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My Baby My Move A Community Wellness Intervention

My Baby My Move A Community Wellness Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04294095
Acronym
MBMM+
Enrollment
68
Registered
2020-03-03
Start date
2020-09-01
Completion date
2022-01-01
Last updated
2023-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gestational Weight Gain

Brief summary

My Baby, My Move+ (2019-2021) is a peer-led wellness intervention which aims to reduce excessive gestational weight gain (EGWG) by targeting prenatal physical activity, mood, and sleep quality. Up to 50% of pregnant women in the U.S. gain weight in excess of the Institute of Medicine guidelines. EGWG leads to poor maternal and child outcomes. It also sets the stage for long-term overweight/obesity for both mother and child. The MBMM+ intervention is an example of a theoretically-based prenatal physical activity intervention that targets these outcomes. Up to 100 pregnant women (50 intervention arm, 50 control arm) will be recruited from the University of Colorado Clinics. Women in the intervention arm will participate in the 12-week MBMM+ intervention. Leiferman and her team propose to develop and test the feasibility and sustainability of the MBMM+ intervention to instill good healthy habits (e.g., prenatal physical activity, good sleep hygiene, stress management) during and beyond pregnancy. Findings from this study will be used to inform a future, large randomized trial.

Detailed description

Intervention Group: The MBMM+ intervention is designed to promote the engagement in physical activity and takes into account barriers among pregnant women cited in our formative work such as lack of knowledge and skills, body changes and discomfort, feeling limited, and lack of social support. Uniquely, the MBMM+ program also targets sleep hygiene and mood to further support regular physical activity engagement. Over the years of working with pregnant women, we have observed that once women notice how their regular physical activity helps their mood and sleep patterns they are often more likely to continue engaging in regular physical activity. During the first four weeks of the MBMM+ program, participants will receive electronic informational handouts covering topics on weight management (content will be based in part on Co-I Downs' Healthy Mom Zone intervention such as informing on benefits and guidelines of healthy GWG, tips on healthy eating, energy balance, and sleep quality) as well as the benefits and safety concerns related to prenatal physical activity. Starting week 5 of the 12-week intervention, participants will attend two in-person, group physical activity sessions per week with each session lasting approximately 60 minutes and will be held at a local community center located close to the recruitment clinics. Sessions will be held on weekday evenings and weekend mornings as these times were preferred by pregnant women. Given that pregnant women often express a lack of knowledge about safe physical activities during pregnancy, preventing them from engaging in physical activity, each session will include both didactic and experiential components to increase knowledge and skill building. Sessions will begin with a didactic component covering overcoming barriers to physical activity, goal setting, self-monitoring, problem solving, topics related to mood (stress management, family/work balance, wellness wheel), sleep hygiene (setting routines, avoiding stimulants, environmental supports), and additional physical activity topics (e.g., managing physical activity in postpartum, overcoming relapses). Participants will be given educational materials in print and electronic form based on their preferences. The experiential component (i.e., physical activity) will be 30 minutes in duration and involve primarily walking, at a moderate intensity, based on national recommendations coupled with yoga. Our formative work suggests that mothers prefer walking and find it more enjoyable in the form of groups. We have chosen to also include yoga to provide options for ways to be active that also positively impact sleep and mood and pregnant women report desiring prenatal yoga. All walking sessions will be facilitated by the peer leaders. The yoga sessions will be taught by an experienced prenatal yoga instructor residing in Denver, CO. Each session will have 3-4 peer leaders to help facilitate and model the physical activity component (i.e., will accompany women during their walking and yoga sessions to provide support and ensure safety (e.g., correct postures during yoga, monitoring exercise intensity and symptoms during walking sessions). Our MBMM formative work and expertise in community-based physical activity interventions suggests participants prefer peer group leaders because they foster a sense of community and social support within the group setting. Peer leaders will be compensated for their time working with the MBMM+ program and will be peer mothers from the community who are recent mothers (\< two years postpartum) who successfully engaged in regular physical activity during a previous pregnancy. Peer leaders will be identified by our research team, recreation center directors, and health care provider partners. At the end of every session, participants will check in with an assigned peer leader to discuss in small groups their weekly logs. Peer leaders will note the discussions that occurred amongst the participants in their group, describe barriers that were identified, problem-solving strategies that were suggested and used, and future goals/recommended action steps. This group work will help participants to learn ways to fit physical activity into their lifestyle and overcome barriers by receiving feedback from their peer leader and other group members. It will also ensure that the intervention is conducted and received in the way intended as the peer leaders and program manager/PI will review these small group progress notes each week and monitor intervention delivery. Peer leader training and fidelity: Weekly, the research team (PI/program manager) will have phone calls and/or in-person meetings with the group peer leaders to debrief and address any issues that may arise. The program manager and/or PI will be on-site for all sessions to ensure quality control of intervention delivery and data collection efforts by peer leaders. The PI will conduct a training session before the onset of the intervention with the peer group leaders to cover topics including how to engage in safe and effective physical activity during pregnancy, an overview of behavioral change theory and the behavioral skills that the intervention is targeting, ways to garner social support and leadership skills. The PI has been extensively trained by the Cooper Institute in Prenatal-Postnatal Physical Activity. The yoga instructor will have been extensively trained in prenatal yoga. Control Group: Women randomized to the control group will complete a similarly structured 12-week program; electronic materials related to various prenatal topics including preparation for birth, birthing options, and responsive parenting will be distributed twice a week for the first 4-weeks of the program. Starting week 5 of the 12-week intervention, participants will attend two in-person, group sessions per week with each session lasting approximately 60 minutes and will be held at a local community center located close to the recruitment clinics. Sessions will be held on weekday evenings and weekend mornings as these times were preferred by pregnant women.

Interventions

OTHERMy Baby My Move +

This is a community-based, peer-led 12-week wellness intervention to decrease excessive gestational weight gain.

OTHERControl

This is a 12-week basic prenatal education class.

Sponsors

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Randomized controlled trial (control and intervention)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 46 Years
Healthy volunteers
No

Inclusion criteria

* English-speaking * pregnant (6-10 weeks) women * aged 18-46 years * reside in Denver, CO * currently engaging in less than 120 minutes of moderate-intensity exercise per week * have medical clearance to exercise during pregnancy.

Exclusion criteria

-having conditions that preclude exercise (i.e. HCP has restricted patient from engaging in exercise according to AGOG's absolute contraindications to exercise (e.g. haemodynamically significant heart disease, restrictive lung disease, incompetent cervix/cerclage, persistent second or third trimester bleeding, placenta previa after 26 weeks gestation, premature labor during the current pregnancy, ruptured membranes, and pregnancy induced hypertension)

Design outcomes

Primary

MeasureTime frameDescription
Weight12 week post-baselineAverage weight

Secondary

MeasureTime frameDescription
Depression12 weeks post-baselineEdinburgh Postnatal Depression Scale (EPDS); scale: 1-30 with higher score indicating higher depression
Anxiety12 weeks post baselineGeneral Anxiety Disorder- 7 scale (GAD-7); 1-7 scale with higher score indicating higher anxiety
Physical Activity12 weeks Post-baselineThe Godin-Shephard Leisure-Time Physical Activity Questionnaire (LTEQ) assesses when someone engages in mild, moderate, and vigorous exercise for more than 15 minutes within one week. The leisure activity score is calculated using the following formula: leisure activity score = (9 x strenuous activity per week) + (5 x moderate activity per week) + (3 x light activity per week). Strenuous exercise is defined as heart beating rapidly, moderate exercise is defined as not exhausting, and light activity is described as minimal effort. Scores of 14 or less indicate insufficiently active/sedentary, scores of 14-23 indicate moderately active, and scores of more than 24 indicate active.

Countries

United States

Participant flow

Pre-assignment details

68 participants were consented - 18 dropped out prior to randomization due to physician request, no longer interested A total of 50 participants were randomized of which 49 completed all assessments.

Participants by arm

ArmCount
Intervention
During the first four weeks of the MBMM+ program, participants will receive electronic informational handouts covering topics on weight management as well as the benefits and safety concerns related to prenatal physical activity. Starting week 5 of the 12-week intervention, participants will attend two in-person, group physical activity sessions per week with each session lasting approximately 60 minutes and will be held at a local community center located close to the recruitment clinics. Sessions will be held on weekday evenings and weekend mornings as these times were preferred by pregnant women. Each session will include both didactic and experiential components to increase knowledge and skill building. Please note that in-person sessions were moved to online platform for the entire trial due to covid. My Baby My Move +: This is a community-based, peer-led 12-week wellness intervention to decrease excessive gestational weight gain.
25
Control
Electronic materials related to various prenatal topics including preparation for birth, birthing options, and responsive parenting will be distributed twice a week for the first 4-weeks of the program. Starting week 5 of the 12-week intervention, participants will attend two in-person, group sessions per week with each session lasting approximately 60 minutes and will be held at a local community center located close to the recruitment clinics. Control: This is a 12-week basic prenatal education class. Please note that in-person sessions were moved to online platform for the entire trial due to covid.
24
Total49

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyAdverse Event10

Baseline characteristics

CharacteristicInterventionControlTotal
Age, Continuous32.1 years
STANDARD_DEVIATION 4.87
31.5 years
STANDARD_DEVIATION 4.3
31.8 years
STANDARD_DEVIATION 4.5
Race/Ethnicity, Customized
Hispanic or Latino
7 participants4 participants11 participants
Race/Ethnicity, Customized
nonHispanic
18 participants20 participants38 participants
Region of Enrollment
United States
25 participants24 participants49 participants
Sex: Female, Male
Female
25 Participants24 Participants49 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants
Weight
Normal Weight
11 Participants15 Participants26 Participants
Weight
Obese
4 Participants4 Participants8 Participants
Weight
Overweight
8 Participants3 Participants11 Participants
Weight
Underweight
2 Participants2 Participants4 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 260 / 24
other
Total, other adverse events
0 / 260 / 24
serious
Total, serious adverse events
1 / 250 / 24

Outcome results

Primary

Weight

Average weight

Time frame: 12 week post-baseline

Population: Average Weight of pregnant women for intervention versus control at 12 weeks post-baseline

ArmMeasureValue (MEAN)Dispersion
InterventionWeight162.9 poundsStandard Deviation 29.9
ControlWeight162.3 poundsStandard Deviation 37.6
Secondary

Anxiety

General Anxiety Disorder- 7 scale (GAD-7); 1-7 scale with higher score indicating higher anxiety

Time frame: 12 weeks post baseline

Population: 12 wk post-baseline anxiety scores for intervention and control

ArmMeasureValue (MEAN)Dispersion
InterventionAnxiety4.7 units on a scaleStandard Deviation 3.1
ControlAnxiety3.7 units on a scaleStandard Deviation 3.2
Secondary

Depression

Edinburgh Postnatal Depression Scale (EPDS); scale: 1-30 with higher score indicating higher depression

Time frame: 12 weeks post-baseline

Population: Depression scores at 12 wks post baseline for intervention vs control

ArmMeasureValue (MEAN)Dispersion
InterventionDepression8.1 units on a scaleStandard Deviation 5.4
ControlDepression6.3 units on a scaleStandard Deviation 4.4
Secondary

Physical Activity

The Godin-Shephard Leisure-Time Physical Activity Questionnaire (LTEQ) assesses when someone engages in mild, moderate, and vigorous exercise for more than 15 minutes within one week. The leisure activity score is calculated using the following formula: leisure activity score = (9 x strenuous activity per week) + (5 x moderate activity per week) + (3 x light activity per week). Strenuous exercise is defined as heart beating rapidly, moderate exercise is defined as not exhausting, and light activity is described as minimal effort. Scores of 14 or less indicate insufficiently active/sedentary, scores of 14-23 indicate moderately active, and scores of more than 24 indicate active.

Time frame: 12 weeks Post-baseline

Population: 12 weeks post-baseline assessment of physical activity for intervention and control.

ArmMeasureValue (MEAN)Dispersion
InterventionPhysical Activity48.0 units on a scaleStandard Deviation 17.8
ControlPhysical Activity35.9 units on a scaleStandard Deviation 9.11

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026