A prospective study to a blended ACT e-health training in curative treated breastcancer patients with distress: results and patient reports.
Completed
- Conditions
- distress-klachtendistressfeeling uncomfortable
- Registration Number
- NL-OMON44742
- Lead Sponsor
- Canisius Wilhelmina Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Breastcancer patients who has been treated curative.
Exclusion Criteria
Severe psychopathology (for example suicidality).
Younger than 18 years old.
Breastcancerpatients treated palliative.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary outcome of the study is the level of well-being, measured by the MHC-sf<br /><br>and the level of distress, measured by the HADS.<br /><br>- Is there a significant increase in the level of well-being?<br /><br>- Is there a significant decrease in the leve of distress?</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secundary outcome of the study are the subscales from the MHC-sf.<br /><br>Is there a significant increase in the level of emotional well-being?<br /><br>Is there a significant increase in the level of psychological well-being?<br /><br>Is there a significant increase in the level of social well-being?<br /><br><br /><br>As well there wil be investigated if the level of psychological flexibility and<br /><br>engaged living will increase. When training is finished patients will be asked<br /><br>to evaluate the training.<br /><br>Is there an increasing level of psychological flexibility?<br /><br>Is there an increasing level of engaged living?<br /><br>How do patients evaluate the training?<br /><br>How do the participants evaluate the training?</p><br>