Electronic recording of patient reported outcomes in cancer patients - an mHealth Feasibility Project (PROutine)
- Conditions
- sage of a mHealth Solution for the documentation of QoLC00-D48Neoplasms
- Registration Number
- DRKS00008761
- Lead Sponsor
- Jambo9 GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
incurable cancer, regular outpatient treatment in the participating center (= 1 scheduled appointment every 6 weeks)
Exclusion Criteria
<18 years, concurrent participation in another comparable mHealth examination, limited cognition, visual-motor coordination problems or underestimation of the physician or in accordance with Mini Mental State Examination (MMSE <24) or Clock-Drawing Test (CDT> 3) (Schramm 2002), difficulties in understanding the German language in accordance with the judgment of the practitioner, significantly increased risk of death within the next three months as measured by the surprise question
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Acceptance rate and drop out rate, proportion and distribution of Missing Data. Data capture via electronic evaluation device usage and questionnaire. Over a period of up to 3 months, the data is stored on the device and then collected and evaluated centrally. Furthermore the retrospective assessment of patients and their doctors is recorded by a questionnaire.
- Secondary Outcome Measures
Name Time Method ser rating of practicality, identification of improvement opportunities. Datacapture via questionnaire after the period of use of up to 3 months.