Table 4.

Data access, exchange and consumer follow-up

Access to consumer data1	N (%)
	Health Data	Social Data
No or very limited access to consumer data	5 (11.4%)	4 (9.1%)
Limited access to consumer data	13 (29.6%)	3 (6.8%)
Moderate access to consumer data	17 (38.6%)	19 (43.2%)
Full access to consumer data	9 (20.5%)	18 (40.9%)
Care plan comprehensiveness	N (%)
No comprehensive care plan for consumers	2 (4.4%)
Care plan present but limited in scope	19 (41.3%)
Care plan for consumers - multi-component	5 (10.9%)
Care plan for consumers - extended components	20 (43.5%)
Systematic consumer follow-up	N (%)
No monitoring of care plans	0 (0.0%)
Monitoring and adjustment of care plans at least twice/year	6 (13.0%)
Tracking tests, referrals and following up	40 (87.0%)

Notes: Multi-component care plans include plans for physical health treatment, social services, participant goals and/or preferences, and plans for mental health treatment or substance use disorder treatment. Extended components category requires at least five additional components in care plan (e.g., plans for health behavior change, barriers to consumer goas, etc.).

¹Results limited to respondents who reported being directly involved in managing or delivering clinical care (N=44).