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EQ-PREMOTE

Equity in Remote Pregnancy Care: Developing Digital Solutions for Women in Vulnerable Circumstances - EQ-PREMOTE

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57598
Enrollment
15
Registered
2025-04-16
Start date
2025-09-01
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Vulnerable circumstances during pregnancy and remote pregnancy care

Interventions

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria:  All: Informed consent is needed to participate. Age = 18 years (Recently) Pregnant womenWomen who are currently pregnant, with a pregnancy duration between 12 and 30 weeks (30 weeks is the maximum to allow for multiple consecutive meetings before childbirth), OR women who have given birth within the past year, ANDWomen living in vulnerable circumstances, defined by one or more of the following factors:Living without a partnerHaving a low family incomeBelonging to a non-Dutch cultural background(Note: A non-Dutch cultural background alone is not considered a criterion for vulnerability. However, we aim to include individuals from non-Dutch cultural backgrounds who may face challenges related to language barriers, cultural differences, and integration into Dutch society, while also valuing diverse perspectives.)Having low health literacyA healthcare professional may also assess a pregnant woman as vulnerable based on a comprehensive evaluation of her personal, medical, and social circumstances.Maternal and Child Healthcare and -social care professionalsAffinity with vulnerable pregnant groups Affinity with RDPC  

Exclusion criteria

Exclusion criteria:  Absence of Dutch language skills 

Design outcomes

Primary

MeasureTime frame
The main project endpoint is a tailored care pathway for RDPC for pregnant women in vulnerable circumstances. The scientific endpoint is the documentation of needs and preferences for a successful care pathway for this group.

Secondary

MeasureTime frame
The evaluation of the co-creation process and result, encompassing co-creators’ opinions, satisfaction and contributions (e.g. measured through attendance rates, questionnaires, and interviews).

Countries

Netherlands

Contacts

Public ContactR. Vellekoop - van Ravenswaaij

Erasmus MC, Universitair Medisch Centrum Rotterdam

r.vellekoop-vanravenswaaij@erasmusmc.nl010-7040704

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jun 21, 2026