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Improving Vitamin D Status and Related Health in Young Women: The Safe-D study – Part B
BACKGROUND: Vitamin D deficiency is highly prevalent and associated with increased risk of a number of chronic health conditions including cardiovascular disease, poor bone and muscle health, poor mental health, infection, and diabetes. Vitamin D deficiency affects millions of Australians, potential...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JMIR Publications Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879332/ https://www.ncbi.nlm.nih.gov/pubmed/27166214 http://dx.doi.org/10.2196/resprot.5465 |
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author | Tabesh, Marjan Garland, Suzanne Marie Gorelik, Alexandra Nankervis, Alison Maclean, Skye Callegari, Emma Teresa Chang, Shanton Heffernan, Kayla Wark, John Dennis |
author_facet | Tabesh, Marjan Garland, Suzanne Marie Gorelik, Alexandra Nankervis, Alison Maclean, Skye Callegari, Emma Teresa Chang, Shanton Heffernan, Kayla Wark, John Dennis |
author_sort | Tabesh, Marjan |
collection | PubMed |
description | BACKGROUND: Vitamin D deficiency is highly prevalent and associated with increased risk of a number of chronic health conditions including cardiovascular disease, poor bone and muscle health, poor mental health, infection, and diabetes. Vitamin D deficiency affects millions of Australians, potentially causing considerable suffering, economic loss, and mortality. OBJECTIVE: To measure the effectiveness of a (1) mobile-based app (behavioral) and (2) pharmacological intervention to increase circulating 25-hydroxyvitamin D (serum 25 OHD) levels and health outcomes over 4 months of intervention compared with usual care in a cohort of young women with suboptimal serum 25 OHD levels (25-75 nmol/L). METHODS: Participants with 25 OHD levels 25 to 75 nmol/L are invited to participate in this study. Participants are randomized to one of three groups in 1:1:1 ratio: a mobile phone–based application, vitamin D supplementation (1000 IU/day), and a control group. Data collection points are at baseline, 4, and 12 months post baseline with the major endpoints being at 4 months. A wide-range of information is collected from participants throughout the course of this study. General health, behavioral and demographic information, medications, smoking, alcohol and other substance use, health risk factors, nutrition, eating patterns and disorders, and mental health data are sourced from self-administered, Web-based surveys. Clinical data include anthropometric measurements, a silicone skin cast of the hand, cutaneous melanin density, bone mineral density, and body composition scans obtained through site visits. Main analyses will be conducted in two ways on an intention-to-treat (ITT) basis using the last observation carried forward approach as an imputation for missing data, and on a per protocol basis to compare the intervention arms against the control group at 4 and 12 months. RESULTS: Publication of trial results is anticipated in 2017. CONCLUSIONS: The study will allow assessment of the effects of a mobile-based app behavioral intervention and vitamin D supplementation on vitamin D status and will evaluate the effects of improving vitamin D levels on several health outcomes. |
format | Online Article Text |
id | pubmed-4879332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | JMIR Publications Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48793322016-06-08 Improving Vitamin D Status and Related Health in Young Women: The Safe-D study – Part B Tabesh, Marjan Garland, Suzanne Marie Gorelik, Alexandra Nankervis, Alison Maclean, Skye Callegari, Emma Teresa Chang, Shanton Heffernan, Kayla Wark, John Dennis JMIR Res Protoc Protocol BACKGROUND: Vitamin D deficiency is highly prevalent and associated with increased risk of a number of chronic health conditions including cardiovascular disease, poor bone and muscle health, poor mental health, infection, and diabetes. Vitamin D deficiency affects millions of Australians, potentially causing considerable suffering, economic loss, and mortality. OBJECTIVE: To measure the effectiveness of a (1) mobile-based app (behavioral) and (2) pharmacological intervention to increase circulating 25-hydroxyvitamin D (serum 25 OHD) levels and health outcomes over 4 months of intervention compared with usual care in a cohort of young women with suboptimal serum 25 OHD levels (25-75 nmol/L). METHODS: Participants with 25 OHD levels 25 to 75 nmol/L are invited to participate in this study. Participants are randomized to one of three groups in 1:1:1 ratio: a mobile phone–based application, vitamin D supplementation (1000 IU/day), and a control group. Data collection points are at baseline, 4, and 12 months post baseline with the major endpoints being at 4 months. A wide-range of information is collected from participants throughout the course of this study. General health, behavioral and demographic information, medications, smoking, alcohol and other substance use, health risk factors, nutrition, eating patterns and disorders, and mental health data are sourced from self-administered, Web-based surveys. Clinical data include anthropometric measurements, a silicone skin cast of the hand, cutaneous melanin density, bone mineral density, and body composition scans obtained through site visits. Main analyses will be conducted in two ways on an intention-to-treat (ITT) basis using the last observation carried forward approach as an imputation for missing data, and on a per protocol basis to compare the intervention arms against the control group at 4 and 12 months. RESULTS: Publication of trial results is anticipated in 2017. CONCLUSIONS: The study will allow assessment of the effects of a mobile-based app behavioral intervention and vitamin D supplementation on vitamin D status and will evaluate the effects of improving vitamin D levels on several health outcomes. JMIR Publications Inc. 2016-05-10 /pmc/articles/PMC4879332/ /pubmed/27166214 http://dx.doi.org/10.2196/resprot.5465 Text en ©Marjan Tabesh, Suzanne Marie Garland, Alexandra Gorelik, Alison Nankervis, Skye Maclean, Emma Teresa Callegari, Shanton Chang, Kayla Heffernan, John Dennis Wark. Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 10.05.2016. https://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/ (https://creativecommons.org/licenses/by/2.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Research Protocols, is properly cited. The complete bibliographic information, a link to the original publication on http://www.researchprotocols.org, as well as this copyright and license information must be included. |
spellingShingle | Protocol Tabesh, Marjan Garland, Suzanne Marie Gorelik, Alexandra Nankervis, Alison Maclean, Skye Callegari, Emma Teresa Chang, Shanton Heffernan, Kayla Wark, John Dennis Improving Vitamin D Status and Related Health in Young Women: The Safe-D study – Part B |
title | Improving Vitamin D Status and Related Health in Young Women: The Safe-D study – Part B |
title_full | Improving Vitamin D Status and Related Health in Young Women: The Safe-D study – Part B |
title_fullStr | Improving Vitamin D Status and Related Health in Young Women: The Safe-D study – Part B |
title_full_unstemmed | Improving Vitamin D Status and Related Health in Young Women: The Safe-D study – Part B |
title_short | Improving Vitamin D Status and Related Health in Young Women: The Safe-D study – Part B |
title_sort | improving vitamin d status and related health in young women: the safe-d study – part b |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879332/ https://www.ncbi.nlm.nih.gov/pubmed/27166214 http://dx.doi.org/10.2196/resprot.5465 |
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