PROMISE: Patient Reported Outcome Measures in cancer care: a hybrid effectiveness-Implementation trial to optimise Symptom control and health service Experience
- Conditions
- CancerCancer - Bowel - AnalCancer - BreastCancer - Head and neckCancer - Lung - Small cellCancer - PancreaticCancer - ProstateCancer - Oesophageal (gullet)
- Registration Number
- ACTRN12620001290987
- Lead Sponsor
- QIMR Berghofer Medical Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Active, not recruiting
- Sex
- All
- Target Recruitment
- 600
Age at least 18 years
diagnosed with invasive solid cancer
about to start or recently started treatment at one of the study sites
A tumour type or characteristic that is not appropriate for inclusion at the discretion of the Site Investigator and Coordinating PI e.g.:
oWill not return to the site for regular treatment/follow-up
oAlready using or would normally use an e-PROM tool at that site
•Treated with surgery only
•Current participation in another study that requires completion of similar PROMs
•Unable to provide informed consent
•Unable to complete the e-PROM tools remotely (e.g. a comorbid condition affecting vision, cognition or dexterity or no internet access at home)
•Unable to complete the study questionnaires in English
•Unwilling to consent to data linkage
In addition, participants who consent but do not complete the Baseline Study Questionnaire will be excluded post-consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method