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Table 1 Data collection schedule

From: Experiences of patients, family and professional caregivers with Integrated Palliative Care in Europe: protocol for an international, multicenter, prospective, mixed method study

Outcome parameter

Data collection method

Baseline

Week 1-4

Month 1

Week 5-8

Month 2

Week 9-12

Month 3

End of data collection

Patient

         

Organisation of patient’s care network, Collaboration between professional caregivers

Caregiver network analysis questionnaire

X

     

X

 

Experiences with IPC initiative, Quality of Care

Semi-structured interview

X

     

X

 
 

Diary

 

X

 

X

 

X

  

Quality of Life, Perceived symptoms

Palliative care Outcome Scale

X

 

X

 

X

 

X

 

Satisfaction with Care

Canhelp Lite

X

 

X

 

X

 

X

 

Family caregiver

         

Experiences with IPC initiative, Quality of Care

Semi-structured interview

X

     

X

 

Quality of Life, Perceived symptoms of patient

Palliative care Outcome Scale

X

 

X

 

X

 

X

 

Satisfaction with Care

Canhelp Lite

X

 

X

 

X

 

X

 

Burden & Reward of care giving

Caregiver Reaction Assessment

X

 

X

 

X

 

X

 

Professional caregiver

         

Experiences with IPC initiative, Quality of Care, Collaboration between professional caregivers

Focus group

       

X