An online lifestyle intervention to improve cognition of cancer patients
- Conditions
- cancer-related cognitive impairmentchemobrain10009841
- Registration Number
- NL-OMON50422
- Lead Sponsor
- Vrije Universiteit Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 230
* Having received chemotherapy treatment for any recently diagnosed non-CNS
cancer
* Chemotherapy treatment has been completed
* Presence of cognitive complaints
* ><= 18 years of age
* Written informed consent
* Primary or secondary brain tumours
* Insufficient mastery of the Dutch language
* History of brain injury with loss of consciousness
* History of brain surgery
* Currently under active treatment for psychiatric disorders
* Neurodegenerative disorders
* Self-reported substance abuse
* Severe visual impairments
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Feasibility study:<br /><br>Compliance rate of the participants after 3 months, if there is a compliance of<br /><br>more than 50% after 3 months and the feedback from the structured interview is<br /><br>mostly positive we will continue with the main study.<br /><br><br /><br>Main study:<br /><br>The change in subjective cognitive functioning between baseline and 6 months<br /><br>later, comparing the effect of MFB to no intervention. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Feasibility study:<br /><br>Usability<br /><br>Areas of improvement<br /><br><br /><br>Main study:<br /><br>The change in objective cognitive functioning between baseline and 6 months.<br /><br>The change in lifestyle functions between baseline and 6 months.<br /><br>The influence of other parameters such as level of education, work performance,<br /><br>self-efficacy, type of cancer, type of treatment, age, gender, psychological<br /><br>functioning on the effect of the intervention. </p><br>