Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05433415
Other study ID # R01DK132698
Secondary ID R01DK132698
Status Recruiting
Phase N/A
First received
Last updated
Start date March 6, 2023
Est. completion date April 2025

Study information

Verified date November 2023
Source Rush University Medical Center
Contact Monique Reed, PhD
Phone 3129428349
Email monique_reed@rush.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Black Girls Move is a school-linked daughter/mother physical activity and dietary behavior program, with 9th and 10th grade students. This program is designed to prevent obesity in Black adolescent females and thus aligns with the NIH mission to enhance health, lengthen life, and reduce illness and disability. This project is relevant to public health because it holds the potential to reduce population health disparities impacted by structural racism.


Description:

Black female adolescents are at increased risk for obesity-related morbidity and mortality as adults compared to non-Hispanic White female adolescents. Interventions to prevent obesity in Black female adolescents that leverage the relationship of the daughter/mother dyad have received limited attention. Studies that do include mothers tend to use theoretical frameworks that do not explicitly build on this important family relationship and have not included mothers' active participation. Additionally, these studies do not include girls over the age of 12. In response, the investigators developed Black Girls Move, a school-based obesity prevention intervention that addresses these limitations in the extant literature. The investigators conducted focus groups with daughter/mother dyads to identify practical, cultural, and age-appropriate strategies for improving physical activity (PA) and dietary behaviors in Black adolescent daughters (grades 9-10, ages 14-17). Black Girls Move consists of 12 weekly group sessions of daughter/mother dyads in which participants set individualized PA and dietary goals. Black Girls Move incorporates content and processes derived from asset-based anti-racist Public Health Critical Race Praxis, Family Systems Theory, and Social Cognitive Theory. Specific aims are to determine the efficacy of Black Girls Move compared to daughters-only comparison condition on change in PA and dietary intake, and the impact of Black Girls Move compared to daughters-only on theoretical mechanisms of change (racial identity, daughter/mother relationship, social cognitions) assessed by self-report measures. The design is a 12-week pre-test/post-test, randomized controlled trial. The investigators will recruit 24 daughter/mother dyads at each of 8 schools for a total sample size of 192 daughter/mother dyads (total 384 participants). Within school, each dyad will be randomized to either Black Girls Move or daughters-only comparison condition (12 per condition). All daughters and all mothers (Black Girls Move daughter/mother dyads and daughters-only comparison condition daughter/mother dyads) complete assessments (e.g., PA, diet, family measures) at baseline, post-intervention, and 3-months post-intervention. The investigators recognize that there are potential validity threats associated with within school student randomization. The investigators will collect data to assess the degree to which these potential threats are pertinent. The long-term goal of this research is to decrease disparities in obesity and associated comorbidities in Black women. The findings may inform future large scale R01 studies of BGM in Black daughter/mother dyads


Recruitment information / eligibility

Status Recruiting
Enrollment 384
Est. completion date April 2025
Est. primary completion date July 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 12 Years to 18 Years
Eligibility Inclusion Criteria for daughters are: - English speaking; - Black; - grade 9 or 10; - daily access to the internet outside of school and/or work through an iOS or android smart phone, tablet, or personal computer; - either high-normal weight (between =50th and <85th percentile for age and gender) or overweight (between =85th and <95th percentile for age and gender) as the purpose of this study is weight maintenance and obesity prevention in at-risk daughters rather than obesity treatment; 98 and - have either a poor diet, (defined as consuming <1 vegetable or <1 fruit per day) 99 or inadequate PA (defined as < 60 minutes per day, 7 days per week). 99,100 Inclusion criteria for mothers are: - English-speaking; - Black; - co-residing biological mother or mother-figure and legal guardian of the participating daughter; - the person primarily responsible for meals in the household; and - access to the internet through an iOS or android smart phone, tablet or personal computer. In a longitudinal study of 480 adults, 84% of adults with obesity were adolescents with high normal weight status (=50th and <85th percentile). National data on cell phone ownership show that 81% of Black students and 68% of Black parents own a smart phone Exclusion Criteria: The exclusion criteria for both daughters and mothers includes: - having conditions/procedures that prevent the oral consumption of foods (e.g., gastric feeding tubes); - presence of physical limitations that would preclude participation in the PA activity components of the intervention; - altered dietary intake (e.g., pregnancy, eating or metabolic disorders except for type 1 or type 2 diabetes); and - at baseline physical assessment, participants screened for uncontrolled blood pressure (systolic > 130, diastolic >80 for daughters; and systolic >160, diastolic >100 for mothers) will be eligible only with a healthcare provider release. - participants with diagnosed type 1 or 2 diabetes will be eligible for participation only with a healthcare provider release. - mothers will be screened for cardiovascular disease and musculoskeletal risk factors with the 7-item Physical Activity Readiness Questionnaire. Mothers that answer 'yes' to any item on the Physical Activity Readiness Questionnaire will be eligible only with a healthcare provider release. Daughters or mothers who are asked to provide healthcare provider release will be referred to the Chicago Department of Public Health if they do not have a primary care provider. To be eligible to participate in either condition, both the daughter and her mother must be willing and eligible to participate in the study.

Study Design


Intervention

Behavioral:
Black Girls Move
Goal setting and monitoring. All BGM daughters will self-monitor their progress towards PA goals using a PA device, Fitbit®. Additionally, BGM daughters will self-monitor their progress towards diet goals using a mobile application, Start Simple with My Plate®. Further, all BGM mothers will use Fitbit® and Start Simple with My Plate® for self monitoring, however, mothers' data will not be analyzed for this study. Since the daughter/ mother relationship is critical to achieving behavioral change, BGM mothers will utilize Fitbit® and Start Simple with My Plate® as a mechanism to communicate, problem solve and support daughters' behavioral goals.BGM is situated within the contexts of environmental, cultural, interpersonal, and developmental factors impacted by structural racism. Intentionally engaging mothers and daughters in an asset based program provides a framework for mothers to model responses to structural racism i.e. racial socialization.

Locations

Country Name City State
United States Rush University Medical Center Chicago Illinois

Sponsors (4)

Lead Sponsor Collaborator
Rush University Medical Center National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH), University of Illinois at Chicago

Country where clinical trial is conducted

United States, 

References & Publications (3)

Reed M, Julion W, McNaughton D, Wilbur J. Preferred intervention strategies to improve dietary and physical activity behaviors among African-American mothers and daughters. Public Health Nurs. 2017 Sep;34(5):461-471. doi: 10.1111/phn.12339. Epub 2017 Jun 22. — View Citation

Reed M, Wilbur J, Schoeny M. Parent and African American Daughter Obesity Prevention Interventions: An Integrative Review. J Health Care Poor Underserved. 2015 Aug;26(3):737-60. doi: 10.1353/hpu.2015.0103. — View Citation

Reed M, Wilbur J, Tangney CC, Miller AM, Schoeny ME, Webber-Ritchey KJ. Development and Feasibility of an Obesity Prevention Intervention for Black Adolescent Daughters and Their Mothers. J Healthy Eat Act Living. 2021 Apr 1;1(2):94-107. eCollection 2021. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Two-Item Hunger VitalSignTM A 2-item self-report questionnaire evaluating daughter and mother food insecurity in the past 12 months. Baseline
Other Change from International Physical Activity Questionnaire at 12 and 24 weeks A 27-item self-report measure of mother physical activity. Activities pertain to job (7), transportation (6), household (6), recreation (6), and sitting (2). Participants indicate frequency (days), duration (hours/minutes), and intensity (moderate to vigorous) over past 7days. Baseline, 12 weeks, and 24 weeks
Other Change from 2014 Block Food Frequency Questionnaire at 12 and 24 weeks A 127-item self-report measure of mother dietary behavior. Items similar to BKFFQ with additional items to adjust for fat, protein, carbohydrate, sugar, and whole grain content Baseline, 12 weeks, and 24 weeks
Other Change from Self-Efficacy for Walking Scale at 12 and 24 weeks A 12-item self-report measure of mother self-efficacy for walking. Baseline, 12 weeks, and 24 weeks
Other Change from Weight Efficacy Lifestyle Questionnaire at 12 and 24 weeks A 20-item self-report measure of mother dietary self-efficacy. Baseline, 12 weeks, and 24 weeks
Primary Change from Actigraph GT3X Device at 12 and 24 weeks Objective measure of daughter and mother daily steps and activity counts. PA levels operationalized as moderate (1500-2600 counts/30 secs) or vigorous (>2600 count/30 secs). Device worn for one week during waking hours Baseline, 12 weeks, and 24 weeks
Primary Change from Block Kids 2004 Food Frequency Questionnaire (BKFFQ) at 12 and 24 weeks A 72-item self-report measure of daughter dietary behavior over the past week. Participants indicate frequency of consumption of food/beverages on a 6-point scale (none to every day). Baseline, 12 weeks, and 24 weeks
Secondary Change from 3-Day Physical Activity Recall at 12 and 24 weeks moderate/vigorous physical activity per week A 59-item self-report measure of daughter physical activity. Participants recall 59 physical activity activities in the past 3 days. Each day divided into 34, 30-minute blocks from 7 am to midnight. Activities rated as light, moderate, hard, or very hard. Baseline, 12 weeks, and 24 weeks
Secondary Change from The Multidimensional Model of Black Identity - Short Form at 12 and 24 weeks A 27-item self-report measure of daughter and mother racial identity. Baseline, 12 weeks, and 24 weeks
Secondary Change from Child Health Behavior Knowledge Scale at 12 and 24 weeks A 9-item self-report measure of daughter and mother physical activity knowledge related to cardiovascular benefits of exercise. Baseline, 12 weeks, and 24 weeks
Secondary Change from Diet and Health Knowledge Survey at 12 and 24 weeks A 42-item self-report measure of daughter and mother diet knowledge. Baseline, 12 weeks, and 24 weeks
Secondary Change from Physical Activity and Nutrition Self-Efficacy Scale at 12 and 24 weeks An 11-item self-report measure of daughter self-efficacy for physical activity (3 items) and nutrition (8 items) behaviors. Baseline, 12 weeks, and 24 weeks
Secondary Change from Social Support for Physical Activity at 12 and 24 weeks An 11-item self-report measure of daughter social support for physical activity. Baseline, 12 weeks, and 24 weeks
Secondary Change from Social Support Scale at 12 and 24 weeks A 5-item self-report measure for daughter and mother social support for healthy eating. Baseline, 12 weeks, and 24 weeks
Secondary Change from Family Assessment Device (FAD) at 12 and 24 weeks A 53-item self-report measure of daughter and mother perceptions of family systems. Baseline, 12 weeks, and 24 weeks
Secondary Change fron Quality of Mother Interaction at 12 and 24 weeks A 14-item self-report measure of daughter perceptions of quality of communication with mother Baseline, 12 weeks, and 24 weeks
See also
  Status Clinical Trial Phase
Completed NCT03743779 - Mastering Diabetes Pilot Study
Completed NCT03786978 - Pharmaceutical Care in the Reduction of Readmission Rates in Diabetes Melitus N/A
Completed NCT01804803 - DIgital Assisted MONitoring for DiabeteS - I N/A
Completed NCT05039970 - A Real-World Study of a Mobile Device-based Serious Health Game on Session Attendance in the National Diabetes Prevention Program N/A
Completed NCT04507867 - Effect of a NSS to Reduce Complications in Patients With Covid-19 and Comorbidities in Stage III N/A
Completed NCT04068272 - Safety of Bosentan in Type II Diabetic Patients Phase 1
Completed NCT03243383 - Readmission Prevention Pilot Trial in Diabetes Patients N/A
Completed NCT03730480 - User Performance of the CONTOUR NEXT and CONTOUR TV3 Blood Glucose Monitoring System (BGMS) N/A
Recruiting NCT02690467 - Efficacy, Safety and Acceptability of the New Pen Needle 34gx3,5mm. N/A
Completed NCT02229383 - Phase III Study to Evaluate Safety and Efficacy of Added Exenatide Versus Placebo to Titrated Basal Insulin Glargine in Inadequately Controlled Patients With Type II Diabetes Mellitus Phase 3
Completed NCT06181721 - Evaluating Glucose Control Using a Next Generation Automated Insulin Delivery Algorithm in Patients With Type 1 and Type 2 Diabetes N/A
Completed NCT05799976 - Text Message-Based Nudges Prior to Primary Care Visits to Increase Care Gap Closure N/A
Recruiting NCT04489043 - Exercise, Prediabetes and Diabetes After Renal Transplantation. N/A
Withdrawn NCT03319784 - Analysis for NSAID VS Corticosteroid Shoulder Injection in Diabetic Patients Phase 4
Completed NCT03542084 - Endocrinology Auto-Triggered e-Consults N/A
Completed NCT02229396 - Phase 3 28-Week Study With 24-Week and 52-week Extension Phases to Evaluate Efficacy and Safety of Exenatide Once Weekly and Dapagliflozin Versus Exenatide and Dapagliflozin Matching Placebo Phase 3
Recruiting NCT05544266 - Rare and Atypical Diabetes Network
Completed NCT01892319 - An International Non-interventional Cohort Study to Evaluate the Safety of Treatment With Insulin Detemir in Pregnant Women With Diabetes Mellitus. Diabetes Pregnancy Registry
Completed NCT05031000 - Blood Glucose Monitoring Systems: Discounter Versus Brand N/A
Recruiting NCT04039763 - RT-CGM in Young Adults at Risk of DKA N/A