CREATION Health Lifestyle Intervention
- Conditions
- Cardiovascular Risk
- Interventions
- Behavioral: Behavioral Intervention
- Registration Number
- NCT03412175
- Lead Sponsor
- AdventHealth
- Brief Summary
The CREATION Health Lifestyle Intervention (CHLI) will study the effect of a lifestyle intervention program on the cardiovascular risk profile (blood pressure, BMI, and Hemoglobin A1C) of participants diagnosed with hypertension and/or type 2 diabetes.
- Detailed Description
The CREATION Health Lifestyle intervention is targeted at improving the cardiovascular risk profiles (blood pressure, BMI, and Hemoglobin A1C) of participants diagnosed with hypertension and/or type 2 diabetes. The intervention is designed to address the whole person and is based on the CREATION Health framework. Participants in the lifestyle intervention arm will receive 6 individual visits with a CREATION Health Specialist over a 3 month period, and one follow up visit at 6 months. The visits include one 2 hour-long initial assessment, four 60-minute motivational interview sessions, and two 60-minute reassessments. Visits will focus on tailoring the intervention care plan to each individual, goal-setting, action plans, self-monitoring, identification of personal and social barriers to change, self-regulatory techniques, and provision of psychosocial support using motivational interviewing techniques. Using the CREATION Health framework, the CREATION Health Specialist will educate the participant and make recommendations for lifestyle modifications that lead to reduction in cardiovascular disease risk by focusing on: reduced energy intake, primarily via lowering fat intake to \<30% of caloric intake; increased physical activity to 150 minutes per week; smoking cessation; limited sodium intake; and limited alcohol intake.
Intervention fidelity will be determined by tracking the content of visits on encounter forms. There will also be a quality assurance assessment by audio-taping a select number of CHS-patient visits. The audiotapes will be reviewed by the study team and CHS for adherence to study intervention protocols.
Participants in the intervention group will also receive a health journal to document progress and a CREATION Health workbook that introduces the CREATION Health framework in more detail. The workbook explains each concept of the CREATION Health framework: Choice; Rest; Environment; Activity; Trust in God; Interpersonal relationships; Outlook; and Nutrition. Participants in the intervention group will receive a CREATION Health One-sentence Journal.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 184
- Diagnosis of Type 2 Diabetes, fasting glucose >125, or Hg A1C >6.5% and/or
- Diagnosis of Hypertension
- Age 18 or older
- Agree to participate in all aspects of study intervention and assessments
- Able to give informed consent
- Access to home phone or mobile phone
- Current use of oral corticosteroids
- Current use of psychotropics for psychosis or bipolar disorder
- Use of weight-loss medication in the past 3 months
- Psychiatric hospitalization in the past 3 years
- Cancer diagnosis or treatment in the past 3 years
- History of MI, CABG, stroke, PTCA, balloon pump, etc in past 2 years
- Hemoglobin A1C 12% or more on two occasion in the past 6 months
- Pregnancy
- Severe debilitating medical condition that would interfere with completion of intervention
- Unable to speak, read, and understand English
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Behavioral Intervention Behavioral Intervention Participants in the lifestyle intervention arm will receive 6 individual visits with a CREATION Health Specialist over a 3 month period, and one follow up visit at 6 months. The visits include one 2 hour-long initial assessment, four 60-minute motivational interview sessions, and two 60-minute reassessments. Visits will focus on tailoring the intervention care plan to each individual, goal-setting, action plans, self-monitoring, identification of personal and social barriers to change, self-regulatory techniques, and provision of psychosocial support using motivational interviewing techniques.
- Primary Outcome Measures
Name Time Method Hemoglobin A1C 6 months A reduction of Hemoglobin A1C in participants diagnosed with Type II Diabetes Mellitus to less than 6% as measured by fasting blood work
Blood Pressure 6 months A 6 mm Hg reduction in systolic blood pressure/diastolic blood pressure as measured in clinic in participants diagnosed with Hypertension
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Florida Hospital
🇺🇸Orlando, Florida, United States