- Research article
- Open Access
- Open Peer Review
A randomized trial of an intervention to improve use and adherence to effective coronary heart disease prevention strategies
© Sheridan et al; licensee BioMed Central Ltd. 2011
- Received: 17 June 2011
- Accepted: 5 December 2011
- Published: 5 December 2011
Efficacious strategies for the primary prevention of coronary heart disease (CHD) are underused, and, when used, have low adherence. Existing efforts to improve use and adherence to these efficacious strategies have been so intensive that they are impractical for clinical practice.
We conducted a randomized trial of a CHD prevention intervention (including a computerized decision aid and automated tailored adherence messages) at one university general internal medicine practice. After obtaining informed consent and collecting baseline data, we randomized patients (men and women age 40-79 with no prior history of cardiovascular disease) to either the intervention or usual care. We then saw them for two additional study visits over 3 months. For intervention participants, we administered the decision aid at the primary study visit (1 week after baseline visit) and then mailed 3 tailored adherence reminders at 2, 4, and 6 weeks. We assessed our outcomes (including the predicted likelihood of angina, myocardial infarction, and CHD death over 10 years (CHD risk) and self-reported adherence) between groups at 3 month follow-up. Data collection occurred from June 2007 through December 2009. All study procedures were IRB approved.
We randomized 160 eligible patients (81 intervention; 79 control) and followed 96% to study conclusion. Mean predicted CHD risk at baseline was 11.3%. The intervention increased self-reported adherence to chosen risk reducing strategies by 25 percentage points (95% CI 8% to 42%), with the biggest effect for aspirin. It also changed predicted CHD risk by -1.1% (95% CI -0.16% to -2%), with a larger effect in a pre-specified subgroup of high risk patients.
A computerized intervention that involves patients in CHD decision making and supports adherence to effective prevention strategies can improve adherence and reduce predicted CHD risk.
Clinical trials registration number
- Coronary Heart Disease Risk
- Coronary Heart Disease Risk Factor
- Coronary Heart Disease Prevention
- Coronary Heart Disease Risk Reduction
- Cholesterol Medication
Efficacious strategies for the primary prevention of coronary heart disease (CHD) (including aspirin, blood pressure and cholesterol medicine, and smoking cessation) reduce the relative risk of CHD events by 20-50% each [1–4]. However, these strategies are underused in clinical practice [5–9] and have low rates of adherence .
Multiple systematic evidence reviews [11–15] and a recent meta-review  have demonstrated that many types of interventions yield small to moderate improvements in medication use and adherence. A common observation, however, is that efficacious interventions are resource-intensive. For instance, the most efficacious interventions for hypertension and cholesterol medication adherence include multiple telephone or in-person counseling sessions delivered by researchers, nurses, or pharmacists with or without the addition of other approaches, such as medication reminders [13, 17]. This led one recent systematic review to conclude that "[current adherence trials] provide little evidence that medication adherence can be improved consistently within the resources available in clinical practice." 
Given limited resources for counseling in clinical practice , alternatives to medication use and adherence counseling must be considered and tested. Two such options are decision aids and automated message libraries. Decision aids employ interactive media to convey health information, help patients clarify their values, and choose health options that are consistent with their values. Automated message libraries generate individually tailored messages that can be used to address specific patient barriers, provide skill building, and give information about ancillary resources . Both have the potential to alleviate provider burden for counseling. However, their role in promoting medication initiation and adherence is largely untested [13, 20–22].
This paper reports on the effects of an intervention designed to promote initiation and adherence to efficacious strategies for the primary prevention of CHD. The intervention includes both a decision aid and a series of automated tailored adherence reminders.
The research team conducted this trial in one university internal medicine practice staffed by 94 physicians, including 18 attendings and 76 residents who were not part of the study team and were eligible for participation. 94% of eligible attendings and 32% of eligible residents attended a study education session, agreed to participate, and allowed their patients to be enrolled. The 1-hour education session encouraged physicians to 1) engage their patients in decisions about CHD prevention and 2) use readily available resources to support adherence. Prior to the education session, physicians gave written informed consent.
Patients were eligible to participate if they were presenting for routine care with an enrolled physician; were between the ages of 40-79 years; had no prior history of cardiovascular disease, diabetes mellitus, or other serious medical condition that limited their life expectancy to less than 5 years; and were at moderate (6-10%) or high risk (> 10%) of CHD over 10 years based on a Framingham risk equation . Patients were excluded if they were presenting for their first visit, had no cholesterol check within the past 18 months, were unable to speak or read English, or had extreme elevations of systolic blood pressure (> 180 mmHg) or cholesterol (> 300 mg/dL).
Patient Recruitment and Enrollment
To recruit patients, study staff identified all age eligible patients returning for visits with enrolled physicians. After reviewing patients' charts, staff mailed recruitment letters to potentially eligible patients and made 3 attempts to call patients who did not "opt-out" of further contact by returning an opt-out postcard. When they reached patients by phone, staff reassessed eligibility and arranged a visit for interested patients.
Patients presented for their initial study visit at least one week prior to a regularly scheduled clinic visit with an enrolled physician. During this visit, patients provided written informed consent; filled out a baseline survey about their demographics, medication use, and plans and self-efficacy for risk reduction; and had their CHD risk factors assessed. Study staff used baseline risk factor assessments to recalculate baseline predicted CHD risk and assure study eligibility.
Randomization and Blinding
Following enrollment, patients were randomized by study staff who accessed an online randomized schedule. Staff told patients only that they were participating in a study about "prevention of heart disease." Physicians were not blinded and saw patients in both the intervention and control group.
The patient-directed intervention consisted of two components: a computerized decision aid to promote initiation of effective CHD prevention strategies, and a series of automated mailed tailored messages to promote adherence. Intervention components were based on the Integrative Theory, Protection Motivation Theory, and Self-Determination Theory as previously described . Further, they were designed at a 6-8th grade reading level and pre-tested using cognitive and usability testing.
The web-based decision aid, called Heart to Heart, had five main functions: it 1) calculated patients' overall risk of CHD events in the next 10 years using a continuous Framingham equation ; 2) educated patients about CHD, their predicted global CHD risk, their risk factors, and the benefits and harms of the most effective risk-reducing strategies (aspirin, cholesterol medication, hypertension medication, and smoking cessation); 3) helped patients clarify their values ; 4) encouraged them to choose risk-reducing strategies that would be acceptable and feasible to them for long-term CHD risk reduction; and 5) coached them to communicate their decisions with their physicians by providing audio clips about ways to overcome common communication barriers. Investigators pilot-tested a previous version of the decision aid  and studied its effects with and without the values clarification section . The coaching portion has not been independently described or tested; a more detailed description is provided in Additional File 1.
Tailored Adherence Messages
Delivery of the Intervention and Surveys
The primary study visit occurred in conjunction with a previously scheduled visit with a participant's usual physician. Participants randomized to the intervention group presented 45 minutes early to their clinic visit to view the decision aid and received a list of their risk factors to get them started. They then self-entered their risk factors and navigated the decision aid on their own using a computer stationed in a private room in the clinic. They had access to research staff at all times for questions about navigation. After viewing the decision aid, participants proceeded to their clinic visit. Participants randomized to the control group did not receive a decision aid and proceeded directly to their clinic visit. Following the clinic visit, a research assistant administered surveys to both intervention and control patients to assess their plans for CHD risk reduction. She then mailed tailored adherence messages to participants in the intervention group approximately 2 weeks, 4 weeks, and 6 weeks after their initial study visit.
Approximately 3 months after the initial study visit, all participants presented for a final study visit and final measures.
Feasibility of Intervention Delivery
Investigators measured the feasibility of intervention delivery by measuring the total time participants spent with the decision aid, whether or not participants required assistance with the decision aid, and the time spent by the research assistant preparing and mailing tailored messages.
Change in Predicted Global CHD Risk
Investigators measured predicted global CHD risk (i.e. risk of angina, myocardial infarction (MI), and CHD death over 10 years) using a well-validated Framingham risk equation , that combined information about a patients' age, gender, smoking history, diabetes status, systolic blood pressure level, total and HDL-cholesterol levels, and left ventricular hypertrophy status in a multivariate equation. Following a precedent set by other researchers [27–30], the research team assumed that the benefits of medication are reasonably captured by entering revised risk factor data into the Framingham equation. Because the effect of aspirin use on CHD risk is not accounted for by the Framingham equation, the team additionally performed a priori-specified modeling of the effects of aspirin by applying a 28% risk reduction  to the calculated CHD risk. This modeling mirrored the modeling of aspirin effects participants saw in the decision aid . To be consistent with a more recent meta-analysis published during the study period , the team also performed a sensitivity analysis, recalculating predicted global CHD risk using a 23% risk reduction for men and a 0% reduction for women. The team also performed sensitivity analyses to determine whether modeling the effects of each CHD risk reducing strategy (aspirin, blood pressure medicine, cholesterol medicine, and smoking cessation) on baseline CHD risk produced different results than recalculating risk as described above. For this analysis, the team multiplied baseline Framingham risk scores by a 28% relative risk reduction for aspirin users, a 25% relative risk reduction for blood pressure medicine users, a 30% relative risk reduction for cholesterol users, and a 50% relative risk reduction for those who stopped smoking [1–4]. Modeling medicine effects may allow investigators to estimate the full benefits of medicines (including those which accrue outside changes in traditional CHD risk factors), however, modeling doesn't adequately account for variance in medicine adherence or the effects of other co-interventions (such as diet and exercise) that impact CHD risk.
Intent to Start Any Effective CHD Risk Reduction Strategy
The research team measured intent to start any effective risk reducing strategy after the primary study visit by asking participants whether or not they planned to initiate aspirin or smoking cessation or initiate or increase blood pressure or cholesterol medication.
Adherence was assessed at 3 months both by self-reported adherence to any new or escalated risk reduction strategy and by self-reported adherence to each individual strategy separately. To verify self-reported adherence, the team then examined changes in CHD biomarkers (including blood pressure and total and HDL cholesterol) among those who self-reported adherence.
CHD Risk Factors
Study staff measured CHD risk factors at baseline and follow-up study visits using well-defined protocols. They measured blood pressure using a non-invasive oscillometric automatic monitor (Omron HEM-907) after the patient had been seated for at least 5 minutes. They averaged three measurements taken at one minute intervals, and defined hypertension as a systolic measurement > 140 mm Hg . They measured serum total and HDL cholesterol levels at the UNC Hospitals' McLendon Laboratory using enzymatic calorimetric testing (Roche Diagnostics Corporation) and defined high cholesterol as a total/HDL cholesterol ratio > 4 . Finally, staff measured smoking status by self-report with confirmation by urine dipstick using the NicAlert test strips (Jant Pharmacal; Encino, CA). A test strip measure of 3 or higher (cotinine concentration > 100 ng/mL) is a positive indication of tobacco use.
Sample size was not based on hypothesis testing, but instead on a reasonable estimation of the sample size necessary to 1) assess the feasibility of the intervention, and 2) determine the effect sizes for the main effects of the intervention.
All data analysis was performed using SAS (Cary, NC) software. To examine the effects of the intervention on primary and secondary efficacy outcomes, including predicted CHD risk, intent to start therapy, self-reported adherence to therapy, and changes in risk factors, investigators used mixed effects models. The study team used a logistic link function for binary outcome variables. They used linear mixed effects models for the continuous outcome variables. Each model included the intervention, education as fixed effects and physicians as random effects. Models on CHD risk factors additionally included baseline measures of the pertinent CHD risk factors as fixed effects. As a check on self-reported adherence, analyses examined the effect of self-reported adherence on CHD risk factors among those who self-reported adherence to blood pressure and cholesterol medication.
To test intent for CHD risk reduction and self-reported adherence as mediators of the intervention's effect on predicted CHD risk, the team used generalized linear mixed effects models and the Baron and Kenny 4-step approach to mediation analysis .
Baseline Participant Characteristics
Total Group (N = 160*)
Intervention Group (N = 81)
Control Group (N = 79)
At least some college
Enrolled in a prescription drug plan
Missed medicine in the last month:
Less than 5% of time
6-25% of time
26-50% of time
51-75% of time
76-95% of time
More than 95% of time
Have potentially modifiable CHD risk factors:
Blood pressure > 140/90 (mmHg)
Total cholesterol/HDL ratio > 4
Not using aspirin, but eligible for it
Mean systolic blood pressure (mmHg)
Mean diastolic blood pressure(mmHg)
Mean total cholesterol (mg/dL)
Mean HDL cholesterol (mg/dL)
Mean predicted CHD risk over 10 yrs
# of possible intervention options for CHD risk:‡
Have self-efficacy to lower at least 1 CHD risk factor
Are planning best evidence interventions§
Feasibility of Intervention Delivery in Practice
Intervention participants spent an average of 12 minutes (range: 1-45 minutes) with the decision aid and were able to navigate it with minimal assistance. Tailored message mailings took research assistants less than 5 minutes per participant.
Effect of the Intervention on Predicted Global CHD Risk
Effect of Heart to Heart Intervention on CHD Risk at Follow-up
Control group (N = 77)
Intervention group (N = 77)
Absolute difference (95% CI) *
Adjusted absolute difference†
(n = 154)
(-3.0% to 0.40%)
(-2.0% to -0.16%)
Moderate risk at baseline (6-10%)
(n = 82)
(-2.4% to 0.51%)
(-1.6% to 0.13%)
High risk at baseline (> 10%)
(n = 72)
(-3.83% to 0.38%)
(-3.2% to 0.39%)
Effect of the Intervention on Intent to Start Any Effective CHD Risk Reducing Strategy
Compared with the control group, participants in the intervention group had significantly higher intentions to start or increase any of the effective CHD risk reducing therapies promoted by our intervention (control 42%, intervention 63%; absolute difference 21%; 95% CI 5% to 37%; adjusted p < 0.01). Increases in overall intent primarily resulted from increases in intent to take aspirin (control 24%, intervention 43%; absolute difference 19%; 95% CI -1 to 39%) and cholesterol medication among those with abnormal cholesterol (control 9%, intervention 39%; absolute difference 30%; 95% CI 14 to 46%).
Effect of the Intervention on Self-reported Adherence to Chosen Risk Reducing Therapies
Proportion of Participants Adhering to their Chosen CHD Risk Reduction Therapy at 3-month Follow-up
Chosen therapy (number in analysis)
Control % (n/N)
Absolute difference (95% CI) (p-value)*
Odds ratio (95% CI)*
Adjusted absolute difference, p-value†
Adjusted odds ratio (95% CI) †
Any chosen therapy promoted by intervention (n = 149) ‡
(8% to 42%)
(p < 0.01)
(1.3 to 5.9)
25%, p < 0.01
(1.4 to 6.9)
Any chosen therapy, including other§ (n = 154)
(4% to 28%)
(p = 0.02)
(1.2 to 4.9)
14%, p = 0.04
(1.0 to 4.8)
Take aspirin (n = 51)
(17% to 55%)
(p < 0.01)
10.9 (2.0 to 59)
39%, p < 0.01
(2.0 to 84)
Take cholesterol medicine (n = 20)
(-28% to 33%)
(0.1 to 12.3)
Take blood pressure medicine (n = 21)
(-9% to 25%)
Stop smoking (n = 13)
Effect of the Intervention on CHD Risk Factors
Effect of Heart to Heart Intervention on CHD Risk Factors at 3-month Follow-up*
Risk factor (number with risk factor at baseline)
Control group Mean (n or n/N)
Intervention group Mean (n or n/N)
Absolute difference (95% CI) †
Adjusted absolute difference (95% CI) ‡
Systolic blood pressure, if HTN (n = 53)
(-14.4 to -0.03)
(-14.3 to 1.2)
Diastolic blood pressure, if HTN (n = 53)
(-4.24 to 4.79)
(-5.2 to 2.80)
Total cholesterol, if abnormal cholesterol (n = 67)
(-14.8 to 28.8)
(-12.0 to 28.1)
HDL, if abnormal cholesterol (n = 67)
(0.08 to 8.53)
(-3.08 to 3.37)
% Smoking, if smokers (n = 13) §
Analyses to confirm self-reported adherence did confirm an effect of self-reported adherence on systolic blood pressure (-8.6 mmHg, 95% CI -14.8 to -2.3) and total cholesterol (-45.6 mg/dL, 95% CI -75.2 to -16.1) in individuals self-reporting adherence to blood pressure and cholesterol medications respectively.
Potential Mediators of Intervention Effect
In mediation analysis, adding intentions for CHD risk reduction to the model testing the relationship between the intervention and predicted CHD risk reduced the difference in predicted CHD risk by 0.18 absolute percentage points, while adding self-reported adherence to the model reduced the difference in predicted CHD risk by 0.22 absolute percentage points.
At 3-month follow-up, a computerized intervention designed to promote CHD prevention medication use and adherence increased self-reported adherence by 25 percentage points and reduced 10-year predicted global CHD risk by 1.1 percentage points, with a larger effect seen in a pre-specified high risk sub-group. The effect on predicted CHD risk was mediated, in part, by intent to reduce CHD risk and by self-reported adherence.
These findings are similar to those reported in previous studies of more resource-intensive interventions for CHD prevention. For instance, multiple systematic reviews have shown 10-25 absolute percentage point increases in adherence, with the largest effects in studies using multiple telephone or in-person counseling sessions . Furthermore, a recent systematic evidence review found that global risk information, in repeated doses or with repeated counseling, reduced predicted CHD risk by 0.2 to 2 absolute percentage points . What is noteworthy about this study is that it achieved its effects using a computerized decision aid and automated message library to perform the functions of education and counseling.
Also noteworthy about this study are the reported effects of the intervention on aspirin adherence. Given the risk based recommendations for aspirin therapy  and individuals' desire for inexpensive, familiar, trusted interventions , it is not surprising that the intervention had its greatest effect on initiation of and adherence to aspirin.
What is somewhat surprising about this study is the apparent lack of effect of our intervention on cholesterol-lowering medication adherence. Not only are cholesterol guidelines risk-based, but a recent systematic review  found consistent reductions in total and LDL cholesterol in patients who received predicted CHD risk information and counseling. We suspect the lack of effect of the intervention on cholesterol is due in large part to the small number of participants (n = 20) choosing, initiating and adhering to cholesterol therapy, which limits the ability to detect any effect.
To better understand the effects of our intervention, investigators performed mediation analyses. These analyses suggest that both intent to reduce CHD risk and self-reported adherence to medications partially mediate reductions in 10-year predicted CHD risk. The proportional effects, however, are small (~20%), raising questions about other potential mediators such as diet and physical activity.
Interpretation of these findings should proceed with acknowledgement of the following limitations. First, this was a relatively small study not designed to look at subgroup effects. Subgroup analyses are small and underpowered, and should be used only for hypothesis generation. Second, physicians saw patients in both the intervention and control groups, which may have resulted in contamination between study groups. This may have reduced the effects of our intervention. Third, the effect of the intervention was diluted by the presence of participants (10%) who had no options for CHD risk reduction. Fourth, investigators measured adherence primarily by self-report (although with correlation with biomarkers). Based on studies comparing objective and subjective measures of adherence , it is likely we slightly overestimated adherence. Fifth, although randomization is expected to result in equally distributed characteristics between the intervention and control groups, the difference in education between groups raises questions about unmeasured confounders. Sixth, the study team conducted this study in one academic medicine clinic, and results might not generalize to other clinics, physicians, or patient populations. Finally, this was a short-term study with only 3 months of follow-up; longer follow-up likely would affect results.
Limitations aside, the results of this study preliminarily suggest that an adherence intervention employing a computerized decision aid and automated adherence messages can increase patients' adherence and reduce CHD risk. This result should be confirmed in larger and broader populations with longer term follow-up. Additionally, future studies should consider additional implementation issues, such as cost, cost-effectiveness, and alternate mechanisms of delivery (e.g. via electronic health record).
Acknowledgements and Funding
The research reported in this publication was supported in part by a grant from the American Heart Association (grant number 0530164N), the National Heart Lung and Blood Institute (grant number 1 K23 HL074375), and the National Cancer Institute (grant number K05 CA129166). The funding agreement ensured the authors' independence in designing the study, interpreting the data, writing, and publishing the report. The authors would like to thank Amy Turner and the Communication for Health Applications and Interventions (CHAI) Core (grant number DK 56350) for help with intervention development; Megan Diehl, JB Lykes, Danielle Lungelow, and Hossein Maymani for help with data collection; and the Working Group on Risk, Communication, and Healthcare Decision Making for comments on prior drafts of this manuscript. Preliminary data from this study were presented at the national Society of General Internal Medicine meeting in May 2009.
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