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Stepping Into Lifestyle Changes (SILC)

Primary Purpose

Overweight and Obesity, Pre-Diabetes, High Blood Pressure

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Educational Group Weight Loss Classes
Home Gardening Intervention
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Overweight and Obesity

Eligibility Criteria

30 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

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

Sites / Locations

  • The University of Alabama at BirminghamRecruiting
  • The University of Mississippi Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Educational Group Weight Loss Classes

Educational Group Weight Loss Classes PLUS Home Gardening Intervention

Arm Description

Participants will participate in a 12-month weight loss program, taught by lay health educators, and designed to promote and encourage healthy weight loss, dietary changes, and increased physical activity. Participants will attend 90-minute sessions weekly for 6 months, bi-weekly for 3 months, and monthly for 3 months.

Participants will receive the educational group weight loss classes PLUS a home gardening intervention. The gardening intervention will be led by local Master Gardeners (MGs) who will help guide participants in setting-up and maintaining their garden.

Outcomes

Primary Outcome Measures

Weight
Changes in Weight, measured in pounds
BMI
Changes in BMI, calculated as a person's weight in kilograms divided by the square of height in meters
Waist Circumference
Changes in waist circumference, measured in centimeters
Dietary Intake
Changes in diet, measured using a questionnaire

Secondary Outcome Measures

Diastolic and Systolic Blood Pressure
Changes in values over time, using a calibrated automatic sphygmomanometer and following NHLBI protocols
Fasting Glucose
Changes in glucose readings, collected by finger-stick
Cholesterol Levels
Changes in LDL and HDL values/ratio, collected by finger-stick
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.
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.
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.

Full Information

First Posted
November 2, 2022
Last Updated
April 4, 2023
Sponsor
University of Alabama at Birmingham
Collaborators
University of Mississippi Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05625321
Brief Title
Stepping Into Lifestyle Changes
Acronym
SILC
Official Title
Community-Based Strategies to Reduce Cardiometabolic Disease in the Deep South
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 27, 2023 (Actual)
Primary Completion Date
February 1, 2026 (Anticipated)
Study Completion Date
June 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham
Collaborators
University of Mississippi Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight and Obesity, Pre-Diabetes, High Blood Pressure

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
264 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Educational Group Weight Loss Classes
Arm Type
Active Comparator
Arm Description
Participants will participate in a 12-month weight loss program, taught by lay health educators, and designed to promote and encourage healthy weight loss, dietary changes, and increased physical activity. Participants will attend 90-minute sessions weekly for 6 months, bi-weekly for 3 months, and monthly for 3 months.
Arm Title
Educational Group Weight Loss Classes PLUS Home Gardening Intervention
Arm Type
Experimental
Arm Description
Participants will receive the educational group weight loss classes PLUS a home gardening intervention. The gardening intervention will be led by local Master Gardeners (MGs) who will help guide participants in setting-up and maintaining their garden.
Intervention Type
Behavioral
Intervention Name(s)
Educational Group Weight Loss Classes
Intervention Description
Participants will be provided with educational materials on weight loss, and have opportunities to increase their exercise and make changes to their diet.
Intervention Type
Behavioral
Intervention Name(s)
Home Gardening Intervention
Intervention Description
Participants will receive tools to establish their own home garden, increasing their access to fresh fruits and vegetables.
Primary Outcome Measure Information:
Title
Weight
Description
Changes in Weight, measured in pounds
Time Frame
0, 6, and 12 months
Title
BMI
Description
Changes in BMI, calculated as a person's weight in kilograms divided by the square of height in meters
Time Frame
0, 6, and 12 months
Title
Waist Circumference
Description
Changes in waist circumference, measured in centimeters
Time Frame
0, 6, and 12 months
Title
Dietary Intake
Description
Changes in diet, measured using a questionnaire
Time Frame
0, 6, and 12 months
Secondary Outcome Measure Information:
Title
Diastolic and Systolic Blood Pressure
Description
Changes in values over time, using a calibrated automatic sphygmomanometer and following NHLBI protocols
Time Frame
0, 6, and 12 months
Title
Fasting Glucose
Description
Changes in glucose readings, collected by finger-stick
Time Frame
0, 6, and 12 months
Title
Cholesterol Levels
Description
Changes in LDL and HDL values/ratio, collected by finger-stick
Time Frame
0, 6, and 12 months
Title
Physical Activity
Description
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.
Time Frame
0, 6, and 12 months
Title
Physical Activity
Description
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.
Time Frame
0, 6, and 12 months
Title
Perceived Quality of Life
Description
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.
Time Frame
0, 6, and 12 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jaimie L Richards, PhD
Phone
205-943-3722
Email
jaimierichards@uabmc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Monica L Baskin, PhD
Email
mbaskin@uabmc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Monica Baskin, PhD
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jaimie Richards, PhD
Phone
205-934-3722
Email
jaimierichards@uabmc.edu
First Name & Middle Initial & Last Name & Degree
Monica Baskin, PhD
Email
mbaskin@uabmc.edu
Facility Name
The University of Mississippi Medical Center
City
Jackson
State/Province
Mississippi
ZIP/Postal Code
39216
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Angela Duck, PhD
Phone
601-815-1949
Email
aduck@umc.edu
First Name & Middle Initial & Last Name & Degree
Charlotte Love
Email
clove1@umc.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Stepping Into Lifestyle Changes

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