Basic Information
                                                
                          
                             
                              Abbreviated name 
                                                          
                             
                              QUALITY OF END-OF-LIFE CARE (QEOLC-10): COMMON SOLUTION, PATIENT VERSION                            
                           
                                                    
                          
                                                      
                               
                                Items 
                                                                
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                                  The number of questions in the survey                                                                  
                                
                                                               
                               
                                10                              
                             
                                                        
                               
                                Short description 
                                                              
                               
                                The common solution questionnaire provided here is composed of 10 items and may be used with patients who have been asked to evaluate the quality of end-of-life care.  The 10 items were selected from a larger set of items using factor analytic approaches, and represent all five domains that we had identified previously as important to the quality end-of-life care.  The items are the same for all respondent-types, making it easier to compare scores across respondents. The items provide a single score, derived as a simple mean of item values.                              
                             
                                                      
                          
                             
                              PCCC or QoL? 
                                                            
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                                This compendium contains patient-reported measures that are either designed to specifically measure aspects of Person Centred Co-Ordinated Care (P3C), or alternatively tools that are designed to measure some aspect of Quality of Life (QoL) or Health Related Quality of Life (hrQoL).  All the measures in this compendium have been broadly categorised into one of those two concepts.                                                               
                              
                                                           
                             
                              Person Centred Coordinated Care                             
                           
                                                      
                               
                                Main Domains Measured 
                                                                
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                                  This is the key domains that the measure is targeting.                                                                   
                                
                                                               
                               
                                Communication skills, symptom skills, affective skills, patient-centered values, and patient-centered systems                              
                             
                                                      
                          
                             
                              Type of measure 
                                                            
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                                The measures in this compendium can take a variety of forms. Generally, they will be either Patient Reported Outcome Measure (PROM) or Patient Reported Experience Measure (PREM).  However, we have also included a few measures that are completed by proxy-individual (PROXY), which are useful in instances where the respondent cannot answer directly (e.g. dementia or end of life). Sometimes, these measures can even be a composite of these types, and target both experiences and outcomes – we have labelled these measures “PROEMs”.                                                              
                              
                                                           
                             
                              Patient Reported Experience Measure                            
                           
                                                      
                               
                                Respondent 
                                                                
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                                  The person that fills in the questionnaire - e.g. patient, Health Care Professional, or proxy (normally a carer or family member)                                                                  
                                
                                                               
                               
                                Patients                               
                             
                                                        
                               
                                Licence link 
                                                                
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                                  A link to the vendor/supplier for licensing of the measure