controlled parallel group trial of a lifestyle intervention [with or without additional support from lay lifestyle mentors with Type 2 diabetes] to prevent transition to Type 2 diabetes in high risk groups with non - diabetic hyperglycaemia, or impaired fasting glucose
title_full Study Protocol: The Norfolk Diabetes Prevention Study [NDPS]: a 46 month multi - centre, randomised, controlled parallel group trial of a lifestyle intervention [with or without additional support from lay lifestyle mentors with Type 2 diabetes] to prevent transition to Type 2 diabetes in high risk groups with non - diabetic hyperglycaemia, or impaired fasting glucose
title_fullStr Study Protocol: The Norfolk Diabetes Prevention Study [NDPS]: a 46 month multi - centre, randomised, controlled parallel group trial of a lifestyle intervention [with or without additional support from lay lifestyle mentors with Type 2 diabetes] to prevent transition to Type 2 diabetes in high risk groups with non - diabetic hyperglycaemia, or impaired fasting glucose
title_full_unstemmed Study Protocol: The Norfolk Diabetes Prevention Study [NDPS]: a 46 month multi - centre, randomised, controlled parallel group trial of a lifestyle intervention [with or without additional support from lay lifestyle mentors with Type 2 diabetes] to prevent transition to Type 2 diabetes in high risk groups with non - diabetic hyperglycaemia, or impaired fasting glucose
title_short Study Protocol: The Norfolk Diabetes Prevention Study [NDPS]: a 46 month multi - centre, randomised, controlled parallel group trial of a lifestyle intervention [with or without additional support from lay lifestyle mentors with Type 2 diabetes] to prevent transition to Type 2 diabetes in high risk groups with non - diabetic hyperglycaemia, or impaired fasting glucose
title_sort study protocol: the norfolk diabetes prevention study [ndps]: a 46 month multi - centre, randomised, controlled parallel group trial of a lifestyle intervention [with or without additional support from lay lifestyle mentors with type 2 diabetes] to prevent transition to type 2 diabetes in high risk groups with non - diabetic hyperglycaemia, or impaired fasting glucose
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217324/
https://www.ncbi.nlm.nih.gov/pubmed/28056894
http://dx.doi.org/10.1186/s12889-016-3929-5
work_keys_str_mv AT pascalemelanie studyprotocolthenorfolkdiabetespreventionstudyndpsa46monthmulticentrerandomisedcontrolledparallelgrouptrialofalifestyleinterventionwithorwithoutadditionalsupportfromlaylifestylementorswithtype2diabetestopreventtransitiontotype2diabetesinhighriskgroupswith
AT murraynikki studyprotocolthenorfolkdiabetespreventionstudyndpsa46monthmulticentrerandomisedcontrolledparallelgrouptrialofalifestyleinterventionwithorwithoutadditionalsupportfromlaylifestylementorswithtype2diabetestopreventtransitiontotype2diabetesinhighriskgroupswith
AT bachmannmax studyprotocolthenorfolkdiabetespreventionstudyndpsa46monthmulticentrerandomisedcontrolledparallelgrouptrialofalifestyleinterventionwithorwithoutadditionalsupportfromlaylifestylementorswithtype2diabetestopreventtransitiontotype2diabetesinhighriskgroupswith
AT bartongarry studyprotocolthenorfolkdiabetespreventionstudyndpsa46monthmulticentrerandomisedcontrolledparallelgrouptrialofalifestyleinterventionwithorwithoutadditionalsupportfromlaylifestylementorswithtype2diabetestopreventtransitiontotype2diabetesinhighriskgroupswith
AT clarkallan studyprotocolthenorfolkdiabetespreventionstudyndpsa46monthmulticentrerandomisedcontrolledparallelgrouptrialofalifestyleinterventionwithorwithoutadditionalsupportfromlaylifestylementorswithtype2diabetestopreventtransitiontotype2diabetesinhighriskgroupswith
AT howeamanda studyprotocolthenorfolkdiabetespreventionstudyndpsa46monthmulticentrerandomisedcontrolledparallelgrouptrialofalifestyleinterventionwithorwithoutadditionalsupportfromlaylifestylementorswithtype2diabetestopreventtransitiontotype2diabetesinhighriskgroupswith
AT greavescolin studyprotocolthenorfolkdiabetespreventionstudyndpsa46monthmulticentrerandomisedcontrolledparallelgrouptrialofalifestyleinterventionwithorwithoutadditionalsupportfromlaylifestylementorswithtype2diabetestopreventtransitiontotype2diabetesinhighriskgroupswith
AT sampsonmike studyprotocolthenorfolkdiabetespreventionstudyndpsa46monthmulticentrerandomisedcontrolledparallelgrouptrialofalifestyleinterventionwithorwithoutadditionalsupportfromlaylifestylementorswithtype2diabetestopreventtransitiontotype2diabetesinhighriskgroupswith