The Nausea Care App in patients receiving chemotherapy: A Randomized Controlled Trial
Withdrawn
- Conditions
- Patienten die chemotherapie krijgen voor mamma-, ovarium-, hodgkin-, non-hodgkinNauseavomiting
- Registration Number
- NL-OMON43482
- Lead Sponsor
- Oncologie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Withdrawn
- Sex
- Not specified
- Target Recruitment
- 206
Inclusion Criteria
- Adulta (18+)
- Diagnosed with oncologic disease
- Precription with AC, TAC, R-CHOP, ABVD, Taxol/Carboplatin
- Able to read and speake Dutch
- Own a smartphone (Iphone, Android)
- Capable to give written informed consent
Exclusion Criteria
- Patient who received chemotherapy prior to study participation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main study parameter include differences between NCAG and CG, regarding:<br /><br>Chemotherapy induced nausea measured as a patient reported visual analoge scale<br /><br>(VAS) and defined as a VAS equal or above 5 mm.</p><br>
- Secondary Outcome Measures
Name Time Method <p>- Number of days including occurence of nausea.<br /><br>- Number of days including occurrence of vomiting<br /><br>- Number of days including usage of escape medication<br /><br>- QoL-scores<br /><br><br /><br>Numbers and percentages of NCAG who:<br /><br>- find the NCA easy to download<br /><br>- find the instructions clearly described<br /><br>- received information as requested<br /><br>- find the NCA useful as a reminder for taking anti-emetics<br /><br>- would recommend the NCA to other patients<br /><br><br /><br>Contacting the ward by NCAG and CG:<br /><br>- number of days including extra visits<br /><br>- number of days including extra phone calls</p><br>