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A study protocol for a randomised controlled trial of an interactive web-based intervention: CancerCope
INTRODUCTION: Approximately 35% of patients with cancer experience clinically significant distress, and unmet psychological supportive care needs are prevalent. This study describes the protocol for a randomised controlled trial (RCT) to assess the efficacy and cost-effectiveness of an internet-base...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541614/ https://www.ncbi.nlm.nih.gov/pubmed/28645985 http://dx.doi.org/10.1136/bmjopen-2017-017279 |
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author | Chambers, Suzanne K Ritterband, Lee Thorndike, Frances Nielsen, Lisa Aitken, Joanne F Clutton, Samantha Scuffham, Paul Youl, Philippa Morris, Bronwyn Baade, Peter Dunn, Jeffrey |
author_facet | Chambers, Suzanne K Ritterband, Lee Thorndike, Frances Nielsen, Lisa Aitken, Joanne F Clutton, Samantha Scuffham, Paul Youl, Philippa Morris, Bronwyn Baade, Peter Dunn, Jeffrey |
author_sort | Chambers, Suzanne K |
collection | PubMed |
description | INTRODUCTION: Approximately 35% of patients with cancer experience clinically significant distress, and unmet psychological supportive care needs are prevalent. This study describes the protocol for a randomised controlled trial (RCT) to assess the efficacy and cost-effectiveness of an internet-based psychological intervention for distressed patients with cancer. METHODS AND ANALYSIS: In phase I, the intervention was developed on an interactive web platform and pilot tested for acceptability using a qualitative methodology with 21 patients with cancer. Phase II is an RCT underway with patients with or at risk of elevated psychological distress comparing: (1) static patient education website with (2) individualised web-delivered cognitive behavioural intervention (CancerCope). Participants were recruited through the Queensland Cancer Registry and Cancer Council Helpline and met the following inclusion criteria: (1) recently diagnosed with cancer; (2) able to read and speak English; (3) no previous history of head injury, dementia or psychiatric illness; (4) no other concurrent cancer; (5) phone and internet access; (5) scored ≥4 on the Distress Thermometer. Participants are assessed at four time points: baseline/recruitment and 2, 6 and 12 months after recruitment and intervention commencement. Of the 163 participants recruited, 50% met caseness for distress. The area of highest unmet supportive care needs were psychological followed by physical and daily living needs. Primary outcomes are psychological and cancer-specific distress and unmet psychological supportive care needs. Secondary outcomes are positive adjustment, quality of life and cost-effectiveness. ETHICS AND DISSEMINATION: Ethical approval was obtained from the Griffith University Human Research Ethics Committee (Approval: PSY/70/13/HREC) and the Metro South Human Research Ethics Committee (HREC/13/QPAH/601). All participants provide informed consent prior to taking part in the study. Once completed, this study will provide recommendations about the efficacy of web-based cognitive behavioural interventions to facilitate better psychosocial adjustment for people with cancer. TRIAL REGISTRATION NUMBER: ANZCTR (ACTRN12613001026718). |
format | Online Article Text |
id | pubmed-5541614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55416142017-08-07 A study protocol for a randomised controlled trial of an interactive web-based intervention: CancerCope Chambers, Suzanne K Ritterband, Lee Thorndike, Frances Nielsen, Lisa Aitken, Joanne F Clutton, Samantha Scuffham, Paul Youl, Philippa Morris, Bronwyn Baade, Peter Dunn, Jeffrey BMJ Open Oncology INTRODUCTION: Approximately 35% of patients with cancer experience clinically significant distress, and unmet psychological supportive care needs are prevalent. This study describes the protocol for a randomised controlled trial (RCT) to assess the efficacy and cost-effectiveness of an internet-based psychological intervention for distressed patients with cancer. METHODS AND ANALYSIS: In phase I, the intervention was developed on an interactive web platform and pilot tested for acceptability using a qualitative methodology with 21 patients with cancer. Phase II is an RCT underway with patients with or at risk of elevated psychological distress comparing: (1) static patient education website with (2) individualised web-delivered cognitive behavioural intervention (CancerCope). Participants were recruited through the Queensland Cancer Registry and Cancer Council Helpline and met the following inclusion criteria: (1) recently diagnosed with cancer; (2) able to read and speak English; (3) no previous history of head injury, dementia or psychiatric illness; (4) no other concurrent cancer; (5) phone and internet access; (5) scored ≥4 on the Distress Thermometer. Participants are assessed at four time points: baseline/recruitment and 2, 6 and 12 months after recruitment and intervention commencement. Of the 163 participants recruited, 50% met caseness for distress. The area of highest unmet supportive care needs were psychological followed by physical and daily living needs. Primary outcomes are psychological and cancer-specific distress and unmet psychological supportive care needs. Secondary outcomes are positive adjustment, quality of life and cost-effectiveness. ETHICS AND DISSEMINATION: Ethical approval was obtained from the Griffith University Human Research Ethics Committee (Approval: PSY/70/13/HREC) and the Metro South Human Research Ethics Committee (HREC/13/QPAH/601). All participants provide informed consent prior to taking part in the study. Once completed, this study will provide recommendations about the efficacy of web-based cognitive behavioural interventions to facilitate better psychosocial adjustment for people with cancer. TRIAL REGISTRATION NUMBER: ANZCTR (ACTRN12613001026718). BMJ Publishing Group 2017-06-23 /pmc/articles/PMC5541614/ /pubmed/28645985 http://dx.doi.org/10.1136/bmjopen-2017-017279 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Oncology Chambers, Suzanne K Ritterband, Lee Thorndike, Frances Nielsen, Lisa Aitken, Joanne F Clutton, Samantha Scuffham, Paul Youl, Philippa Morris, Bronwyn Baade, Peter Dunn, Jeffrey A study protocol for a randomised controlled trial of an interactive web-based intervention: CancerCope |
title | A study protocol for a randomised controlled trial of an interactive web-based intervention: CancerCope |
title_full | A study protocol for a randomised controlled trial of an interactive web-based intervention: CancerCope |
title_fullStr | A study protocol for a randomised controlled trial of an interactive web-based intervention: CancerCope |
title_full_unstemmed | A study protocol for a randomised controlled trial of an interactive web-based intervention: CancerCope |
title_short | A study protocol for a randomised controlled trial of an interactive web-based intervention: CancerCope |
title_sort | study protocol for a randomised controlled trial of an interactive web-based intervention: cancercope |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541614/ https://www.ncbi.nlm.nih.gov/pubmed/28645985 http://dx.doi.org/10.1136/bmjopen-2017-017279 |
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