Black Girls Move Physical Activity and Improving Dietary Intake Among Black Adolescent Daughters

March 3, 2026 updated by: Rush University Medical Center

Black Girls Move: A Daughter/Mother Intervention to Prevent Obesity by Increasing Physical Activity and Improving Dietary Intake Among Black Adolescent Daughters

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.

Study Overview

Status

Active, not recruiting

Intervention / Treatment

Detailed 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

Study Type

Interventional

Enrollment (Estimated)

120

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Illinois
      • Chicago, Illinois, United States, 60612
        • Rush University Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

12 years to 18 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Description

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Black Girls Move (BGM) Treatment Condition
BGM is guided by the Anti-Racist Public Health Critical Race Praxis with adaptive mechanisms to support Black adolescent females as they navigate a racist society. The BGM treatment condition will include mothers as active participants in all components of the weekly, 12-session intervention to test the impact of actively leveraging the daughter/mother relationship . Participants in our prior research endorsed the importance of daughters and mothers actively engaging in group meetings together on weekends. Participants set PA and diet goals and self-monitor goal attainment. Dyads participate in structured activities designed to facilitate communication, problem solving, role assignment, and relationship quality. Dyads use a variety of videos, role play, discussion, and activities to achieve session outcomes. The sessions are led by trained facilitators who follow a standardized facilitator manual.
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.
Active Comparator: Daughters-Only Comparison Condition (DOCC)
The DOCC runs parallel to the BGM intervention and includes daughters-only group meetings. The DOCC incorporates all components of BGM except Family Systems Theory strategies. Daughters in DOCC will receive PA and diet behavior content based on Anti-Racist Public Health Critical Race Praxis and Social Cognitive Theory with daughter-only group activities. DOCC facilitators will lead group meetings and discussions. All DOCC daughters will self-monitor their progress towards PA goals using Fitbit® and progress towards diet goals using Start Simple with My Plate®.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Actigraph GT3X Device at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, 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
Change from Block Kids 2004 Food Frequency Questionnaire (BKFFQ) at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, 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 Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from 3-Day Physical Activity Recall at 12 and 24 weeks moderate/vigorous physical activity per week
Time Frame: Baseline, 12 weeks, and 24 weeks
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
Change from The Multidimensional Model of Black Identity - Short Form at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
A 27-item self-report measure of daughter and mother racial identity.
Baseline, 12 weeks, and 24 weeks
Change from Child Health Behavior Knowledge Scale at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, 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
Change from Diet and Health Knowledge Survey at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
A 42-item self-report measure of daughter and mother diet knowledge.
Baseline, 12 weeks, and 24 weeks
Change from Physical Activity and Nutrition Self-Efficacy Scale at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, 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
Change from Social Support for Physical Activity at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
An 11-item self-report measure of daughter social support for physical activity.
Baseline, 12 weeks, and 24 weeks
Change from Social Support Scale at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
A 5-item self-report measure for daughter and mother social support for healthy eating.
Baseline, 12 weeks, and 24 weeks
Change from Family Assessment Device (FAD) at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
A 53-item self-report measure of daughter and mother perceptions of family systems.
Baseline, 12 weeks, and 24 weeks
Change fron Quality of Mother Interaction at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
A 14-item self-report measure of daughter perceptions of quality of communication with mother
Baseline, 12 weeks, and 24 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Two-Item Hunger VitalSignTM
Time Frame: Baseline
A 2-item self-report questionnaire evaluating daughter and mother food insecurity in the past 12 months.
Baseline
Change from International Physical Activity Questionnaire at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, 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
Change from 2014 Block Food Frequency Questionnaire at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, 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
Change from Self-Efficacy for Walking Scale at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
A 12-item self-report measure of mother self-efficacy for walking.
Baseline, 12 weeks, and 24 weeks
Change from Weight Efficacy Lifestyle Questionnaire at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
A 20-item self-report measure of mother dietary self-efficacy.
Baseline, 12 weeks, and 24 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 6, 2023

Primary Completion (Actual)

November 30, 2025

Study Completion (Estimated)

May 30, 2026

Study Registration Dates

First Submitted

June 21, 2022

First Submitted That Met QC Criteria

June 22, 2022

First Posted (Actual)

June 27, 2022

Study Record Updates

Last Update Posted (Actual)

March 5, 2026

Last Update Submitted That Met QC Criteria

March 3, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Diabetes Mellitus

Clinical Trials on Black Girls Move

Subscribe