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. 2018 May 26;178(7):930–940. doi: 10.1001/jamainternmed.2018.2317

Table 3. Effect of the Intervention on Patients’ Symptoms of Depression and Anxietya.

Outcome Patients/Clinicians, No.b Mean Value for Psychological Symptoms (95% CI) at Follow-upc β (95% CI)d P Value
Control Intervention
Depression Symptoms
3 Months after target visit
2-Indicator latent variablee,f 262/113 0.20 (−0.02 to 0.42) 0.26 (−0.04 to 0.55) −0.10 (−0.33 to 0.12) .37
Standard PHQ-8 composite scoreg,h 359/119 4.88 (4.23 to 5.54) 5.92 (5.19 to 6.66) 0.26 (−0.57 to 1.10) .54
6 Months after target visit
2-Indicator latent variablee,i 262/113 0.24 (0.07 to 0.42) 0.40 (0.11 to 0.69) 0.21 (−0.04 to 0.46) .11
Standard PHQ-8 Composite Scoreg,j 314/118 4.84 (4.17 to 5.51) 5.927 (5.05 to 6.81) 0.45 (−0.48 to 1.37) .34
Anxiety Symptoms
3 Months after target visit
2-Indicator latent variablee,h 277/119 0.22 (0.01 to 0.43) 0.28 (−0.04 to 0.60) −0.03 (−0.23 to 0.16) .73
Standard GAD-7 composite scoreh,k 366/122 3.00 (2.44 to 3.57) 3.26 (2.64 to 3.89) 0.04 (−0.95 to 1.03) .94
6 Months after target visit
2-Indicator latent variablee,h 277/119 0.21 (−0.05 to 0.47) 0.30 (0.00 to 0.59) −0.04 (−0.25 to 0.16) .69
Standard GAD-7 composite scoreh,k 327/119 3.08 (2.44 to 3.72) 3.375 (2.67 to 4.08) −0.11 (−1.20 to 1.00) .85

Abbreviations: CFA, confirmatory factor analysis; GAD-7, 7-item Generalized Anxiety Disorder survey; PHQ-8, 8-item Patient Health Questionnaire; WLSMV, weighted least squares with mean and variance adjustment.

a

The coefficient estimates and P values were based on complex single-group regression models with patients clustered by treating clinician, with intervention group as the predictor of interest, and with adjustment for any variables that confounded the association between the intervention-group predictor and outcome. A variable was identified as a confounder if its addition to the bivariate model changed the coefficient for the intervention group by 10% or more in either direction. For the latent variable outcomes, the sample included only those patients who provided data for both indicators at all 3 time points (baseline, 3-month follow-up, and 6-month follow-up). For all outcomes, patients were included only if they provided data for the outcome and any covariates in the model.

b

Number of patients/number of clinician clusters.

c

For the standard composite scores, the unadjusted mean for the standard composite score, computed with data from the follow-up questionnaire. For the 2-indicator constructs, the mean value of the construct on the follow-up questionnaire, based on a 2-group CFA model using patients with complete data for the 3 time periods, with scalar measurement invariance imposed between groups and over time, and with the baseline mean for the control group fixed at 0.

d

Point estimate and confidence interval for the regression coefficient from a single-group model with the outcome regressed on the intervention-group predictor, after adjustment for any confounders.

e

Probit regression model, estimated with WLSMV.

f

Adjusted for baseline level on the outcome and the patient’s racial/ethnic minority status.

g

Robust linear regression model, estimated with restricted maximum likelihood.

h

Adjusted for baseline level on the outcome.

i

Adjusted for patient’s baseline level on the outcome, age, racial/ethnic minority status, education, and self-identified health status; and for clinician type and specialty.

j

Adjusted for patient’s baseline level on the outcome and clinician specialty.

k

The outcome was defined as censored from below; Tobit regression model estimated with WLSMV.