Testing the effectiveness of a mindfulness-based intervention to reduce emotional distress in outpatients with diabetes (DiaMind): design of a randomized controlled trial.
Study Goal
The researchers aimed to test the effectiveness of a diabetes-specific mindfulness intervention in reducing emotional distress and improving quality of life, self-esteem, self-care, and clinical outcomes in patients with diabetes.
Results Summary
The study hypothesized significant improvements in emotional well-being, quality of life, dispositional mindfulness, self-esteem, self-care, and blood pressure in the mindfulness group compared to the control group, but results were not yet available at the time of the abstract.
Population
Outpatients with diabetes experiencing low emotional well-being.
Effective Dosage
Not specified
Duration
Intervention duration not specified, but follow-up was planned for six months post-intervention.
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
a new diabetes-specific, mindfulness-based psychological intervention | decrease | emotional distress | patients with diabetes | - | test the effectiveness | #1 |
a new diabetes-specific, mindfulness-based psychological intervention | increase | quality of life | patients with diabetes | - | improving | #2 |
a new diabetes-specific, mindfulness-based psychological intervention | increase | dispositional mindfulness | patients with diabetes | - | improving | #3 |
a new diabetes-specific, mindfulness-based psychological intervention | increase | self-esteem | patients with diabetes | - | improving | #4 |
a new diabetes-specific, mindfulness-based psychological intervention | increase | self-care | patients with diabetes | - | with regard to | #5 |
a new diabetes-specific, mindfulness-based psychological intervention | increase | clinical outcomes | patients with diabetes | - | with regard to | #6 |
the mindfulness program | increase | emotional well-being | patients with diabetes | - | will improve significantly more | #7 |
the mindfulness program | increase | quality of life | patients with diabetes | - | will improve significantly more | #8 |
the mindfulness program | increase | dispositional mindfulness | patients with diabetes | - | will improve significantly more | #9 |
the mindfulness program | increase | self-esteem | patients with diabetes | - | will improve significantly more | #10 |
the mindfulness program | increase | self-care | patients with diabetes | - | will improve significantly more | #11 |
the mindfulness program | decrease | blood pressure | patients with diabetes | - | will improve significantly more | #12 |
BACKGROUND: Approximately 20-40% of outpatients with diabetes experience elevated levels of emotional distress, varying from disease-specific distress to general symptoms of anxiety and depression. The patient's emotional well-being is related to other unfavorable outcomes, like reduced quality of life, sub-optimal self-care, impaired glycemic control, higher risk of complications, and increased mortality rates. The purpose of this study is to test the effectiveness of a new diabetes-specific, mindfulness-based psychological intervention. First, with regard to reducing emotional distress; second, with respect to improving quality of life, dispositional mindfulness, and self-esteem of patients with diabetes; third, with regard to self-care and clinical outcomes; finally, a potential effect modification by clinical and personality characteristics will be explored. METHODS/DESIGN: The Diabetes and Mindfulness study (DiaMind) is a randomized controlled trial. Patients with diabetes with low levels of emotional well-being will be recruited from outpatient diabetes clinics. Eligible patients will be randomized to an intervention group or a wait-list control group. The intervention group will receive the mindfulness program immediately, while the control group will receive the program eight months later. The primary outcome is emotional distress (anxiety, stress, depressive symptoms), for which data will be collected at baseline, four weeks, post intervention, and after six months follow-up. In addition, self-report data will be collected on quality of life, dispositional mindfulness, self-esteem, self-care, and personality, while complications and glycemic control will be assessed from medical files and blood pressure will be measured. Group differences will be analyzed with repeated measures analysis of covariance.The study is supported by grants from the Dutch Diabetes Research Foundation and Tilburg University and has been approved by a medical ethics committee. DISCUSSION: It is hypothesized that emotional well-being, quality of life, dispositional mindfulness, self-esteem, self-care, and blood pressure will improve significantly more in the mindfulness group compared to the control group. Results of this study can contribute to a better care for patients with diabetes with lowered levels of emotional well-being. It is expected that the first results will become available in 2012. TRIAL REGISTRATION: Dutch Trial Register NTR2145.