Behavioral Activation Therapy for Both Depression and Diabetes Vs. Diabetes Alone Delivered Via Group Visits
Completed · Not applicable
Conditions studied: Diabetes, Depression
In brief
The purpose of this study is to determine whether group visits with added behavioral activation (BA) for depression will have a greater clinical impact than our standard group visits without BA for depression in reducing the risk of future coronary events as measured by the United Kingdom Prospective Diabetes Study (UKPDS) risk engine and depression symptoms as measured by Patient Health Questionnaire-9 (PHQ-9) after 6 months.
Key facts
- Study ID
- NCT02027259
- Run by
- Providence VA Medical Center
- People needed
- 52
- Starts
- 2012-01-19
- Expected to finish
- 2015-10-02
- Last updated by the study team
- 2021-10-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Clinical diagnosis of type 2 diabetes
- Clinical diagnosis of depression
- PHQ-9 score ≥10 for depressive symptoms
- >= 18 years old
- a most recent HbA1c ≥8.0% within the previous 12 months in the chart; and
- have 1 or more of the following modifiable CVD risk factors not at target goals, defined as:
- current smoker (any cigarette smoking <30 days),
- blood pressure >130/80 mm Hg, documented at least twice in the last 6 months
- LDL cholesterol >100 mg/dL within the last 12 months.
You may not qualify if…
- Inability to attend the group sessions
- active psychosis of any type or organic brain injury that precludes DM self- care
- type 1 diabetes as documented in the medical chart
- pregnancy
- actively suicidal and /or
- end-stage medical illness (e.g. metastatic cancer, awaiting organ transplant)
- Patients currently enrolled in DM group programs that include medication titration within the group setting would not be eligible due to co- intervention.
Where it is running
- Providence VAMC — Providence, Rhode Island, United States
Full record on ClinicalTrials.gov
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