Stepping Into Lifestyle Changes

Overweight and Obesity Clinical Trial

— SILC  

Official title:

Community-Based Strategies to Reduce Cardiometabolic Disease in the Deep South

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05625321
• Other study ID #: 300009477
• Status: Active, not recruiting
• Phase: N/A
• Start date: March 27, 2023
• Est. completion date: June 30, 2026

Study information

• Verified date: June 2024
• Source: University of Alabama at Birmingham
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to promote healthy weight loss among African American women, age 30 or older, who are pre-diabetic and/or have high blood pressure and who live, work, or worship in select rural communities throughout Alabama and Mississippi. The goal of the study is to help reduce the burden of obesity, diabetes, and high blood pressure for these women and to collect information on the reach, effectiveness, adoption, implementation, maintenance, and cost effectiveness of our two evidence-base weight loss programs.

Description:

This study leverages two evidence-based interventions (EBIs) that have been culturally-adapted for the target population and have previously achieved clinically-relevant weight loss and other clinical outcomes (educational group weight loss intervention) along with improvements in diet and physical activity (home gardening intervention). Combining these EBIs addresses multiple domains (behavioral, personal environment, sociocultural) and levels (individual, interpersonal, community) of influence on risk factors for obesity and other cardiometabolic diseases prevalent in the Deep South. These interventions, delivered by local lay staff and non-academic partners, have a high potential for sustainability; however, there is a need to further evaluate the external validity and implementation-related barriers and facilitators to maximize reach, adoption and implementation. The investigators will employ a pragmatic, multilevel, cluster-randomized, type 1 hybrid effectiveness-implementation trial. A total of 264 Black women (age ≥ 30 years) with overweight or obesity and pre-diabetic or hypertensive from 12 rural counties (6 Alabama, 6 Mississippi) will receive either the combined educational group weight loss intervention plus a home gardening intervention or the educational group weight loss classes alone. The specific aims are to compare interventions on: (1) primary outcomes related to implementation effectiveness (reach, adoption, maintenance of health behaviors), (2) secondary outcomes on clinical effectiveness, and (3) cost effectiveness. Findings will inform discussions with coalition partners to achieve our long-term goal of widely disseminating and sustaining multi-level interventions to reduce the multiple chronic disease burden and health disparities in the Deep South.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 273
• Est. completion date: June 30, 2026
• Est. primary completion date: February 1, 2026
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 30 Years and older

Eligibility

Inclusion Criteria:

• self-identifies as Black and/or African American

• = 30 years old

• a measured BMI >25 kg/m2 and at least one other cardiometabolic risk factor (physician diagnosis of pre-diabetes and/or hypertension within past 2 years)

• lives, works, or worships in one of the 12 intervention communities and expresses no intentions to move outside of that community in the 18 months following enrollment

• a willingness to participate in the study for the 18-months duration.

Exclusion Criteria:

• being or planning to become pregnant during the 18-month study duration

• a baseline blood pressure and/or glucose that is outside of the normal range and a medical provider does not provide clearance to participate

• medical contraindications

Related Conditions & MeSH terms

• High Blood Pressure
• Hypertension
• Overweight
• Overweight and Obesity
• Pre-Diabetes
• Prediabetic State

Intervention

Behavioral:
• Educational Group Weight Loss Classes
Participants will be provided with educational materials on weight loss, and have opportunities to increase their exercise and make changes to their diet.
• Home Gardening Intervention
Participants will receive tools to establish their own home garden, increasing their access to fresh fruits and vegetables.

Locations

Country	Name	City	State
United States	The University of Alabama at Birmingham	Birmingham	Alabama
United States	The University of Mississippi Medical Center	Jackson	Mississippi

Sponsors (2)

Lead Sponsor	Collaborator
University of Alabama at Birmingham	University of Mississippi Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Weight	Changes in Weight, measured in pounds	0, 6, and 12 months
Primary	BMI	Changes in BMI, calculated as a person's weight in kilograms divided by the square of height in meters	0, 6, and 12 months
Primary	Waist Circumference	Changes in waist circumference, measured in centimeters	0, 6, and 12 months
Primary	Dietary Intake	Changes in diet, measured using a questionnaire	0, 6, and 12 months
Secondary	Diastolic and Systolic Blood Pressure	Changes in values over time, using a calibrated automatic sphygmomanometer and following NHLBI protocols	0, 6, and 12 months
Secondary	Fasting Glucose	Changes in glucose readings, collected by finger-stick	0, 6, and 12 months
Secondary	Cholesterol Levels	Changes in LDL and HDL values/ratio, collected by finger-stick	0, 6, and 12 months
Secondary	Physical Activity	Changes in physical activity, measured by the International Physical Activity Questionnaire (IPAQ).; For the IPAQ survey, participants will be asked to indicate if they have completed low (sitting or walking) levels of activity, moderate levels of activity, and/or high levels of activity in the last 7 days.They will also be asked to provide the number of days they do each activity and the time, in minutes, they spend doing the activity.	0, 6, and 12 months
Secondary	Physical Activity	Changes in physical activity, measured by the Stanford Leisure Time Activity Categorical Item (L-cat).; The L-Cat is categorical and responses range from 1-6 with 1 indicating little to no physical activity, and 6 indicating vigorous activity for 5 or more days a week.	0, 6, and 12 months
Secondary	Perceived Quality of Life	Changes in Quality of Life as measured by the EuroQol-5 Dimension survey (EQ-5D-5L). Condition states range from 1-5 with 1 meaning the participant has no problems or symptoms and 5 meaning they have are unable to perform the activity or are extremely impacted by the condition. Self reported health is measured on a 1 to 100 scale with 1 being the worst possible health and 100 being the best possible health.	0, 6, and 12 months