Table shows the baseline demographic, clinical and psychosocial characteristics of our patients with type 2 diabetes. There were no significant differences in any demographic, clinical, or psychosocial factors between patients followed for one year (n = 290) and those who could not be followed (n = 14). Also, even after eliminating the four deceased patients, there were no significant differences in any of the demographic, clinical, or psychosocial variables between the remaining 10 patients who were not followed for the full year and the 290 patients who were. Moreover, although six of 10 patients who dropped out were referred to local clinics because of good glycemic control, there were no significant differences in any variables between the 290 patients completing follow-up and the six referred patients. In addition, of the 32 patients who were referred to local clinics, the 6 dropouts and 26 patients who did not drop out had no significant differences in any of the variables (data not shown).
| Table 1Baseline demographic, clinical and psychosocial characteristics of patients with type 2 diabetes |
Table shows a correlation matrix of the total scores of the psychosocial inventories of the 304 patients at baseline. The DTSQ had significant, positive correlations with the W-BQ12 (correlation coefficient (r) = 0.254), SES (r = 0.128), Social Support Scale (r = 0.176), and Self-Efficacy Scale (r = 0.448) and a negative correlation with the PAID (r = -0.489). The W-BQ12 had significant positive correlations with the SES (r = 0.479), Social Support Scale (r = 0.314), and Self-Efficacy Scale (r = 0.525) and a significant negative correlation with PIAD (r = -0.555). The PAID score revealed significant negative correlations with all the other psychosocial variables, including the SES (r = -0.322), Social Support Scale (r = -0.169) and the Self-Efficacy Scale (r = -0.437). The SES showed a significant positive correlation with the Social Support Scale (r = 0.273) and the Self-Efficacy Scale (r = 0.401). A positive, significant correlation was found between the Social Support Scale and the Self-Efficacy Scale (r = 0.404).
| Table 2Correlation matrix of psychosocial variables at baseline (n = 304) |
Table displays the results of correlation coefficients by Pearson's simple correlation test and standard regression coefficients (β) by hierarchical stepwise multiple regression for the demographic, clinical and psychosocial variables and HbA1c at baseline. Baseline HbA1c was found to have significant positive correlations with, the number of diabetic complications (r = 0.168) and the baseline PAID score (r = 0.220), meaning that greater distress on diabetes was associated with a worse HbA1c value. In contrast, baseline HbA1c was found to have significant negative correlations with age (r = -0.311), diet treatment regimen (r = -0.249), and the baseline scores of the DTSQ (r = -0.219), W-BQ12 (r = -0.125), and Self-Efficacy Scales (r = -0.187), meaning that greater satisfaction, well-being and self-efficacy on diabetes were associated with a better HbA1c value. The hierarchical stepwise multiple regression model revealed that age, diet treatment regimen, and number of diabetes complications were significantly and independently associated with baseline HbA1c (Table , model 1, R2 = 0.164). In model 2 (R2 = 0.178), the DTSQ score was significantly associated with baseline HbA1c (β = -0.120, P = 0.03) after controlling for demographic, clinical, and psychosocial variables, except for PAID score. In model 3 (R2 = 0.178), the PAID score was significantly related to baseline HbA1c (β = 0.131, P = 0.017) after controlling for demographic, clinical, and psychosocial variables, except for the DTSQ score. However, no more than 17.8% of the variance in current glycemic control was accounted for by age, diet treatment regimen, number of diabetes complications, and DTSQ or PAID score.
| Table 3Simple correlation coefficients (r) and standard regression coefficients by hierarchical stepwise multiple regression (β) between baseline variables and HbA1c at baseline of patients with type 2 diabetes (n = 304). |
Table displays the results by Pearson's simple correlation test and hierarchical stepwise multiple regression for baseline demographic, clinical and psychosocial variables and one-year follow-up HbA1c. HbA1c at the one-year follow-up was found to have significant positive correlations with the baseline PAID score and to have a significant negative correlation with age, diet regimen, and the baseline scores of the DTSQ, W-BQ12, SES and Self-Efficacy Scale. A highly significant positive correlation was found between baseline HbA1c and one-year follow-up HbA1c (r = 0.675, P < 0.01). In addition, HbA1c at the one-year follow-up (7.15 ± 1.2%) had significantly better values than the baseline HbA1c (7.32 ± 1.2%) of the 290 patients (P = 0.02 by paired t-test). The hierarchical stepwise multiple regression for one-year follow-up HbA1c as a dependent variable revealed that age and diet treatment regimen were significantly and independently associated with follow-up HbA1c (Table , model 1, R2 = 0.127). In model 2 (R2 = 0.138), DTSQ score was significantly associated with follow-up HbA1c (β = -0.115, P = 0.03) after controlling for demographic, clinical, and psychosocial variables, except for PAID score. In model 3 (R2 = 0.144), PAID score was significantly related to follow-up HbA1c (β = 0.140, P = 0.014) after controlling for demographic, clinical, and psychosocial variables, except for DTSQ score. By adding baseline HbA1c to model 2, 47.9% of the variance in future glycemic control was accounted for by treatment regimen (β = -0.155, P = 0.001) and baseline HbA1c (β = 0.638, P < 0.001) in model 4. Also, by adding baseline HbA1c to model 3, 47.4% of the variance in future glycemic control was accounted for by treatment regimen (β = -0.155, P = 0.001) and baseline HbA1c (β = 0.634, P < 0.001) in model 5. The results of models 4 and 5 indicate that better current HbA1c and diet treatment are significant predictors of better future HbA1c. The statistically significant contribution of the DTSQ and the PAID to future HbA1c disappeared after adjustment for baseline HbA1c.
| Table 4Simple correlation coefficients (r) and standard regression coefficients by hierarchical stepwise multiple regression (β) between baseline variables and HbA1c at 1 year follow-up of patients with type 2 diabetes (n = 290). |
Concerning treatment regimen, medication details (n = 231) are as follows: 74% of the patients on medication were treated with OHA (n = 171) and 26% were treated with insulin alone or insulin plus OHA (n = 60). After the one-year follow-up, the change of HbA1c in patients who were treated with diet only was from 6.71 ± 1.1% to 6.42 ± 0.82% (P = 0.022), the change in patients who were treated with OHA was from 7.32 ± 1.0% to 7.23 ± 1.1% (P = 0.265), and the change in patients who were treated with insulin or insulin plus OHA was from 7.93 ± 1.4% to 7.60 ± 1.4% (P = 0.012).