The CREATE Wellness Study
Primary Purpose
Diabetes, Heart Disease, Hypertension
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CREATE Wellness
Usual Care Control
Sponsored by
About this trial
This is an interventional supportive care trial for Diabetes focused on measuring chronic conditions, complex patients, engagement, activation
Eligibility Criteria
Inclusion Criteria:
- Kaiser Permanente Northern California members enrolled in the PHASE disease management program and not meeting all goals of care for the preceding 2 years.
Exclusion Criteria:
- Schizophrenia or personality disorder
- Unable to communicate in English
- Unwilling to participate in group-based in-person program
- Pregnant
- Terminal or debilitating illness
Sites / Locations
- Kaiser Permanente San Jose Sabrina Wood, BA (510) 891-3551 Sabrina.B.Wood@kp.org
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
CREATE Wellness
Usual Care Control
Arm Description
Patients allocated to the intervention arm will receive three group sessions with between visit contacts designed to increase activation and engagement with their care plans. They will also continue to be enrolled in the KP PHASE disease management program.
Patients allocated to the control arm will continue to receive usual care, including disease management within the KP PHASE program.
Outcomes
Primary Outcome Measures
Composite CVD Goal
We will compare the proportion of patients in the two study arms who achieve all three clinical goals of the PHASE disease management program (blood pressure control, HbA1c control (if applicable), and statin prescription) 12 months after enrollment. Risk factor control is defined according to the PHASE disease management program protocol.
Secondary Outcome Measures
Perceived efficacy in patient-physician interactions (PEPPI) - 10 items
We will compare proportion of patients with improvement between baseline and follow-up PEPPI 10-item survey scores between study arms
Effective Consumer Scale (EC-17)
We will compare proportion of patients with improvement between baseline and follow-up EC-17 scores between study arms
Patient Activation Measure (PAM) - 13 items
We will compare proportion of patients with improvement between baseline and follow-up PAM scores between study arms
Full Information
NCT ID
NCT02302612
First Posted
November 21, 2014
Last Updated
October 15, 2018
Sponsor
Kaiser Permanente
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
1. Study Identification
Unique Protocol Identification Number
NCT02302612
Brief Title
The CREATE Wellness Study
Official Title
Multi-Component Behavioral Intervention for Complex Patients With CVD Risk. The Changing Results: Engage and Activate to Enhance Wellness (CREATE Wellness) Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
September 30, 2018 (Actual)
Study Completion Date
September 30, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kaiser Permanente
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Cardiovascular disease (CVD) is the leading cause of death in the U.S. Efforts to improve CVD risk factors often fall short in complex patients with multiple co-morbid conditions, a growing, expensive, and high-risk segment of the U.S. population. The investigators are testing a multi-component behavioral intervention designed to help complex patients with CVD and other concurrent chronic conditions to become more effective agents of their own care.
Detailed Description
Cardiovascular disease (CVD) is the leading cause of death in the U.S. Despite the availability of evidence-based guidelines and efficacious therapies, however, many patients do not achieve the full benefit of CVD risk reduction. In particular, complex patients (defined as those patients who do not respond to current disease management approaches) with multiple concurrent chronic conditions represent a key segment of the population that would benefit from new approaches to care. In response to PA-12-024: Behavioral Interventions to Address Multiple Chronic Conditions in Primary Care, which seeks "practical interventions…to modify behaviors using a common approach" among patients with multiple co-morbidities, the investigators are testing an integrated behavioral intervention designed to improve a core set of chronic disease self-management skills and to overcome common barriers to care engagement encountered by this increasingly important segment of the U.S. adult primary care population. This randomized trial will be conducted within Kaiser Permanente Northern California (KPNC), an integrated care delivery system serving over 3.2 million members, including patients insured through Medicare and state Medicaid programs. The investigators will evaluate the intervention in 3 KPNC primary care practices by enrolling 576 complex patients who have persistently (≥ 2 years) uncontrolled CVD risk factors (e.g. hypertension, hyperlipidemia, diabetes) despite being enrolled in a CVD disease management program. This behavioral intervention is designed to activate and engage patients, identify potentially hidden barriers to care such as alcohol misuse or sub-clinical depression, and to develop individualized care plans that are designed to catalyze more effective primary care management. Randomization will be at the patient-level. The investigators will examine the impact of the intervention on clinical outcomes (control of systolic blood pressure, HbA1c (if with diabetes), statin treatment rates) after 12 months and patient-reported outcomes (patient activation, medication adherence, and mental health status) after 6 months. By focusing on core health skills and care barriers, this patient-focused intervention seeks to enable complex patients to become more effective agents of their own care and to thereby achieve similar clinical benefits as less complex patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Heart Disease, Hypertension, Dyslipidemia
Keywords
chronic conditions, complex patients, engagement, activation
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
647 (Actual)
8. Arms, Groups, and Interventions
Arm Title
CREATE Wellness
Arm Type
Experimental
Arm Description
Patients allocated to the intervention arm will receive three group sessions with between visit contacts designed to increase activation and engagement with their care plans. They will also continue to be enrolled in the KP PHASE disease management program.
Arm Title
Usual Care Control
Arm Type
Active Comparator
Arm Description
Patients allocated to the control arm will continue to receive usual care, including disease management within the KP PHASE program.
Intervention Type
Behavioral
Intervention Name(s)
CREATE Wellness
Intervention Description
Patients allocated to the intervention arm will receive three group sessions with between visit contacts designed to increase activation and engagement with their care plans. They will also continue to be enrolled in the KP PHASE program
Intervention Type
Other
Intervention Name(s)
Usual Care Control
Intervention Description
Patients allocated to the control arm will continue to receive usual care, including disease management within the KP PHASE program.
Primary Outcome Measure Information:
Title
Composite CVD Goal
Description
We will compare the proportion of patients in the two study arms who achieve all three clinical goals of the PHASE disease management program (blood pressure control, HbA1c control (if applicable), and statin prescription) 12 months after enrollment. Risk factor control is defined according to the PHASE disease management program protocol.
Time Frame
12-months
Secondary Outcome Measure Information:
Title
Perceived efficacy in patient-physician interactions (PEPPI) - 10 items
Description
We will compare proportion of patients with improvement between baseline and follow-up PEPPI 10-item survey scores between study arms
Time Frame
6 months
Title
Effective Consumer Scale (EC-17)
Description
We will compare proportion of patients with improvement between baseline and follow-up EC-17 scores between study arms
Time Frame
6 months
Title
Patient Activation Measure (PAM) - 13 items
Description
We will compare proportion of patients with improvement between baseline and follow-up PAM scores between study arms
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Kaiser Permanente Northern California members enrolled in the PHASE disease management program and not meeting all goals of care for the preceding 2 years.
Exclusion Criteria:
Schizophrenia or personality disorder
Unable to communicate in English
Unwilling to participate in group-based in-person program
Pregnant
Terminal or debilitating illness
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard W Grant, MD MPH
Organizational Affiliation
Division of Research, KPNC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kaiser Permanente San Jose Sabrina Wood, BA (510) 891-3551 Sabrina.B.Wood@kp.org
City
San Jose
State/Province
California
ZIP/Postal Code
95119
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
31787053
Citation
Iturralde E, Sterling SA, Uratsu CS, Mishra P, Ross TB, Grant RW. Changing Results-Engage and Activate to Enhance Wellness: A Randomized Clinical Trial to Improve Cardiovascular Risk Management. J Am Heart Assoc. 2019 Dec 3;8(23):e014021. doi: 10.1161/JAHA.119.014021. Epub 2019 Nov 30.
Results Reference
derived
PubMed Identifier
30939290
Citation
Torres DX, Lu WY, Uratsu CS, Sterling SA, Grant RW. Knowing How to Ask Good Questions: Comparing Latinos and Non-Latino Whites Enrolled in a Cardiovascular Disease Prevention Study. Perm J. 2019;23:18-258. doi: 10.7812/TPP/18-258.
Results Reference
derived
PubMed Identifier
29696203
Citation
Miller-Rosales C, Sterling SA, Wood SB, Ross T, Makki M, Zamudio C, Kane IM, Richardson MC, Samayoa C, Charvat-Aguilar N, Lu WY, Vo M, Whelan K, Uratsu CS, Grant RW. CREATE Wellness: A multi-component behavioral intervention for patients not responding to traditional Cardiovascular disease management. Contemp Clin Trials Commun. 2017 Oct 4;8:140-146. doi: 10.1016/j.conctc.2017.10.001. eCollection 2017 Dec.
Results Reference
derived
Learn more about this trial
The CREATE Wellness Study
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