Early Rehabilitation of Cancer Patients

Haukeland University Hospital

Status: Completed

Conditions: Breast Cancer; Testicle Cancer; Lymphoma; Prostate Cancer; Colorectal Cancer

Treatments: Other: Stressmanagement

Study type: Interventional

Funder types: Other

Identifiers

NCT01588262

REKnr 2010/1911

Details and patient eligibility

About

A life threatening disease such as cancer may lead to post traumatic stress disorder, and even when reporting low levels of side-effects from cancer disease and treatment, 80% report high levels of stress symptoms. The purpose of the present randomised controlled trial is to examine the psychosocial effects of a stress management intervention based on cognitive behaviour therapy and with focus on increased physical activity in patients with various cancer diagnoses using a stepped-care approach. When using a stepped-care approach it is possible to study the level and intensity of stress management intervention required to achieve increased well-being. A cost-utility analysis will also be performed. 300 adult patients with a recent diagnosis of breast-, colorectal- prostate, testicular cancer or lymphoma and scheduled for adjuvant and/or curative oncologic treatment at Haukeland University Hospital, will be consecutively included in the prospective intervention study. The patients will be randomized to intervention or control. In step 1, all patients in the intervention group (I-a) will receive 2 counselling sessions. Patients who report clinically significant levels of stress, such as intrusive thoughts/avoidance behaviour (measured by Impact of Event Scale) and/or worry and depressions (measured by Hospital and Depression Scale) will be included in Step 2 (I-b) and include another 4-7 counselling sessions. There will also be a focus on motivating to increase physical activity level. Both the intervention (I) and control group (C) are allowed to take part in the common rehabilitation program with patient education and physical training. Data will be collected with self-reported standardized questionnaires. Objectively measures of physical activity level, sleep and daily energy expenditure are recorded with SenseWear™ Pro3 Armband. Measure point is at inclusion and than after 6 week, 4, 8, 12 and 24 month.

Enrollment: 300 patients

Sex: All

Ages: 18 to 81 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Newly diagnosed with breast cancer,
• colorectal cancer,
• lymphoma,
• prostate cancer or testicle cancer and scheduled for adjuvant and/or curative treatment in the form of chemotherapy, radiation therapy and/or hormonal therapy at the Department of Oncology and Medical physics, Haukeland University Hospital, (Dept. of Oncology) Bergen,
• residence in Rogaland, Hordaland and Sogn and fjordane county council,
• initial treatment for cancer

Exclusion criteria

• An ongoing psychiatric condition,
• language deficiencies in Norwegian,
• surgery for prostate cancer (only applies for prostate cancer) patients),
• men with breast cancer,
• live in nursing homes,
• previous cancer,
• treated for cancer earlier,
• already implemented oncological treatment,
• not self-reliant

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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300 participants in 2 patient groups

Stressmanagement counselling

Other group

Treatment:

Other: Stressmanagement

Control

No Intervention group