Cancer, specifically a brain tumor or lung cancer
Conditions
Interventions
Medical specialists and nurse specialists who are likely to have consultations with study patients, whether in the intervention or control group, during the three months of research, receive a 1-hour
Sponsors
Your Years B.V.
Eligibility
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study a participant must meet all of the following criteria: 1) Advanced (grade III/IV) brain tumor or lung cancer; 2) Age 18 years or older; 3) Own an iPhone 5s or newer; 4) Have at least one clinical oncology appointment within the three months of the research; 5) Fluent in Dutch.
Exclusion criteria
Exclusion criteria: 1) Being a participant in another clinical study (to avoid potential contamination of the findings in the other study); 2) Unable physically and/or mentally to use the app on a daily basis and/or participate in an interview and/or fill out a digital questionnaire.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint is whether or not documentation of (changes in) patient personal goals is present in case of documented medical decision-making in the medical file. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoints are dialogue on patient personal goals in outpatient consultations and patient experienced level of goal concordant decision-making. Other endpoints include potential spill over of the briefing, quality of life, depression and anxiety, emergency visits and hospitalisations, likeliness to recommend Goings-On, frequency of use of Goings-On, consultation time and patients and clinicians thoughts in getting goal-concordant care . | — |
Contacts
Public ContactPetra Hoogendoorn
LUMC
Outcome results
None listed