Efficacy and Safety of a Decision Support Intervention for Basal Insulin Self-Titration Assisted by the Nurse in Outpatients with T2DM: A Randomized Controlled Trial.

OBJECTIVE: The main aim of this study was to evaluate a combined fasting blood glucose based dosage self-titration setting and decision supported telephone coaching intervention on glycemic control and diabetes self-management skills, compared to the conventional care.
METHODS: A 12-week, single-blinded, randomized controlled trial was conducted on adults with type 2 diabetes (T2DM) primarily treated with basal insulin. After randomization, the intervention group (IG, n = 426) received a basal insulin self-titration decision support intervention administered by the Diabetes Specialty Nurses while the control group (CG, n = 423) received conventional care for 12 weeks, both included five telephone interviews. The primary efficacy endpoint was the effect of intervention on glycemic control, measured as the change in glycated hemoglobin (HbA1c) from baseline to Week 12 (after intervention) compared to the control group. Other endpoints included comparisons of the effects of intervention on fasting plasma glucose (FPG), postprandial plasma glucose (PPG), body weight, Michigan diabetes knowledge test (MDKT), diabetes empowerment scale-short Form (DES-DSF), and summary of diabetes self-care activities (SDSCA). Changes in the primary and secondary outcomes were compared using the t-test for continuous variables with a normal distribution and χ 2-test for categorical variables.
RESULTS: The IG showed more improvements on mean HbA1c, compared to the CG (-2.8% vs -1.8%), so did the FPG, PPG, MDKT, DES-DSF and SDSCA (all P<0.01) after the 12-week follow up. Though the final mean insulin dose in the IG was higher than the CG at the end of the study (0.32 U/kg vs 0.28 U/kg), the changes of body weight were similar between the two groups (0.46kg vs 0.40kg, P=0.246), and the proportion of patients with hypoglycemia events during the whole trial were similar (20.65% vs 17.73%, P=0.279).
CONCLUSION: Decision supporting of basal insulin glargine self-titration assisted by Diabetes Specialty Nurses is effective and safe in patients with T2DM. Decision supported telephone coaching intervention offers ongoing encouragement, guidance, and determination of relevant sources of decisional conflict, facilitating adjusting the insulin dose.

Introduction

T2DM has become a major public health challenge in China, because its prevalence has increased from 3.2% in 1996 to 12.8% in 2017.1 However, according to the national analysis, only 32.2% patients with T2DM have received appropriate treatment, and the percent of adequate glycemic control is only about 37.6% for patients on insulin therapy, much lower than the patients (50.2%) on oral antidiabetic drugs (OADs).2

For patients with T2DM who have suboptimal glycemic control and show no response to OADs, basal insulin (BI) is one of the first-choice for glucose treatment.3,4 Numerous randomized controlled trials (RCTs) and real-life studies,4 including data from our country,5,6 have validated the efficacy of BI on glycemic control, now the decade of second-generation basal insulin analogues has come.7 U-100 glargine, the first long-acting insulin analog approved in China, reduces the risk of symptomatic and nocturnal hypoglycemia to a greater extent than NPH insulin in real-life studies from our country.6,8 Glargine has been widely used in China for treatment of T2DM, with cost-saving advantage9 and acceptable side-effects, such as slight weight gain and low hypoglycemia risk.9,10 However, several critical barriers to BI therapy pose a challenge, including suboptimal dose titration and fear of hypoglycemia.

Timely insulin initiation and adequate titration of the insulin dose by either physicians or patients are essential steps to achieve and maintain treatment goals. In a real-world study for T2DM, 43.4% patients’ dose was barely adjusted 6 months after initiation of BI in our country,6 in another study the proportion of insulin discontinuation was high within 6 months after initiating BI.11 The situation of delayed insulin initiation and suboptimal dose titration in Chinese patients with T2DM is usual,6 which could be attributed to limited healthcare resources and clinical inertia among both patients and clinicians. The “clinical inertia” in USA also results in poor glycemic control, it was reported while >75% of healthcare professionals discussed titration at the initiation visit, only 16% to 28% of patients remembered such discussions, many (32–42%) were unaware of the need to titrate BI.12 In our country, most of the patients not usually see their doctors and nurses after initiation of basal insulin, we even saw a patient full of complain of insulin injection after keeping using 0.5 U/day insulin for several weeks. BI discontinuation significantly associated with hospital level, patient recruitment setting, age, education level, out-of-pocket ratio, et al.11 A disconnect exists between doctors and patients perceived barriers to effective BI titration, only patient-led initiation and titration of basal insulin without help from the nurse seemed not enough for glucose control in our country,13 so we want to find more effective and practical support tools to assist patients for BI titration.

Patient empowerment promotes self-care and development of innate capacity of responsibility through education and motivation by healthcare professionals.14 Health-related decision aids improves knowledge of treatment options, provides realistic expectations of the benefits and risks, and allows choices consistent with values.15 Dose titration of glargine based on fasting blood glucose levels using an algorithm is reported as a safe and effective strategy.16 Nurse-administered telephone intervention is a well-recognized approach to improve glycemic control with insulin titration.17,18 The purpose of this research was to evaluate the impacts of an fasting blood glucose based dosage titration setting and decision supported telephone coaching intervention by nurses on outpatients with T2DM.

Methods

Study Design and Setting

This 12-week, single-blinded, randomized controlled trial was conducted in our department with an intervention group (IG) and a control group (CG). The study protocol was approved by the Ethics Committee of the Third Affiliated Hospital of Sun Yat-sen University. All patients provided written informed consent prior to the participation in the study. After the last interview, the patients in the control group were offered the same education and tools as those in the intervention arm. The study was conducted from January 2017 to July 2018.

Participants and Randomization

Participants were recruited from the Third Affiliated Hospital of Sun Yat-sen University in China. Both the outpatients and the inpatients were screened. Besides face to face, the patients were invited by telephone to participate into the study and received an offer to meet the investigator. After confirming their intent to participate, patients signed an informed consent form and received the baseline interview.

Inclusion criteria were as follows: 18 ≤ age ≤ 70 years, with a diabetes duration of ≥ 2 years, having used two to three oral antidiabetic drugs (OADs) before screening, 7 < HbA1c <11%, and 20 ≤body mass index (BMI) < 30 kg/m2. Moreover, all patients must agree to perform blood glucose monitoring using a blood glucose meter and completed our follow-up survey and questionnaires. Exclusion criteria were as follows: current or previous use of insulin, acute or severe chronic diabetic complications or illnesses, and positive for glutamic acid decarboxylase antibodies. About four to five patients were enrolled in a day.

After enrollment, all patients were given baseline interview with the responsible doctor and nurse. At baseline, demographic and anthropometric data were recorded. FPG, PPG, and HbA1c were measured. The scores of MDKT, DES-DSF, and SDSCA were evaluated by the nurses. And then they were provided with standard diabetes education by the nurses, regard to diet, exercise, glucose monitoring, insulin injection, and hypoglycemia. They were given basal insulin glargine treatment by the doctor, beginning with 0.25U/kg per day. All patients received standard injection guidelines including rotation habits, spacing injections 1 cm apart, and using a new needle with every injection. After that, a computer-generated simple randomization table assigned patients at a 1:1 ratio to either the intervention or conventional care (control group) arms, the previous OADs (including sulphonylureas/glinides) were continued. The time spent between the enrollment and randomization was 1–2weeks.

Patients were urged to perform glucose monitoring fasting glucose per day and random glucose when they had hypoglycemic symptoms for the duration of the study. Minor hypoglycemia was defined as symptoms confirmed by a blood glucose concentration < 3.9 mM, with prompt recovery after self-administered carbohydrate. Major hypoglycemia was defined as an event requiring the assistance of another person to administer carbohydrate, glucagon, or other resuscitative treatments. The patients were asked to record their insulin dose, hypoglycemic events and other adverse effects (AE) during the study. And they should adjust insulin doses by the doctors’ suggestions as the needed, they could see the doctors as usual outpatients when they needed. Glycemic targets were given by the responsible doctor for each patient. All baseline assessments were repeated at the end of the study (Week 12). Patients from both arms were required to bring their blood glucose meters to clinic at the end of the study. Table 1 shows the similarity and differences in care between the two groups.

Table 1

The Similarity and Difference Between the Intervention Group and Control Group

The Care in Our Study	Intervention Group (n=436)	Control Group (n=433)
Screening and sign informed consent form	Yes	Yes
Baseline(before randomization)	Yes	Yes
— Collect demographic and anthropometric data
— Test HbA1c, FPG, and 2hPPG
— Evaluate the score of MDKT, DES-DSF, and SDSCA
— Standard diabetes education (including insulin injection)
— Begin basal insulin glargine treatment
Randomization	Yes	Yes
Adjust insulin doses by the doctors’ suggestions	Yes	Yes
Monitoring fasting glucose per day and random glucose	Yes	Yes
Record insulin dose, hypoglycemic events, and other AE	Yes	Yes
Five coaching calls at the 1, 2, 4, 8, 12 weeks by the nurse
— Collect the insulin dose and the AE of the participants	Yes	Yes
— Guide the Insulin dose titration	Yes	No
Contact the investigator for emergency problems	Yes	Yes
End of the study (12 weeks after randomization)	Yes	Yes
— Collect demographic and anthropometric data
— Test HbA1c, FPG, and 2hPPG
— Evaluate the score of MDKT, DES-DSF, and SDSCA
— Recycle the diary (including the insulin dose, hypoglycemic events and other AE)

Abbreviations: FPG, fasting plasma glucose; PPG, postprandial plasma glucose; MDKT, Michigan diabetes knowledge test; DES-DSF, diabetes empowerment scale-short Form; SDSCA, summary of diabetes self-care activities; AE, adverse events.

Nurses

The Diabetes Specialty Nurses were chosed to finish the study. They must receive standardized training with regard to using decision supported system, empowerment model, procedures for intervention before the study. The training was provided through group discussion, role play and lectures. Only qualified nurses were involved in providing the decision support for this study.

A study day was held for participant nurses to review the protocol, randomization schedules, and Clinical Report Forms (CRF), and to be trained in case record, diabetic education, self-dose-adjustment intervention, and follow-up (including evaluating the scores of MDKT, DES-DSF, and SDSCA) of the patients.

Intervention Group

The patients in this group received the basal insulin self-titration decision support program. Intervention participants received one baseline in-person dosage setting and decision coaching session to empower adjustment followed by 5 coaching calls at the 1, 2, 4, 8, 12 weeks delivered by the same nurse. Participants were guided towards personalized dosage decisions according to their individual risk factors in every call. A fasting blood glucose based dosage titration protocol was developed to assist with clarifying values for decision options (shown in Table 2).

Table 2

Fasting Blood Glucose Based Dosage Titration Protocol

Fasting Capillary Glucose (mmol/L)	Glargine Dose Adjustment (U)a
≤2.8	−6 (if total dose > 45 U, reduce 15%), contact the investigator as a emergency problems
2.9–3.8	−4 (if total dose > 45 U, reduce 10%)
3.9–4.3	−2 (if total dose > 45 U, reduce 5%)
4.4–6.1	0
6.2–7.8	+2
7.9–9.9	+4
≥10	+6

Notes: aDose should be adjusted every 3–4 days to achieve a target range for fasting capillary glucose of 4.4–6.1mmol/L. Change in insulin dose were based on the median of fasting capillary glucose values measured on 3 consecutive days of which the last is the day when titration is to occur.

Telephone follow-up sessions in the five key weeks were conducted by diabetes specialist nurses selected to complete the study. During the coaching calls, titration decisions to achieve personal glycemic targets were discussed and new or modified dosage regimens were recommended, depending on individual circumstances. The optimal insulin glargine dose was defined as that at which patients achieved at least fasting blood glucose values within the predetermined glycemic target. In cases whose glycemic target was not achieved, problem solving for minimizing barriers to goal attainment was implemented, supported by decision coaching for working through relevant decisional conflicts. Detailed notes were written following each coaching call to record blood glucose, insulin dose, dosage titration, and adverse events (including hypoglycemia). In addition to the telephone visits, the patient could contact the investigator for emergency problems.

Control Group

The patients in this group only adjust their insulin doses based on the doctors’ suggestions as needed (seen in Table 2). During the 12-week follow-up, the participants were also followed by 5 coaching calls at the 1, 2, 4, 8, 12 weeks delivered by the same nurse. But the nurses only collected the insulin dose and the adverse effects of the participants, without any suggestions for their insulin dose titration. Detailed notes were also written following each coaching call to record blood glucose, insulin dose, dosage titration, and adverse events (including hypoglycemia). The patient could also contact the investigator for emergency problems.

Study Endpoints

The primary efficacy endpoint was the effect of intervention on glycemic control, measured as the change in HbA1cfrom baseline to Week 12 (after intervention) compared to the control group. Other endpoints included comparisons of the effects of intervention on FPG, PPG, body weight, Michigan diabetes knowledge test (MDKT), diabetes empowerment scale-short Form (DES-DSF), and summary of diabetes self-care activities (SDSCA). Tests were translated into Chinese using the academic translation procedure. Outcomes were assessed at baseline and the end of the study (after 12-week follow-up). Safety (including hypoglycemia events) during the study were also assessed.

Instruments and Measures

Participants completed a questionnaire electronically or on paper at the outpatient clinic before randomization, and at the end of the intervention. It included items on demographics, disease duration and treatment, and 3 validated scales or scores.

The 23-item Michigan Diabetes Knowledge Test (MDKT) assesses diabetes-related knowledge of patients. The MDKT included 23 items divided into two subscales: the general diabetes subscale with 14 items (items 1–14) (e.g. “Which should not be used to treat low blood glucose?”) and the insulin-use subscale with 9 items (items 15–23) (e.g. “If you are sick with the flu, which of the following changes should you make?”). Each item has three or four answer categories, one of which is correct. Higher scores indicated better the knowledge level of the patients. Cronbach’s coefficient for general and insulin-use subscales respectively was 0.71 and 0.75.19 The Cronbach’s coefficient of the Chinese version of MDKT was 0.77.20

The 5-item Diabetes Empowerment Scale-Short Form (DES-DSF) assesses individual beliefs regarding management of the psychosocial aspects of diabetes using five response options (1 = “never” to 5 = “always”). The resulting score multiplied by four to obtain standard score (range:20–100points), higher scores indicate better individual beliefs. DES-DSF was one of the questionnaires of the Second Diabetes Attitudes, Wishes and Needs (DAWN2). The questionnaire was translated into the primary local language(s) in 17 countries (USA, Canada, UK, China, etc), then back translated and a harmonization process undertaken to ensure consistency with the original questionnaire, the Cronbach’s alpha coefficient of China was 0.68.21

The 13-item Summary of Diabetes Self-care Activities Measure (SDSCA) evaluates diabetes self-management by examining six aspects of the regimen (diet, exercise, medication taking, blood glucose testing, foot care, and smoking). Respondents recorded the degree of frequency of performance of various activities over the previous 7 days. Scores for each dimension are calculated as the averages of scores on individual items and range between 0 and 7, higher scores indicate higher scores indicate better diabetes self-management. Average inter-item correlations within scales were high (mean = 0.47) and test-retest correlations were moderate (mean = 0.40).22 The Cronbach’s coefficient of the Chinese version of SDSCA was 0.62 to 0.92, and internal consistency was1.00.23

Statistical Analysis

The study sample size was calculated using a formula to test the difference between two independent sample proportions. We powered our study based on the primary outcome, glucose control (HbA1c), after adding insulin glargine to OADs for 12 weeks. According to the RCT which compared patient-led and physician-led insulin titration, to observe a minimal clinically difference in HbA1c change of 0.17% from China,13 two-sided α=0.05 and 1-β=0.90, allowing for an attrition rate of 20% from baseline to follow-up, we will need to recruit 112 participants in the intervention group and 112 in the control group, across the study. Baseline characteristics will be summarised using mean and SD for continuous variables, and n (%) for categorical variables. Baseline characteristics between the two groups will be compared using either the t-test (continuous data) or χ2 test/Fisher’s exact test (categorical data). Multivariate linear regression was used to assess whether the intervention affected glycemic outcomes, MDKT, DES-DSF, and SDSCA scores while controlling the following potential confounding factors: age, gender, educational level, BMI, fasting C-peptide, numbers and types of OADs, complication, and comorbidities. Changes in the outcomes were compared using the t-test for continuous variables with a normal distribution and χ2-test for categorical variables. The significance level was set at 0.05. All statistical analyses were performed using IBM SPSS, version 25. Significance was defined as two-tailed P < 0.05.

Results

Participant Characteristics

Overall, 894 participants were enrolled into the study. 869 patients were randomly assigned into two groups: 434 patients in the intervention group and 435 patients in the control group. The reason for screening failures of the 25 patients was HbA1c values outside the prespecified interval for inclusion (after central laboratory report) or they refused to sign the informed consent form. Finally 849 patients (97.7%) completed the trial. Three patients in the IG and five patients in the CG discontinued the study due to consent withdrawal, three patients in the IG and four patients in the CG were lost to follow-up, while two patients in the IG and three patients in the CG discontinued for other reasons. A similar proportion of participants in both groups completed the study; 426 (98.2%) in the IG and and 423 (97.2%) in the CG, respectively (detailed data are shown in Figure 1). Demographic and baseline characteristics of patients were not markedly different between the two groups (Table 3). According to patient reported medical history, the most frequent underlying diabetes related comorbidities were: hypertension (15.9% vs 17.5% in the IG and CG) and coronary artery disease (6.2% vs 5.0% in the IG and CG). The previous OADs of the ITT population at baseline are shown in Table 3. Metformin treatment was present (alone or in combination with other agents) in 86.9% and 83.9% of patients in the IG and CG. In the IG and CG, the percents in use of α-glucosidase inhibitors were 84.3% and 82.8%, sulfonylureas were 58.8% and 61.1%, DPP-IV inhibitors were 19.1% and 21.6%, glinides were12.9% and 11.5%, SGLT2 inhibitors were 7.6% and 9.4%, respectively. The diabetes related complications in the IG and CG are as follows: 27.9% and 26.4% for peripheral angiopathy, 17.7% and 19.0% for peripheral neuropathy, 13.1% and 12.0% for diabetic nephropathy, 7.4% and 8.3% for diabetic retinopathy, respectively. Fasting C-peptide levels are also reported in Table 3.

Figure 1

Trial profile.

Table 3

Demographic and Clinical Characteristics at Baseline

Characteristics	Intervention Group (n=434)	Control Group (n=435)	P-valuea
Gender
Male/Female	263(60.6%)/171(39.4%)	248(57%)/187(43%)	0.283
Age (years)	53.62±14.33	54.77±13.43	0.224
Duration (years)	6.39±5.54	7.88±6.13	0.139
Education level (n)
Middle school or lower	205(47.2%)	184(42.3%)	0.255
High school	133(30.6%)	137(31.5%)
College	96(22.1%)	114(26.2%)
BMI (kg/m2)	23.51±2.25	23.79±2.72	0.100
Fasting C-peptide (nmol/L)	0.37±0.23	0.35±0.21	0.114
Numbers of OADs
2	90 (20.7%)	111 (25.5%)	0.159
3	330 (76.0%)	324 (74.5%)
Type of OADs
Metformin	377 (86.9%)	365 (83.9%)	0.217
α-Glucosidase inhibitors	366 (84.3%)	360 (82.8%)	0.532
Sulfonylureas	255 (58.8%)	266 (61.1%)	0.446
DPP-4 inhibitors	83 (19.1%)	94 (21.6%)	0.363
Glinides	56 (12.9%)	50 (11.5%)	0.526
SGLT2 inhibitors	33 (7.6%)	41 (9.4%)	0.336
Comorbidity status
Hypertension	69 (15.9%)	76 (17.5%)	0.534
Coronary artery disease	27 (6.2%)	22 (5.0%)	0.457
Diabetic complication
Peripheral angiopathy	121 (27.9%)	115 (26.4%)	0.632
Peripheral neuropathy	77 (17.7%)	83 (19.0%)	0.611
Diabetic nephropathy	57 (13.1%)	52 (12.0%)	0.600
Diabetic retinopathy	32 (7.4%)	36 (8.3%)	0.620

Notes: Data are expressed as the N(%), or mean ± SD. P-valuesa are for comparisons between the two groups.

Abbreviations: OADs, oral antidiabetic drugs; DPP-4, dipeptidyl peptidase-4; SGLT2, sodium-glucose cotransporter 2.

Glycemic Control

HbA1c, FPG, and 2hPPG at baseline and end of the intervention are presented in Table 4. We observed a significant decrease in HbA1c levels in both groups. After 12 weeks of glargine treatment, mean HbA1c reduction in our patient population was −2.3 ± 2.6%. Mean changes in HbA1c in the intervention group were better than the control group (−2.8 ± 1.3% vs −1.8 ± 1.1%, P<0.001). The intervention group showed greater reduction of FPG (−2.63 ± 1.24mmol/L vs1.67 ± 1.39mmol/L, P<0.001) and 2hPPG (–3.02 ± 2.31 vs 2.34 ± 2.03mmol/L, P<0.001) than the control group (seen in Table 4, both P<0.001). We have stratified the post-intervention results in terms of age, sex, educational, diabetic complication, and comorbidity status in Table 5.

Table 4

Glycemic Control

Parameter	Intervention Group (n=426)	Control Group (n=423)	aP value
HbA1c (%)
Baseline	9.42 ± 1.99	9.23 ± 1.75	0.146
Post-intervention	6.6 6± 1.31	7.45 ± 1.64	<0.001
Change from baseline	−2.76 ± 1.33†††	−1.78 ± 1.14†††	<0.001
FPG (mmol/L)
Baseline	8.96±1.98	8.80 ± 2.12	0.269
Post-intervention	6.33±1.21	7.13 ± 1.83	<0.001
Change from baseline	−2.63±1.24†††	−1.67 ± 1.39†††	<0.001
2hPPG (mmol/L)
Baseline	10.73 ± 2.14	10.52 ± 1.94	0.117
Post-intervention	7.72 ± 1.27	8.18 ± 1.84	<0.001
Change from baseline	−3.02 ± 2.31†††	−2.34 ± 2.03†††	<0.001

Notes: Data are expressed as the mean ± SD. ††† means P<0.001 compared with the baseline. aP-values are for comparisons between the two groups.

Table 5

The Post-Intervention Results of HbA1c in Terms of Age, Sex, Educational, Diabetic Complication, and Comorbidity Status

Characteristics	Intervention Group (n=426)	Control Group (n=423)	aP-value
Gender
Male	6.66(±1.34)	7.50(±1.67)	<0.001
Female	6.64(±1.24)	7.37(±1.60)	<0.001
Age (years)
<60	6.74(±1.35)	7.522(±1.68)	<0.001
≥60	6.54(±1.23)	7.34(±1.60)	<0.001
Education level(n)
Middle school or lower	6.67(±1.32)	7.49(±1.70)	<0.001
High school	6.77(±1.36)	7.32(±1.51)	0.002
College	6.48(±1.18)	7.54(±1.71)	<0.001
Comorbidity status
Hypertension
Yes	6.65(±1.24)	7.87(±1.80)	<0.001
No	6.66(±1.32)	7.36(±1.60)	<0.001
Coronary artery disease
Yes	6.57(±1.08)	6.57(±1.08)	0.005
No	6.66(±1.32)	6.66(±1.32)	<0.001
Diabetic complication
Peripheral angiopathy
Yes	6.61(±1.23)	7.64(±1.51)	<0.001
No	6.68(±1.33)	7.38(±1.68)	<0.001
Peripheral neuropathy
Yes	6.73(±1.42)	7.44(±1.83)	0.008
No	6.64(±1.28)	7.45(±1.60)	<0.001
Diabetic nephropathy
Yes	6.66(±1.19)	7.24(±1.54)	0.031
No	6.66(±1.32)	7.48(±1.66)	<0.001
Diabetic retinopathy
Yes	6.53(±1.38)	7.57(±1.73)	0.008
No	6.67(±1.30)	7.44(±1.64)	<0.001

Notes: Data are expressed as mean ± SD. aP-values are for comparisons between the two groups.

Regarding the rate of target HbA1c achievement, the proportion of patients achieving glycemic control targets of HbA1c < 7.0% and ≤ 6.5% was higher in the intervention than the control group, by 66.4% and 45.6% in the intervention group, and 56.1% and 35.0% in the control group (both P<0.001).

Scores of MDKT, DES-DSF and SDSCA

Higher scores in the MDKT (6.02 ± 3.86 vs 3.37± 2.19, P<0.001), DES-DSF (38.53± 16.70 vs 26.00 ± 18.87, P<0.001), and SDSCA (including diet and exercise; all P<0.001) were obtained with the intervention group, compared with the control group (presented in Table 6).

Table 6

Scores of MDKT, DES-DSF, and SDSCA

Score	Intervention Group (n=426) Mean ± SD	Control Group (n=423) Mean ± SD	P-value a
MDKT
Baseline	13.13±4.08	13.35±3.89	0.430
Post-intervention	19.15±2.64†††	16.71±3.72†††	<0.001
DES-DSF
Baseline	34.00±12.30	34.06±16.19	0.950
Post-intervention	38.53±16.70†††	26.00±18.8†††	<0.001
SDSCA
Diet
Baseline	4.69±1.56	4.80±1.35	0.275
Post-intervention	6.26±0.93†††	5.61±1.20†††	<0.001
Exercise
Baseline	3.56±1.75	3.46±1.73	0.413
Post-intervention	5.27±1.17†††	4.19±1.43†††	<0.001
Blood glucose testing
Baseline	3.23±1.68	3.33±1.71	0.275
Post-intervention	5.20±1.15†††	4.14±1.49†††	<0.001
Foot care
Baseline	3.37±1.59	3.44±1.68	0.527
Post-intervention	5.30±1.14†††	4.12±1.44†††	<0.001
Medication taking
Baseline	5.75±1.02	5.81±1.06	0.387
Post-intervention	6.88±0.34†††	6.24±0.90†††	<0.001
Smoking
Baseline	3.35±1.65	3.34±1.68	0.902
Post-intervention	5.20±1.09†††	4.25±1.39†††	<0.001

Notes: Data are expressed as the mean ± SD. ††† means P<0.001 compared with the baseline. P valuesa are for comparisons between the two groups.

Insulin Doses and Body Weight

No significant differences were observed between the two groups in terms of dose initiation of insulin glargine (seen in Table 7). The insulin dose for the intervention group was significantly higher than that for the control group at the end of study (−0.32±0.12 U/kg vs 0.28±0.10 U/kg, shown in Table 7, P<0.001). We observed no significant differences in weight and BMI at baseline between the groups. After treatment, the body weight (0.46±0.78kg of the IG, 0.40 ± 0.60kg of the IG) and BMI (0.17±0.31kg/m2 of the IG, 0.15±0.22 kg/m2 of the CG) of both groups increased slightly, with no significant differences (P>0.05) between the two groups (seen in Table 7).

Table 7

Insulin Dose, Body Weight, and Safety

Parameter	Intervention Group (n=426) N(%) or Mean ± SD	Control Group (n=423) N(%) or Mean ± SD	P-valuea
Insulin dose (U/kg)
Baseline	0.25±0.11	0.25±0.10	0.983
Post-intervention	0.32±0.12†††	0.28±0.10†††	<0.001
Weight (kg)
Baseline	63.2±8.6	64.3±9.3	0.070
Post-intervention	63.62±8.42	64.68±9.17	0.081
Change from baseline	0.46±0.78†††	0.40±0.60†††	0.242
BMI (kg/m2)
Baseline	23.5±2.3	23.8±2.7	0.111
Post-intervention	23.69±2.21	23.93±2.71	0.141
Change from baseline	0.17±0.31†††	0.15±0.22†††	0.181
Hypoglycemia (%)
Week 0–4	16(3.76)	13(3.07)	0.584
Week 5–8	34(7.98)	29(6.86)	0.532
Week 9–12	38(8.92)	33(7.80)	0.556
Total	88(20.65)	75(17.73)	0.279
URTI (%)
Week 0–12	54(12.7)	48(11.4)	0.552

Notes: Data are expressed as the N(%), or mean ± SD. ††† means P<0.001 compared with the baseline. P-valuesa are for comparisons between the two groups.

Abbreviations: BMI, body mass index; URTI, upper respiratory tract infection.

Safety

Hypoglycemia rates of both groups at baseline and end of the intervention period are shown in Table 7. Hypoglycemic percentages were similar between the two groups (20.65% vs -17.73% for the IG and CG, P=0.279). No major hypoglycemic episodes or serious adverse effects (AE) were reported during the experimental period. The most commonly observed AE was upper respiratory tract infection, with no significant differences between the two groups (12.7% vs 11.4%, P=0.552, seen in Table 7).

Discussion

This study evaluated the efficacy of a combined fasting blood glucose based dosage titration setting and decision supported telephone coaching intervention by the qualified nurses on glycemic control in Chinese patients with T2DM who were treated with insulin glargine. We observed a significant higher reduction (−2.8%) in HbA1c levels of patients in the IG than those (−1.8%) in the CG over 12 weeks of follow-up. There was a study from Asia showed both the patient-led titration and physician-led titration resulted in less mean drop in HbA1c value after 24-week use of glargine (−1.40% and −1.25%) when compared to our patients in the IG.13 Self-managed titration of glargine 300U/mL (Gla-300) was superior to physician-managed titration in terms of HbA1c reduction,24 both were poorer than that of our study. In the BEYOND study on basal insulin therapy from China, higher proportion of patients achieved HbA1c <7.0% in the post-education survey (36.5% vs 27.2%) with reduced HbA1c levels (7.72% vs 8.10%).25 These studies showed the better glucose control may due to education. But these data cannot answer whether the improvements benefited from the general education or the insulin dose titration education. An earlier observational study on basal insulin treatment in China reported mean HbA1c levels of 9.6% at baseline and 7.4% at 6 months,6 the improvements were poorer than our patients in the IG, better than those in the CG. It seems that telephone interview without dosage titration guidance in our study is not effective. The diabetes specialist nurses in the IG kept offering telephone follow-up at key weeks and provide ongoing encouragement, guidance, and support to promote greater treatment efficacy and empowerment for decision changes. The use of decision support to promote patients’ compliance to insulin dose titration is considered an innovative and highly effective strategy for improvement of glycemic control.

Many patients with T2DM continue to achieve suboptimal glycemic control after accepting the BI.6 Once basal insulin is initiated, dose titration is an important factor affecting achievement of target glycemic control.26 Nurse practitioners, physician assistants, pharmacists, and certified diabetes educators play increasingly valuable roles in terms of insulin initiation and titration.27 Incorporation of the services of nurse consultant experts is the key for successful patient treatment with BI, both during hospital stay and after discharge.28 In the Italian Titration Approach Study (ITAS) with insulin Gla-300 in insulin-naïve T2DM, when they wanted to compared the glucose control managed by the patient versus the physician, “nurse assisted” was needed in the patient management group.17 Involvement of nurses as educators seems very useful in BI treatment. In accordance with previous studies,13 the hypoglycemic events and AE in our study are not serious in the titration of BI. Our study demonstrated insulin dose titration by the patient, assisted by the nurse, is effective and useful.

The intervention group reported more improvements in diabetes knowledge in our study. Like other developing country,29 knowledge on diabetes in patients needs to be changed in our country. In a cross-sectional study in Shanghai, patients with higher knowledge scores were more likely to achieve the combined target goal.30 In addition, improvement in empowerment and self-management (including diet, exercise, and blood glucose monitoring) of patients in the IG may contribute to better glucose control. Recent studies have shown that implementation of empowerment strategies among individuals with diabetes was associated with improvements in HbA1c levels, self-management, and distress.31,32 In nationwide survey, Chinese patients with diabetes education achieved better glycemic control than un-educated patients.33 In an outlying city of China, nutritional and eating education also make use.34 Patient understanding of diabetes self-management is critical to optimize safety and enhance outcomes.35 Based on our result and our diabetes education school, we will try to train nurses from different cities and rural areas to be qualified for the education skills that were used in our study. These nurses will contribute to better glucose control of T2DM, in terms of the health system structure in China.

There are some limitations in this study. First, this study was conducted at a single center. Second, although sample size was sufficient to assess primary outcomes, some information of the participants are missing, such as the income level. Third, the 12-week intervention period may not have been sufficient to address maintenance of implemented changes. Nevertheless, our results clearly suggest that decision support of self-titration of basal insulin in outpatients with T2DM is an effective and safe strategy. Further research with longer-term follow-up of patients and collected more detailed data that can be stratified, could be conducted to validate the efficacy of our decision supported intervention.

Conclusions

A combined fasting blood glucose based dosage titration setting and decision supported telephone coaching intervention by diabetes specialist nurses is effective in improving glycemic control with insulin glargine. Patients with T2DM need continued decision supporting, including adequate glycemic target levels and more active insulin dose titration after initiation of insulin therapy.

Impact Statement

The study developed a fasting blood glucose based dosage titration protocol which can assist with clarifying values for decision options.