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. Author manuscript; available in PMC: 2011 Feb 23.
Published in final edited form as: Psychosomatics. 2011 Jan–Feb;52(1):1–18. doi: 10.1016/j.psym.2010.11.007

Table 2.

Psychosocial interventions

Reference Study Design Depression Entry Criteria M(SD) Baseline HbA1c levels Enrolled/Completed Treatment modality/Duration/Type Depression Measures Significant Depression Outcomes Significant Health/Glucose Outcomes Methodological Characteristics
Lustman et al., 1998 RCT of CBT w/education, education only DIS diagnosis of MDD, BDI>13 10.2 (3.6)% for patients in the intervention group, 10.4 (3.1)% in the control group 51/42 CBT, 10 weeks, individual BDI ITT: 70.8% CBT achieved remission (BDI<9) v. 22.2% education (p<.001) and 66.6% CBT achieved clinical improvement v. 29.6% education (p=.01). At 6-mo f/u, 58.3% CBT in remission v. 25.9% education (p=.03) and 58.3% CBT achieved clinical improvement v. 29.6% education (p=.01). No difference in HbA1c levels at post-treatment. At 6-mo f/u, CBT = 9.5% and education-only = 10.9% (p=.03) RCT w/education-only comparison & 6-month follow-up interval, ITT analyses, age 21-70, type 2 only, MDD criterion, HbA1c as primary outcome measure
Lamers et al., 2006 RCT of MPI, TAU MINI diagnosis of Major or Minor Depression, HDRS > 18 TBA Goal of 180 CBT, up to 10 visits over 3 mos., individual at-home nurse-delivered BDI TBA N/A RCT w/ TAU comparison and 9 month follow-up interval, planned ITT analyses, age 60 and over, type 2, Major and Minor Depressive Disorder, HbA1c not an outcome
Van Bastelaar et al., 2008 RCT of web-based CBT, wait-list control CES-D > 16 TBA Goal of 286 CBT, 8 weeks, web-based CES-D TBA TBA RCT design w/waitlist control and 6 month follow-up, planned ITT analyses, age 18 or over, type 1 or 2, elevated depressive symptoms, HbA1c a secondary outcome measure
Simson et al., 2008 RCT of supportive psychotherapy, TAU HADS > 7 8.1 (1.9)% 30/30 Hospitalized for diabetic foot syndrome Supportive psychotherapy, weekly (avg. 5) sessions, individual HADS HADS depression change SP: -1.6 TAU: 0.3, p=.02 HADS anxiety change SP: -0.5 TAU: 1.6, p=.02 PAID change SP: -5.5 TAU: 2.1, p=.008 N/A RCT design w/TAU comparison and limited follow-up, pre-post completer analyses, age <= 75 years, type 1 or 2, elevated depressive symptoms, HbA1c not an outcome measure
Georgiades et al., 2007 Open-label of group CBT BDI>=10 7.6 (1.6)% 90/65 CBT, 16 sessions over 14 weeks for 90 minutes, group BDI, HDRS BDI decreased significantly from baseline to 12-month follow-up (p<.001). HDRS decreased significantly from baseline to 3-month follow-up (p<.001) No significant change on HbA1c. Within subjects changes on BDI had no significant effect on HbA1c Single-group open-label quasi-experimental design with 12-month follow-up, pre-post completer analyses, 18 and over, type 1 and 2, depressive symptoms, HbA1c outcome measure
Rossello & Himenez-Chafey, 2006 Open-label pilot study of group CBT Depressive symptoms on CDI 9.3% (1.9)% 16/11 CBT, 12 weeks for 2 hours, group CDI Pre CDI=19.4 and post CDI=9.9, p<.05. No difference in glycemic control or diabetes self-care N/A Open-label pilot without randomization, control group or follow-up, pre-post completer analyses, age 13-17, type 1, elevated depressive symptoms, HbA1c outcome measure