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Mom♥Health2.0 for Cardiovascular Health in Mothers

This study is testing a program called Mom♥Health2.0 to help mothers improve their heart health. It's designed for mothers aged 18-49 who are primary caregivers of young children (5 years old or younger) attending formal childcare, and who speak English or Spanish. The Mom♥Health2.0 program involves 10 weeks of individual phone calls for education and counseling on healthy living and stress reduction, plus two in-person sessions at childcare centers. Researchers want to see if the program is practical to run (feasibility), if mothers like it (acceptability), and its early effects. They plan to enroll 50 mothers from childcare centers in New York City. The current status of this study is unclear.

Study design
This is an interventional study, meaning participants will receive a specific program. It aims to enroll 50 mothers.
What's involved
You would participate in a 10-week program, including 8 weekly phone calls and two in-person sessions.
Compensation
Not stated in the trial record.
Follow-up
Your participation will be tracked for up to 18 weeks (end of study).

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07724821

Community Engagement for Cardiovascular Health Promotion in Mothers (MomHeartHealth2.0)

Not Yet Recruiting
NAAges 18–49InterventionalSupportive care
NYU Langone Health
~50 participants
Updated 2026-07-24 on ClinicalTrials.gov
What's tested:Mom♥Health2.0

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Feasibility: Program Completion
Measured over Up to Week 10 (End of Intervention)
+3 more outcomes measured

Conditions

Cardiovascular Health

Explore related trials

Cardiovascular Health

Where it's being run

1 sites across 1 states
New York1

Study leadership

  • Milla Arabadjian, PhD · PRINCIPAL_INVESTIGATOR · NYU Langone Health

Who to contact

Milla Arabadjian, PhD
[email protected]
516-663-1668
Email the study team

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Female adults, age 18-49 years.
Mothers, self-identified as primary caregivers of children ≤ 5 years (biological, adopted, fostered) whose child(ren) attend formal childcare (no home daycare);
English or Spanish speaking.
Willing and able to consent to participation.

Exclusion

Significant cognitive impairment (evident during screening)
Current participation in another behavioral clinical trial

What this trial measures

  • Feasibility: Program CompletionUp to Week 10 (End of Intervention)

    Feasibility is measured as the number of participants with 80% participant program completion.

  • Feasibility: Appointment SchedulingUp to Week 18 (End of Study)

    Feasibility is measured as the number of participants with 80% clinic/social services appointment scheduled for identified needs

  • Acceptability: Consent RateBaseline

    Acceptability is measured as the consent rate of eligible mothers; the aim is 80%.

  • Acceptability: Client SatisfactionWeek 18 (End of Study)

    Acceptability is measured as the number of participants with an average post-intervention Client Satisfaction Questionnaire-8 score ≥ 25. The questionnaire comprises 8-items and assesses program satisfaction in: quality, whether it has met individual needs, if the individual would recommend to others. The total range is 8-32; a score of 25 is an established cutoff for good satisfaction.