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Coping-Together: A feasibility study of a novel, self-directed supportive care intervention to enhance illness adjustment of couples affected by prostate cancer.

A randomised controlled study of the illness adjustment of couples affected by prostate cancer using 'Coping- Together', a self-directed supportive care intervention, compared to couples receiving minimal ethical care.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000438954
Acronym
PAct: Partners in Action
Enrollment
200
Registered
2011-04-28
Start date
2012-02-20
Completion date
2013-05-30
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This study aims to test the feasibility of providing a Coping-Together self-directed supportive care intervention to couples affected by prostate cancer. It is anticipated that using the proposed Coping-Together skills will be primarily associated with couples experiencing less anxiety. Who is it for? You may be eligible for this study if you have recently been diagnosed with a primary, early-stage prostate cancer, are currently receiving or planning to receive treatment, gain a score of 4 or above on a Distress Thermometer (DT) measurement, have a partner who is willing to participate in the study, and you are both able to understand and complete feedback surveys on your level of care and support. Trial Details: You will be randomised to one of two treatment arms in this study, either the Coping-Together (CT) arm, or to the Minimal Ethical Care (MEC) arm. The purpose of this study is to test which arm works better in couples to enhance your illness adjustment, along with how well the two of you are able to cope with your illness. Both arms involve being supplied with cancer and coping information; all or some of which you can use at your own pace. You will also receive fortnightly follow-up phone calls from research staff over a 2 month period following baseline measurements.

Interventions

Coping-Together takes on a holistic approach to coping with cancer by including strategies to manage physical, social, psychological, and existential cancer-related challenges. The key component of Coping-Together is a series of four booklets, which translate the most up-to-date research on effective, practical coping strategies and render it readily available to couples. Each booklet addresses one of the following challenges: 1) symptom management, 2) communicating effectively with health care

Coping-Together takes on a holistic approach to coping with cancer by including strategies to manage physical, social, psychological, and existential cancer-related challenges. The key component of Coping-Together is a series of four booklets, which translate the most up-to-date research on effective, practical coping strategies and render it readily available to couples. Each booklet addresses one of the following challenges: 1) symptom management, 2) communicating effectively with health care professionals, 3) supporting your partner, and 4) managing worries and emotions. For each challenge, specific coping strategies are proposed, including a step-by-step guide to mindfulness and muscle relaxation, practical self-care tips to manage side effects, using a question prompt list to improve communication with health care professionals, and worksheets to encourage joint problem-solving. Multiple coping strategies are presented to couples to facilitate a personalised approach, where couples can ‘pick and choose’ and apply those that most closely correspond to their needs. Also, the booklets contain information about additional health care resources that can contribute to optimal coping and illness adjustment, including the type of support that can be expected from different members of their health care team. The Coping-Together booklets are complemented by electronic media, including a relaxation CD and 'coping coach' DVD, which features content from the ‘communicating effectively with health care professionals’ booklet. Participants will be able to use any or all of these resources at their own discretion and pace prior to collection of the outcome data, which will be 2 months following baseline measurements.

Sponsors

The University of New South Wales, Faculty of Medicine, South Western Sydney Clinical School, Ingham Institute for Applied Medical Research
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used)

Eligibility

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

Inclusion criteria

a) Recently diagnosed with a primary, early-stage prostate cancer, b) Receiving/planning to receive treatment, c) Score 4+ on Distress Thermometer (DT), d) Partner willing to participate in the study, and e) Sufficiently fluent in English and cognitively able to complete surveys.

Exclusion criteria

Identified by health care professionals as not being well enough to participate in study, which might include, but is not limited to, concurrent psychiatric conditions. Partner not willing to participate.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 25, 2026