Cargando…
A tailored lifestyle intervention to reduce the cardiovascular disease risk of individuals with Familial Hypercholesterolemia (FH): design of the PRO-FIT randomised controlled trial
BACKGROUND: Because of a high cardiovascular disease (CVD) risk in people with Familial Hypercholesterolemia (FH), early prevention of cardiovascular disease is important for health gain and cost reduction. This project focuses on the development and evaluation of an innovative intervention aiming t...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2834628/ https://www.ncbi.nlm.nih.gov/pubmed/20156339 http://dx.doi.org/10.1186/1471-2458-10-69 |
_version_ | 1782178584147787776 |
---|---|
author | Broekhuizen, Karen van Poppel, Mireille NM Koppes, Lando LJ Brug, Johannes van Mechelen, Willem |
author_facet | Broekhuizen, Karen van Poppel, Mireille NM Koppes, Lando LJ Brug, Johannes van Mechelen, Willem |
author_sort | Broekhuizen, Karen |
collection | PubMed |
description | BACKGROUND: Because of a high cardiovascular disease (CVD) risk in people with Familial Hypercholesterolemia (FH), early prevention of cardiovascular disease is important for health gain and cost reduction. This project focuses on the development and evaluation of an innovative intervention aiming to reduce CVD risk by promoting a healthy lifestyle among people with FH. METHODS: This project is designed as a randomised controlled trial in which individuals with FH will be assigned randomly to a control or intervention group. In the intervention group (n = 200), participants will receive a personalized intervention which is a combination of web-based tailored lifestyle advice and personal counselling by a lifestyle coach. The control group (n = 200) will receive care as usual. Primary outcomes are biological indicators of CVD risk: systolic blood pressure, glucose, BMI, waist circumference and lipids (triglycerides, total, LDL and HDL cholesterol). Secondary outcomes are: healthy lifestyle behaviour (with regard to smoking, physical activity, dietary pattern and compliance to statin therapy) and psychological correlates and determinants of healthy lifestyle behaviour (knowledge, attitude, risk perception, social influence, self-efficacy, cues to action, intention and autonomy). Measurement will take place at baseline, and at 3 and 12 months after randomisation. Additionally, a throughout process-evaluation will be conducted to assess and monitor intervention implementation during the trial. DISCUSSION: Results of the PRO-FIT project will provide information about the effects and implementation of a healthy lifestyle intervention for individuals with FH. Our experiences with this intervention will be indicative about the suitability, feasibility and benefits of this approach for future interventions in other high-risk groups, such as Familial Combined Hypercholesterolemia (FCH) and diabetes. TRIAL REGISTRATION NUMBER: NTR1899 |
format | Text |
id | pubmed-2834628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28346282010-03-09 A tailored lifestyle intervention to reduce the cardiovascular disease risk of individuals with Familial Hypercholesterolemia (FH): design of the PRO-FIT randomised controlled trial Broekhuizen, Karen van Poppel, Mireille NM Koppes, Lando LJ Brug, Johannes van Mechelen, Willem BMC Public Health Study protocol BACKGROUND: Because of a high cardiovascular disease (CVD) risk in people with Familial Hypercholesterolemia (FH), early prevention of cardiovascular disease is important for health gain and cost reduction. This project focuses on the development and evaluation of an innovative intervention aiming to reduce CVD risk by promoting a healthy lifestyle among people with FH. METHODS: This project is designed as a randomised controlled trial in which individuals with FH will be assigned randomly to a control or intervention group. In the intervention group (n = 200), participants will receive a personalized intervention which is a combination of web-based tailored lifestyle advice and personal counselling by a lifestyle coach. The control group (n = 200) will receive care as usual. Primary outcomes are biological indicators of CVD risk: systolic blood pressure, glucose, BMI, waist circumference and lipids (triglycerides, total, LDL and HDL cholesterol). Secondary outcomes are: healthy lifestyle behaviour (with regard to smoking, physical activity, dietary pattern and compliance to statin therapy) and psychological correlates and determinants of healthy lifestyle behaviour (knowledge, attitude, risk perception, social influence, self-efficacy, cues to action, intention and autonomy). Measurement will take place at baseline, and at 3 and 12 months after randomisation. Additionally, a throughout process-evaluation will be conducted to assess and monitor intervention implementation during the trial. DISCUSSION: Results of the PRO-FIT project will provide information about the effects and implementation of a healthy lifestyle intervention for individuals with FH. Our experiences with this intervention will be indicative about the suitability, feasibility and benefits of this approach for future interventions in other high-risk groups, such as Familial Combined Hypercholesterolemia (FCH) and diabetes. TRIAL REGISTRATION NUMBER: NTR1899 BioMed Central 2010-02-15 /pmc/articles/PMC2834628/ /pubmed/20156339 http://dx.doi.org/10.1186/1471-2458-10-69 Text en Copyright ©2010 Broekhuizen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Study protocol Broekhuizen, Karen van Poppel, Mireille NM Koppes, Lando LJ Brug, Johannes van Mechelen, Willem A tailored lifestyle intervention to reduce the cardiovascular disease risk of individuals with Familial Hypercholesterolemia (FH): design of the PRO-FIT randomised controlled trial |
title | A tailored lifestyle intervention to reduce the cardiovascular disease risk of individuals with Familial Hypercholesterolemia (FH): design of the PRO-FIT randomised controlled trial |
title_full | A tailored lifestyle intervention to reduce the cardiovascular disease risk of individuals with Familial Hypercholesterolemia (FH): design of the PRO-FIT randomised controlled trial |
title_fullStr | A tailored lifestyle intervention to reduce the cardiovascular disease risk of individuals with Familial Hypercholesterolemia (FH): design of the PRO-FIT randomised controlled trial |
title_full_unstemmed | A tailored lifestyle intervention to reduce the cardiovascular disease risk of individuals with Familial Hypercholesterolemia (FH): design of the PRO-FIT randomised controlled trial |
title_short | A tailored lifestyle intervention to reduce the cardiovascular disease risk of individuals with Familial Hypercholesterolemia (FH): design of the PRO-FIT randomised controlled trial |
title_sort | tailored lifestyle intervention to reduce the cardiovascular disease risk of individuals with familial hypercholesterolemia (fh): design of the pro-fit randomised controlled trial |
topic | Study protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2834628/ https://www.ncbi.nlm.nih.gov/pubmed/20156339 http://dx.doi.org/10.1186/1471-2458-10-69 |
work_keys_str_mv | AT broekhuizenkaren atailoredlifestyleinterventiontoreducethecardiovasculardiseaseriskofindividualswithfamilialhypercholesterolemiafhdesignoftheprofitrandomisedcontrolledtrial AT vanpoppelmireillenm atailoredlifestyleinterventiontoreducethecardiovasculardiseaseriskofindividualswithfamilialhypercholesterolemiafhdesignoftheprofitrandomisedcontrolledtrial AT koppeslandolj atailoredlifestyleinterventiontoreducethecardiovasculardiseaseriskofindividualswithfamilialhypercholesterolemiafhdesignoftheprofitrandomisedcontrolledtrial AT brugjohannes atailoredlifestyleinterventiontoreducethecardiovasculardiseaseriskofindividualswithfamilialhypercholesterolemiafhdesignoftheprofitrandomisedcontrolledtrial AT vanmechelenwillem atailoredlifestyleinterventiontoreducethecardiovasculardiseaseriskofindividualswithfamilialhypercholesterolemiafhdesignoftheprofitrandomisedcontrolledtrial AT broekhuizenkaren tailoredlifestyleinterventiontoreducethecardiovasculardiseaseriskofindividualswithfamilialhypercholesterolemiafhdesignoftheprofitrandomisedcontrolledtrial AT vanpoppelmireillenm tailoredlifestyleinterventiontoreducethecardiovasculardiseaseriskofindividualswithfamilialhypercholesterolemiafhdesignoftheprofitrandomisedcontrolledtrial AT koppeslandolj tailoredlifestyleinterventiontoreducethecardiovasculardiseaseriskofindividualswithfamilialhypercholesterolemiafhdesignoftheprofitrandomisedcontrolledtrial AT brugjohannes tailoredlifestyleinterventiontoreducethecardiovasculardiseaseriskofindividualswithfamilialhypercholesterolemiafhdesignoftheprofitrandomisedcontrolledtrial AT vanmechelenwillem tailoredlifestyleinterventiontoreducethecardiovasculardiseaseriskofindividualswithfamilialhypercholesterolemiafhdesignoftheprofitrandomisedcontrolledtrial |