CHLI: CREATION Health Lifestyle Intervention

Sponsor
AdventHealth (Other)
Overall Status
Completed
CT.gov ID
NCT03412175
Collaborator
(none)
184
1
2
27
6.8

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Behavioral Intervention
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
184 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
CREATION Health Lifestyle Intervention
Study Start Date :
May 1, 2016
Actual Primary Completion Date :
Aug 1, 2018
Actual Study Completion Date :
Aug 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: 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.

Behavioral: Behavioral Intervention
The CREATION Health Specialist (CHS) will review with the participant his/her biometrics, assessments, and surveys. The CHS will identify the participant's strengths and weaknesses thereby tailoring the intervention care plan to the participant. Together the participant and CHS will work on goal-setting, action plans, self-monitoring, identification of personal and social barriers to change, and self-regulatory techniques.

No Intervention: Control Group

Participants in the control group will receive usual care as provided by their primary care physician. Participants in the control group will complete biometrics, surveys, and assessments at Visits 0, 5 and 6.

Outcome Measures

Primary Outcome Measures

  1. 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

  2. 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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Diagnosis of Type 2 Diabetes, fasting glucose >125, or Hg A1C >6.5% and/or

  2. Diagnosis of Hypertension

  3. Age 18 or older

  4. Agree to participate in all aspects of study intervention and assessments

  5. Able to give informed consent

  6. Access to home phone or mobile phone

Exclusion Criteria:
  1. Current use of oral corticosteroids

  2. Current use of psychotropics for psychosis or bipolar disorder

  3. Use of weight-loss medication in the past 3 months

  4. Psychiatric hospitalization in the past 3 years

  5. Cancer diagnosis or treatment in the past 3 years

  6. History of MI, CABG, stroke, PTCA, balloon pump, etc in past 2 years

  7. Hemoglobin A1C 12% or more on two occasion in the past 6 months

  8. Pregnancy

  9. Severe debilitating medical condition that would interfere with completion of intervention

  10. Unable to speak, read, and understand English

Contacts and Locations

Locations

Site City State Country Postal Code
1 Florida Hospital Orlando Florida United States 32804

Sponsors and Collaborators

  • AdventHealth

Investigators

  • Principal Investigator: Patricia Robinson, Center for CREATION Health Research

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
AdventHealth
ClinicalTrials.gov Identifier:
NCT03412175
Other Study ID Numbers:
  • 878401
First Posted:
Jan 26, 2018
Last Update Posted:
Aug 29, 2018
Last Verified:
Aug 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 29, 2018