- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05433415
Black Girls Move Physical Activity and Improving Dietary Intake Among Black Adolescent Daughters
Black Girls Move: A Daughter/Mother Intervention to Prevent Obesity by Increasing Physical Activity and Improving Dietary Intake Among Black Adolescent Daughters
Study Overview
Status
Conditions
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60612
- Rush University Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
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
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.
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Baseline, 12 weeks, and 24 weeks
|
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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.
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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
|
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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
|
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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
|
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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
|
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Change from Social Support Scale at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
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A 5-item self-report measure for daughter and mother social support for healthy eating.
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Baseline, 12 weeks, and 24 weeks
|
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Change from Family Assessment Device (FAD) at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
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A 53-item self-report measure of daughter and mother perceptions of family systems.
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Baseline, 12 weeks, and 24 weeks
|
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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
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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
|
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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
|
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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
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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
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A 12-item self-report measure of mother self-efficacy for walking.
|
Baseline, 12 weeks, and 24 weeks
|
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Change from Weight Efficacy Lifestyle Questionnaire at 12 and 24 weeks
Time Frame: Baseline, 12 weeks, and 24 weeks
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A 20-item self-report measure of mother dietary self-efficacy.
|
Baseline, 12 weeks, and 24 weeks
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Monique Reed, Rush University Medical Center
Publications and helpful links
General Publications
- 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.
- 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.
- 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.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Endocrine System Diseases
- Nutrition Disorders
- Metabolic Diseases
- Overnutrition
- Body Weight
- Glucose Metabolism Disorders
- Overweight
- Obesity
- Pathological Conditions, Signs and Symptoms
- Behavior
- Nutritional and Metabolic Diseases
- Signs and Symptoms
- Social Behavior
- Prejudice
- Social Discrimination
- Diabetes Mellitus
- Pediatric Obesity
- Motor Activity
- Racism
Other Study ID Numbers
- R01DK132698 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
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