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Healthy for Two-Home Visiting (H42-HV): Health Coaching for Pregnant Women

Primary Purpose

Postpartum Weight Retention, Pregnancy Weight Gain, Overweight and Obesity

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Healthy for Two-Health Coaching (H42)
Maintain Healthy in Pregnancy and Postpartum(mHIPP)
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Postpartum Weight Retention focused on measuring Behavioral Intervention, Early Childhood Home Visiting, Overweight, Obesity, Postpartum, Pregnancy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Pregnant, ≤33 weeks gestation Singleton pregnancy Pre pregnancy BMI≥25.0 Kg/m^2 (calculated based on self-reported pre pregnancy height and weight) Able to provide informed consent English or Spanish speaking Enrolled in participating home visiting program Completion of screening and baseline data collection Willing to participate in the intervention and data collection procedure (e.g., home weights) Exclusion Criteria: Type 1 diabetes or taking insulin prior to delivery > 33 weeks gestation Pregnant with multiple fetuses Unable to walk 1 block without pain or shortness of breath Not cleared by the study's clinicians or home visiting program staff Planning to relocate from area during next 1 year Active substance abuse disorder (except marijuana) Psychiatric or substance use related hospitalization in past 1 year Active eating disorder

Sites / Locations

  • Johns Hopkins School of NursingRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Healthy for Two-Health Coaching (H42)

Maintain Health in Pregnancy and Postpartum (mHIPP)

Arm Description

Those assigned to the intervention group will receive the 8 to 11 month H42 health coaching intervention in addition to usual home visiting and usual prenatal and postpartum care clinical services. Intervention duration will depend on the participant's gestational age at the of enrollment. Participants can be enrolled as early in pregnancy as 20 weeks gestation and as late as 33 weeks gestation. All participants would be enrolled for 6 months postpartum. Therefore, the minimum time in the intervention would be 8 months and maximum would be 11 months.

Those assigned to the "usual home visiting plus" comparison group, called maintain health in pregnancy and postpartum (mHIPP), will receive the typical, evidence-based experience in participants' home visiting program in addition to the participants' usual prenatal and postpartum care clinical services. In addition, the investigators will provide a brief (less than 5 minutes) maternal warning signs educational video that is available in English or Spanish. The video was developed for a home visiting client audience and is publicly available, https://mdmom.org/warningsigns.

Outcomes

Primary Outcome Measures

Change in postpartum weight (retention)
Difference between pre-pregnancy weight and weight at 6 months postpartum. Pre-pregnancy weight (baseline) will be self-reported and then confirmed by prenatal clinic medical records. 6 month postpartum weight will be obtained via BodyTrace study scales provided to all participants.

Secondary Outcome Measures

Change in gestational weight (gain)
Difference between pre-pregnancy weight and delivery weight. Pre-pregnancy weight will be self-reported and then confirmed by prenatal clinic records. Delivery weight will be obtained via BodyTrace study scales provided to each participant.
Change in maternal diet as assessed by the Dietary Screener Questionnaire (DSQ)
Dietary intake will be assessed using the NHANES 2009-10 Dietary Screener Questionnaire (DSQ) Eating Habits Questionnaire (28-items). Scoring equations exist to estimate daily intake of fruits/vegetables, dairy, added sugars, whole grains, and calcium.
Change in maternal physical activity as assessed by the International Physical Activity Questionnaire (IPAQ)
The Short Form International Physical Activity Questionnaire contains 9 items to collect data on health-related physical activity in the past seven days. Physical activity is categorized as high (at least one hour of moderate intensity exercise daily), moderate (approximately 30 minutes of moderate intensity exercise most days), or low (not meeting the criteria of high or moderate exercise).
Maternal smoking habits as assessed by the Center for Disease Control and Prevention Pregnancy Risk Assessment Monitoring System (CDC PRAMS)
A four-item portion of the PRAMS survey will be utilized to determine cigarette use before and during pregnancy.
Change in breastfeeding Practice as assessed by the Center for Disease Control and Prevention Infant Feeding Practices Survey (CDC IFPS)
A 4-item portion of the CDC IFPS will be used at 2,4, and 6 months postpartum to assess current breastfeeding practice.
Breastfeeding Intention as assessed by the Center for Disease Control and Prevention Infant Feeding Practices Survey (CDC IFPS)
A two-item portion of the CDC IFPS will be used to assess breastfeeding intention.
Change in maternal depression as assessed by the Edinburgh Postpartum Depression scale
The Edinburgh Postpartum Depression scale is a 10-item measure assessing changes in mood over the past seven days. The last question related to suicidal ideation has been removed. Mothers who score above 13 are likely to be suffering from a depressive illness of varying severity.
Change in maternal sleep habits as assessed by the Pittsburgh Sleep Quality Index (PSQI)
The PSQI is a 19-item questionnaire assessing sleep habits in the past seven days. Nineteen individual items generate seven "component" scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. The sum of scores for these seven components yields one global score (0-21) and higher scores indicate worse sleep quality.
Change in maternal social support as assessed by the Functional Social Support Questionnaire (FSSQ)
The FSSQ is an 8-item measure that evaluates confidant support and affective support. Responses are scored 1-5 and an average is calculated based on the response from all eight items. A higher score indicates greater perceived social support.
Maternal healthcare utilization as assessed by Medicaid data extraction
Postpartum OBGYN visit and primary care provider visit by six months.
Infant healthcare utilization as assessed by Medicaid data extraction
Well-child visit appointments through six months of life.

Full Information

First Posted
November 9, 2022
Last Updated
July 19, 2023
Sponsor
Johns Hopkins University
Collaborators
National Institute on Minority Health and Health Disparities (NIMHD)
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1. Study Identification

Unique Protocol Identification Number
NCT05619705
Brief Title
Healthy for Two-Home Visiting (H42-HV): Health Coaching for Pregnant Women
Official Title
Effectiveness of Health Coaching to Reduce Cardiometabolic Risk in Early Home Visiting Services
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 25, 2023 (Actual)
Primary Completion Date
June 30, 2025 (Anticipated)
Study Completion Date
August 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
National Institute on Minority Health and Health Disparities (NIMHD)

4. Oversight

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

5. Study Description

Brief Summary
The purpose of this study is to compare the effectiveness of H42-HV integrated into home visiting compared with usual home visiting services in reducing postpartum weight retention (difference between pre-pregnancy weight and weight at 6 months postpartum) among pregnant and postpartum people. The intervention is tailored for Black and Latinx pregnant and postpartum people and, ultimately, aims to address inequities in cardiometabolic health.
Detailed Description
There are four components of the H42-HV intervention: 1) Health coaching calls; 2) H42 web-based app for learning activities and goal setting functions; 3) Tracking of health behaviors (diet, exercise), and 4) Self-weighing (weekly). The overarching behavioral goals of the intervention are for participants to have lower postpartum weight retention at 6 months after delivery. Weight and behavioral goals will be promoted through the COACH Plan, a behavioral model guiding coaching calls, behavioral tracking targets and learning activities. Coaches will refer to home visitors for additional support and community resources, based on an established protocol. Telephone health coaching calls by trained health coaches. Calls start at enrollment, between 20-33-weeks gestation through 6 months postpartum. Although coaching calls will occur by phone or Zoom (~20 mins), when possible, some coach contact could occur at the time of home visits in person. Online interactive learning activities. Literacy adaptation ensured Learning Activities are at <5th grade reading level. All activities are translated into Spanish and culturally adapted to create a parallel program. Online learning activities contain embedded images (people and settings) that reflect the diversity of the investigators' target population, examples of activities that are readily available in the community and maximize the use of white space, large text and simple graphics to enhance readability and accessibility of the educational content. The investigators enhanced the platform to enable an interactive goal-setting functionality for participants to set health goals paced with participants' Learning Activities and calls. The online program is maintained and monitored by the study's health coach managers. Health behavior tracking (diet and exercise). Participants will receive specific skill-building on how to track diet and exercise behaviors via mainstream mobile app or paper/pencil, using procedures from the investigators' current trial. Coaches will be able to discuss tracking data with participants. Mainstream tracking apps are available in both Spanish and English. Weekly self-weighing. Participants will be asked to weigh themselves weekly at home using the participants' study scale.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postpartum Weight Retention, Pregnancy Weight Gain, Overweight and Obesity, Behavior, Health
Keywords
Behavioral Intervention, Early Childhood Home Visiting, Overweight, Obesity, Postpartum, Pregnancy

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
The design of the study is a randomized, two parallel-arm clinical trial. The investigators will be applying principles of a hybrid type 1 effectiveness-implementation randomized control trial
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
360 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Healthy for Two-Health Coaching (H42)
Arm Type
Experimental
Arm Description
Those assigned to the intervention group will receive the 8 to 11 month H42 health coaching intervention in addition to usual home visiting and usual prenatal and postpartum care clinical services. Intervention duration will depend on the participant's gestational age at the of enrollment. Participants can be enrolled as early in pregnancy as 20 weeks gestation and as late as 33 weeks gestation. All participants would be enrolled for 6 months postpartum. Therefore, the minimum time in the intervention would be 8 months and maximum would be 11 months.
Arm Title
Maintain Health in Pregnancy and Postpartum (mHIPP)
Arm Type
Active Comparator
Arm Description
Those assigned to the "usual home visiting plus" comparison group, called maintain health in pregnancy and postpartum (mHIPP), will receive the typical, evidence-based experience in participants' home visiting program in addition to the participants' usual prenatal and postpartum care clinical services. In addition, the investigators will provide a brief (less than 5 minutes) maternal warning signs educational video that is available in English or Spanish. The video was developed for a home visiting client audience and is publicly available, https://mdmom.org/warningsigns.
Intervention Type
Behavioral
Intervention Name(s)
Healthy for Two-Health Coaching (H42)
Intervention Description
The H42-HV intervention includes health coaching calls, H42 web based app, mobile phone-based tracking.
Intervention Type
Behavioral
Intervention Name(s)
Maintain Healthy in Pregnancy and Postpartum(mHIPP)
Other Intervention Name(s)
"Usual Home Visiting Plus"
Intervention Description
A brief video on maternal warning signs that is available in English or Spanish.
Primary Outcome Measure Information:
Title
Change in postpartum weight (retention)
Description
Difference between pre-pregnancy weight and weight at 6 months postpartum. Pre-pregnancy weight (baseline) will be self-reported and then confirmed by prenatal clinic medical records. 6 month postpartum weight will be obtained via BodyTrace study scales provided to all participants.
Time Frame
Baseline and 6 months postpartum
Secondary Outcome Measure Information:
Title
Change in gestational weight (gain)
Description
Difference between pre-pregnancy weight and delivery weight. Pre-pregnancy weight will be self-reported and then confirmed by prenatal clinic records. Delivery weight will be obtained via BodyTrace study scales provided to each participant.
Time Frame
Baseline and immediately before delivery
Title
Change in maternal diet as assessed by the Dietary Screener Questionnaire (DSQ)
Description
Dietary intake will be assessed using the NHANES 2009-10 Dietary Screener Questionnaire (DSQ) Eating Habits Questionnaire (28-items). Scoring equations exist to estimate daily intake of fruits/vegetables, dairy, added sugars, whole grains, and calcium.
Time Frame
Baseline, 37 weeks gestation, 2 months postpartum, 4 months postpartum, 6 months postpartum
Title
Change in maternal physical activity as assessed by the International Physical Activity Questionnaire (IPAQ)
Description
The Short Form International Physical Activity Questionnaire contains 9 items to collect data on health-related physical activity in the past seven days. Physical activity is categorized as high (at least one hour of moderate intensity exercise daily), moderate (approximately 30 minutes of moderate intensity exercise most days), or low (not meeting the criteria of high or moderate exercise).
Time Frame
Baseline, 37 weeks gestation, 2 months postpartum, 4 months postpartum, 6 months postpartum
Title
Maternal smoking habits as assessed by the Center for Disease Control and Prevention Pregnancy Risk Assessment Monitoring System (CDC PRAMS)
Description
A four-item portion of the PRAMS survey will be utilized to determine cigarette use before and during pregnancy.
Time Frame
Baseline
Title
Change in breastfeeding Practice as assessed by the Center for Disease Control and Prevention Infant Feeding Practices Survey (CDC IFPS)
Description
A 4-item portion of the CDC IFPS will be used at 2,4, and 6 months postpartum to assess current breastfeeding practice.
Time Frame
2 months postpartum, 4 months postpartum, 6 months postpartum
Title
Breastfeeding Intention as assessed by the Center for Disease Control and Prevention Infant Feeding Practices Survey (CDC IFPS)
Description
A two-item portion of the CDC IFPS will be used to assess breastfeeding intention.
Time Frame
37 weeks gestation
Title
Change in maternal depression as assessed by the Edinburgh Postpartum Depression scale
Description
The Edinburgh Postpartum Depression scale is a 10-item measure assessing changes in mood over the past seven days. The last question related to suicidal ideation has been removed. Mothers who score above 13 are likely to be suffering from a depressive illness of varying severity.
Time Frame
Baseline, 37 weeks gestation, 2 months postpartum, 4 months postpartum, 6 months postpartum
Title
Change in maternal sleep habits as assessed by the Pittsburgh Sleep Quality Index (PSQI)
Description
The PSQI is a 19-item questionnaire assessing sleep habits in the past seven days. Nineteen individual items generate seven "component" scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. The sum of scores for these seven components yields one global score (0-21) and higher scores indicate worse sleep quality.
Time Frame
Baseline, 2 months postpartum, 4 months postpartum, 6 months postpartum
Title
Change in maternal social support as assessed by the Functional Social Support Questionnaire (FSSQ)
Description
The FSSQ is an 8-item measure that evaluates confidant support and affective support. Responses are scored 1-5 and an average is calculated based on the response from all eight items. A higher score indicates greater perceived social support.
Time Frame
Baseline, 36-38 weeks prenatal, 2 months postpartum, 4 months postpartum, 6 months postpartum
Title
Maternal healthcare utilization as assessed by Medicaid data extraction
Description
Postpartum OBGYN visit and primary care provider visit by six months.
Time Frame
Up to 6 months after delivery
Title
Infant healthcare utilization as assessed by Medicaid data extraction
Description
Well-child visit appointments through six months of life.
Time Frame
Up to 6 months after delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnant, ≤33 weeks gestation Singleton pregnancy Pre pregnancy BMI≥25.0 Kg/m^2 (calculated based on self-reported pre pregnancy height and weight) Able to provide informed consent English or Spanish speaking Enrolled in participating home visiting program Completion of screening and baseline data collection Willing to participate in the intervention and data collection procedure (e.g., home weights) Exclusion Criteria: Type 1 diabetes or taking insulin prior to delivery > 33 weeks gestation Pregnant with multiple fetuses Unable to walk 1 block without pain or shortness of breath Not cleared by the study's clinicians or home visiting program staff Planning to relocate from area during next 1 year Active substance abuse disorder (except marijuana) Psychiatric or substance use related hospitalization in past 1 year Active eating disorder
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kelly M Bower, PhD, MSN/MPH
Phone
410-955-4280
Email
kbower1@jhu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Wendy Bennett, MD,MPH
Phone
410-502-6081
Email
wendy.bennett@jhmi.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kelly Bower, PhD, MSN/MPH
Organizational Affiliation
Johns Hopkins School of Nursing
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wendy Bennett, MD,MPH
Organizational Affiliation
Johns Hopkins School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins School of Nursing
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21205
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Becka Richman, MSN/MPH
Phone
443-931-5082
Email
rrichma1@jh.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Healthy for Two-Home Visiting (H42-HV): Health Coaching for Pregnant Women

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