None listed
Conditions
Brief summary
The aim of this study is to assess the efficacy and cost-effectiveness of an interactive web-based psychological intervention for people with cancer and elevated psychological distress. Who is it for? Participants will be identified through notifications received by the Queensland Cancer Registry (QCR), or be referred through Cancer Council's Information and Support service 131120. Participants will be aged 18 years or above, live in Queensland, have been diagnosed with malignant melanoma or colorectal cancer within the past 6 months (QCR) OR have been diagnosed with cancer (131120), are experiencing elevated psychological distress and have phone and internet access. Study details Participants in this study will be randomly (by chance) allocated to one of two groups. Participants in one group will have access to an interactive, individualised, internet based cognitive behavioural intervention. The intervention aims to provide information and support to patients, to help them adjust to a diagnosis of cancer and reduce their cancer-related distress. The intervention will include educational information and videos with self-management tools and interactive tasks tailored in response to users' needs as determined by their input. Participants in the other group will receive access to a static education website, containing information on stress management skills, problem solving approaches to cancer-related concerns, and patient education about a healthy lifestyle to promote wellness and optimise quality of life. All participants will be asked to complete a number of questionnaires at baseline, 2, 6, and 12 months, in order to assess their psychological distress and quality of life.
Interventions
Interactive, individualised, internet based cognitive behavioural intervention. The intervention aims to provide information and support to patients, to help them adjust to a diagnosis of cancer and reduce their cancer-related distress. Topics will include stress reduction, problem-solving, cognitive challenging and enhancing relationship support. To deliver the psychological intervention, the application will include educational information and videos with self-management tools and interactive tasks tailored in response to users' needs as determined by their input. The program has high levels of interactivity - self-assessment and monitoring tools such as quizzes and online diaries - to increase user engagement and systems to encourage use and self-management including personalised email reminders, follow up and feedback. The intervention will consist of six cores and will be metered (distributed), rather than provided all at once (like a static health information website). Cores one and two will be available immediately after completion of baseline assessment. Subsequent cores (three through to six) will be released at seven day intervals. Participants will be encouraged to complete the core within seven days of its release. It is anticipated that each core will take approximately one hour to complete. In addition to the six cores, the participant will have access to a “library” of information relevant to various challenges associated with cancer (e.g., managing fatigue, coping with treatment, managing conflict with a loved one). Following completion of all six cores, participants will be encouraged to review the core information and utilise the “library”. Participants will receive continued access to the intervention for the duration of the twelve month intervention period, to be accessed at their discretion.
Sponsors
Study design
Eligibility
Inclusion criteria
1) have been recently diagnosed with invasive melanoma or invasive colorectal cancer (patients will be within six months of diagnosis at recruitment)(QCR recruitment) OR be diagnosed with cancer (131120 recruitment); 2) be able to read and speak English; 3) have no previous history of head injury, dementia or psychiatric illness; 4) have no other concurrent cancer; 5) have phone and internet access; 6) have physician clearance to participate in the study (QCR recruitment only); 7) score 4 or higher on the Distress Thermometer (indicating high distress, or at risk of high distress)
Exclusion criteria
1) Children and/or young people (ie. <18 years) 2) People with an intellectual or mental impairment