Table 1.

Measures of COPILOT-study

	Concept	Instrument	0*	12	24
Patient
Primary outcomes	patients’ experience of health care delivery (1)	PACIC	X	X	X
	patients’ experience of health care delivery (1)	NPS	X	X	X
	patients’ experience with integration of care (1)	QUOTE	X	X	X
	Quality of life, generic health (2)	EQ-5D-5L	X	X	X
	Quality of life, social perspective (2)	ASCOT	X	X	X
	Impact of self-reported disease-related limitations (2)	Developed questions	X	X	X
	Clinical indicators of disease severity and activity (2)	GPs electronic patient records	X		X
	Resource use & sickness leave (4)	Tic-P	X	X	X
Other variables	Age		X	X	X
	Gender		X	X	X
	Social economic status		X	X	X
	n chronic diseases		X	X	X
	Type chronic diseases		X	X	X
	Health literacy	HLS-EU-Q16	X	X	X
	Functional and social ability	InterRAI CU-SR	X	X	X
Primary care professional
Primary outcomes	Job satisfaction (3)	Developed questionnaire	X		X

PACIC = patient assessment of chronic illness care; NPS = net promotor score; QUOTE = quality of care through patients’ eyes; EQ-5D-5L = EuroQol 5D – 5 level version; ASCOT = adult social care outcomes toolkit; CU-SR = check-up self-report; Tic-P = trimbos and iMT questionnaire on costs associated with psychiatric illness; HLS-EU-Q16 = 16-item Dutch version of the European health literacy short survey questionnaire; VAS = visual analogue scale.

^*Months after baseline.

(1) Patient experience with chronic primary care.

(2) Patients’ health.

(3) Societal costs and costs of resources use.

(4) Care professionals’ experiences with management of multimorbidity.