The main aim of the current study is to investigate whether the addition of a standardized,group-based educational program to the information provided by health care personnel improves cancer patients' knowledge level about their disease, planned treatment and common side-effects of the treatment. Secondary aims are to investigate if the addition of the educational program increases the likelihood of completing treatment as planned, reduces level of anxiety, reduces the frequency of serious side effects, increases patient reported health related quality of life, and increases the degree of patient satisfaction with respect to how they have received the information before, during and after treatment.
There are strong indications that group-based information provides better information for cancer patients about their disease, treatment options - and potential benefits and side effects of the planned therapy than information provided during a regular doctor consultation. The investigators believe that standardizing and repeating the information as well as having more time for questions in an open environment for reflections will improve the amount of information patients can perceive. Furthermore, all patients will be given written information. Better-informed patients may be more motivated and may contact health care personnel earlier than other patients when they develop side effects. This may reduce the risk of serious treatment-related complications and increase the chances of patients completing the planned treatment. But none have compared to what extent an organization like Vardesenteret improves the patients' knowledge and whether patients are more satisfied with these methods for informing them. Results from studies on the influence of patient anxiety and distress on patient's abilities to perceive information are conflicting.Two large groups of relatively homogenous cancer patients are patients with lower-stage breast cancer patients who are eligible for adjuvant chemotherapy and patients with localized prostate cancer eligible for curative radiotherapy.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
98
The patients will receive two 1.5-2 hour standardized validated group information sessions in addition to regular information from their doctors and nurses.
St Olavs Hospital
Trondheim, Norway
Knowledge
Knowledge questionnaires specially made for the study. Constructed as statements with response categories; correct, false and don´t know.
Time frame: 1 week
Knowledge
Knowledge questionnaires specially made for the study. Constructed as statements with response categories; correct, false and don´t know.
Time frame: 2 weeks
Knowledge
Knowledge questionnaires specially made for the study. Constructed as statements with response categories; correct, false and don´t know.
Time frame: 9 weeks
Quality of Life
European Organization for Research and Treatment of Cancer Core Quality-of-Life Questionnaire C30
Time frame: 9 weeks
Patients Subjective state of information
European Organization for Research and Treatment of Cancer Core Quality-of-Life Questionnaire INFO 25
Time frame: 1 week
Patients Subjective state of information
European Organization for Research and Treatment of Cancer Core Quality-of-Life Questionnaire INFO 25
Time frame: 2 weeks
Patients Subjective state of information
European Organization for Research and Treatment of Cancer Core Quality-of-Life Questionnaire INFO 25
Time frame: 9 weeks
Anxiety
STAI-State and Trait Anxiety Inventory
Time frame: 1 week
Anxiety
STAI-State and Trait Anxiety Inventory
Time frame: 2 weeks
Anxiety
STAI-State and Trait Anxiety Inventory
Time frame: 9 weeks
Adverse events
CTCEA, Common Terminology Criteria for Adverse Events
Time frame: 2 weeks
Adverse events
CTCEA, Common Terminology Criteria for Adverse Events
Time frame: 9 weeks
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