A randomised controlled trial of a tele-based lifestyle intervention for colorectal cancer survivors ('CanChange'): study protocol
<p>Abstract</p> <p>Background</p> <p>Colorectal cancer survivors may suffer from a range of ongoing psychosocial and physical problems that negatively impact on quality of life. This paper presents the study protocol for a novel telephone-delivered intervention to impro...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
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BMC
2009-08-01
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Series: | BMC Cancer |
Online Access: | http://www.biomedcentral.com/1471-2407/9/286 |
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author | Gordon Louisa G Baade Peter Gollschewski Sara Courneya Kerry S Pakenham Kenneth I Hawkes Anna L Lynch Brigid M Aitken Joanne F Chambers Suzanne K |
author_facet | Gordon Louisa G Baade Peter Gollschewski Sara Courneya Kerry S Pakenham Kenneth I Hawkes Anna L Lynch Brigid M Aitken Joanne F Chambers Suzanne K |
author_sort | Gordon Louisa G |
collection | DOAJ |
description | <p>Abstract</p> <p>Background</p> <p>Colorectal cancer survivors may suffer from a range of ongoing psychosocial and physical problems that negatively impact on quality of life. This paper presents the study protocol for a novel telephone-delivered intervention to improve lifestyle factors and health outcomes for colorectal cancer survivors.</p> <p>Methods/Design</p> <p>Approximately 350 recently diagnosed colorectal cancer survivors will be recruited through the Queensland Cancer Registry and randomised to the intervention or control condition. The intervention focuses on symptom management, lifestyle and psychosocial support to assist participants to make improvements in lifestyle factors (physical activity, healthy diet, weight management, and smoking cessation) and health outcomes. Participants will receive up to 11 telephone-delivered sessions over a 6 month period from a qualified health professional or 'health coach'. Data collection will occur at baseline (Time 1), post-intervention or six months follow-up (Time 2), and at 12 months follow-up for longer term effects (Time 3). Primary outcome measures will include physical activity, cancer-related fatigue and quality of life. A cost-effective analysis of the costs and outcomes for survivors in the intervention and control conditions will be conducted from the perspective of health care costs to the government.</p> <p>Discussion</p> <p>The study will provide valuable information about an innovative intervention to improve lifestyle factors and health outcomes for colorectal cancer survivors.</p> <p>Trial Registration</p> <p>ACTRN12608000399392</p> |
first_indexed | 2024-04-13T00:34:39Z |
format | Article |
id | doaj.art-96c1d3471d974587abd1c473f9dcc151 |
institution | Directory Open Access Journal |
issn | 1471-2407 |
language | English |
last_indexed | 2024-04-13T00:34:39Z |
publishDate | 2009-08-01 |
publisher | BMC |
record_format | Article |
series | BMC Cancer |
spelling | doaj.art-96c1d3471d974587abd1c473f9dcc1512022-12-22T03:10:21ZengBMCBMC Cancer1471-24072009-08-019128610.1186/1471-2407-9-286A randomised controlled trial of a tele-based lifestyle intervention for colorectal cancer survivors ('CanChange'): study protocolGordon Louisa GBaade PeterGollschewski SaraCourneya Kerry SPakenham Kenneth IHawkes Anna LLynch Brigid MAitken Joanne FChambers Suzanne K<p>Abstract</p> <p>Background</p> <p>Colorectal cancer survivors may suffer from a range of ongoing psychosocial and physical problems that negatively impact on quality of life. This paper presents the study protocol for a novel telephone-delivered intervention to improve lifestyle factors and health outcomes for colorectal cancer survivors.</p> <p>Methods/Design</p> <p>Approximately 350 recently diagnosed colorectal cancer survivors will be recruited through the Queensland Cancer Registry and randomised to the intervention or control condition. The intervention focuses on symptom management, lifestyle and psychosocial support to assist participants to make improvements in lifestyle factors (physical activity, healthy diet, weight management, and smoking cessation) and health outcomes. Participants will receive up to 11 telephone-delivered sessions over a 6 month period from a qualified health professional or 'health coach'. Data collection will occur at baseline (Time 1), post-intervention or six months follow-up (Time 2), and at 12 months follow-up for longer term effects (Time 3). Primary outcome measures will include physical activity, cancer-related fatigue and quality of life. A cost-effective analysis of the costs and outcomes for survivors in the intervention and control conditions will be conducted from the perspective of health care costs to the government.</p> <p>Discussion</p> <p>The study will provide valuable information about an innovative intervention to improve lifestyle factors and health outcomes for colorectal cancer survivors.</p> <p>Trial Registration</p> <p>ACTRN12608000399392</p>http://www.biomedcentral.com/1471-2407/9/286 |
spellingShingle | Gordon Louisa G Baade Peter Gollschewski Sara Courneya Kerry S Pakenham Kenneth I Hawkes Anna L Lynch Brigid M Aitken Joanne F Chambers Suzanne K A randomised controlled trial of a tele-based lifestyle intervention for colorectal cancer survivors ('CanChange'): study protocol BMC Cancer |
title | A randomised controlled trial of a tele-based lifestyle intervention for colorectal cancer survivors ('CanChange'): study protocol |
title_full | A randomised controlled trial of a tele-based lifestyle intervention for colorectal cancer survivors ('CanChange'): study protocol |
title_fullStr | A randomised controlled trial of a tele-based lifestyle intervention for colorectal cancer survivors ('CanChange'): study protocol |
title_full_unstemmed | A randomised controlled trial of a tele-based lifestyle intervention for colorectal cancer survivors ('CanChange'): study protocol |
title_short | A randomised controlled trial of a tele-based lifestyle intervention for colorectal cancer survivors ('CanChange'): study protocol |
title_sort | randomised controlled trial of a tele based lifestyle intervention for colorectal cancer survivors canchange study protocol |
url | http://www.biomedcentral.com/1471-2407/9/286 |
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