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The CanCope Study: Comparing the effects of Two Online Wellbeing Programs on the Mental Health of Cancer Survivors

The CanCope Study: A Randomised, Controlled, 8-week, Parallel-group, Superiority Trial to Compare the Efficacy of an Internet-Delivered Transdiagnostic Cognitive Behaviour Therapy to an Internet-Delivered Healthy Lifestyle Intervention for Cancer Survivors

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12620000943943
Enrollment
41
Registered
2020-09-21
Start date
2020-09-24
Completion date
2021-08-21
Last updated
2020-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The purpose of this study is to compare the effects of two internet-delivered interventions on mental health. Who is it for? Eligible participants include adult cancer survivors who have finished their primary treatment for cancer within the last two years. Study details Participants will be randomly selected to take part in one of two interventions: 1. The CanCope Mind intervention, which focuses on helping individuals understand, recognise and respond to uncomfortable emotions, or 2. The CanCope Lifestyle intervention, which focuses on health eating, physical activity, relaxation, and sleep. Both interventions are delivered online over an 8-week period. All participants will need to complete questionnaires during the 8-week period and at 3-months after they have completed the intervention. The findings from this study will inform how to best support the mental health needs of individuals affected by cancer. If effective, the CanCope programs will be one of the few online and easily accessible interventions developed for cancer survivors.

Interventions

Group A: CanCope Mind - Participants randomised to the CanCope Mind condition will receive an 8-week internet-delivered psychological intervention via E-mail links. This intervention is emotion-focused and aims to provide skills to manage emotions more effectively. The intervention comprises 4, 2-week online modules which each include (a) educational reading material, (b) summary videos, and (c) daily online reflection and practical activities, all delivered via REDcap: - Module 1: Focuses on u

Group A: CanCope Mind - Participants randomised to the CanCope Mind condition will receive an 8-week internet-delivered psychological intervention via E-mail links. This intervention is emotion-focused and aims to provide skills to manage emotions more effectively. The intervention comprises 4, 2-week online modules which each include (a) educational reading material, (b) summary videos, and (c) daily online reflection and practical activities, all delivered via REDcap: - Module 1: Focuses on understanding emotions, their components (i.e., thoughts, feelings, behaviours), and their functions. - Module 2: Focuses on building mindfulness skills and involves listening to guided mindfulness audios and practicing techniques to anchor oneself in the present moment. - Module 3: Focuses on building flexible thinking skills (i.e., the ability to challenge negative automatic thoughts and view situations from multiple perspectives). - Module 4: Focuses on identifying and challenging unhelpful emotion-driven behaviours. The internet-delivered intervention is completely standardised and uniform across participants. Participants will receive a brief standardised introductory phone call and an optional mid-program phone call, conducted by a doctoral-level provisional psychologist and trained research assistants. Intervention adherence is assessed by the number of readings and online activities completed.

Sponsors

Monash University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

- Able to read and write in English. - Able to provide informed consent. - Live in Australia, New Zealand, the United Kingdom, the United States of America, or Canada. - Aged >= 18 years. - Previous diagnosis of cancer (any cancer type). - =< 2 years since finishing primary cancer treatment (i.e., surgery, chemotherapy, radiotherapy). - Regular access to the internet and Email. - Regular access to a computer/laptop or Smartphone device.

Exclusion criteria

- Currently undergoing / planning to undergo further primary cancer treatment (i.e., surgery, chemotherapy, radiotherapy). - Endorses current suicidality and considered high risk (assessed in initial phone call) - Current episode of psychosis. - Attending regular sessions with a psychologist or counsellor for their own mental health. - Started or changed psychotropic medication or dose within the previous 2 weeks, or plans to start or change psychotropic medication or dose throughout the 8-week trial.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 12, 2026