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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05365828
Other study ID # EDGE 124858
Secondary ID IRAS 264198
Status Recruiting
Phase
First received
Last updated
Start date May 17, 2022
Est. completion date March 2024

Study information

Verified date May 2023
Source University College, London
Contact Study Coordinator
Phone +44 020 3108 4358
Email stnvkll@ucl.ac.uk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pregnancy care typically assumes patients are heterosexual married women whose gender matches their assigned sex (i.e., cisgender), stigmatizing patients and creating limitations, blocking affirming care. Consequently, lesbian, gay, bisexual, queer, intersex, asexual, and/or transgender (LGBTQIA+) parents face minority stress as discrimination in antenatal care. This mixed-methods study assesses stressors and resilience factors on pregnancy and birth outcomes. LGBTQIA+ pregnant parents (n=200) are case-matched with cisheterosexual peers (n=600). Primary data comes from two panel surveys, one antenatally and one postpartum, combined with medical records. A sub-sample (n=30) will complete a journal between surveys. Findings will inform care guidelines and provider training.


Description:

Patients using reproductive health services, like care during pregnancy (called antenatal care), are most often assumed to be heterosexual married women whose gender matched their sex assigned at birth (i.e., cisgender). Due to these assumptions, pregnancy care procedures are based on a sweeping assumption of who becomes pregnant and gives birth. This assumption is based on the pregnant person's gender and/or sexual orientation. As a result of this assumption, parents who are lesbian, gay, bisexual, queer, intersex, asexual, non-binary, and/or transgender (LGBTQIA+) can experience stress in the form of stigma, prejudice, and discrimination (i.e. "minority stress"). In the United Kingdom, there are 525,000 LGBTQIA+ potential gestational patients who may face this type of stress while receiving pregnancy care. That means that there is a preventable higher risk for pregnancy and birth complications caused by increased stress during pregnancy and daily life. These complications include macrosomia, pre-term birth, and low-birth weight. Preventable stress, also called minority stress, links to this increase in health problems outside of pregnancy as well. Since minority stress influences patient/parents' health, it is also called a risk or vulnerability. Resilience, or the ability to overcome stress and discrimination, can sometimes help improve health outcomes. However, little is known about which types of resilience can be helpful for LGBTQIA+ parents given their unique experiences of minority stress. The planned observational study will investigate the ways in which experiences of minority stress and resilience in pregnancy care are associated with parent health and birth outcomes. A sample of pregnant patients (N=800) from maternity wards in and around London will take part through an online panel survey (completed twice) that will be linked to each patient/participant's electronic health records to create a quantitative dataset. Participant recruitment will focus on LGBTQIA+ pregnant patients (n=200). A matched comparison sample of cisgender, heterosexual pregnant patients (n=600) will also be recruited to take part from the same maternity. From the full sample, patient/parents from University College London Hospital will be invited to complete an at-home journal activity which will provide qualitative data on their experiences of minority stress and resilience. This smaller group (n=30). Results from this study can be used to inform LGBTQIA+ guidelines, training, and help make reproductive healthcare more inclusive.


Recruitment information / eligibility

Status Recruiting
Enrollment 800
Est. completion date March 2024
Est. primary completion date March 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 49 Years
Eligibility Inclusion Criteria: - Legal adult of reproductive age (18-49) - Identifies as a lesbian, gay, bisexual, queer, nonbinary, intersex, and/or transgender (or cisgender and heterosexual for comparison sample) - Currently pregnant and receiving antenatal care at one of the study sites Exclusion Criteria: - Any pregnant persons under the age of 18 - Pregnant individuals using sites locations for Urgent care, A&E, non-antenatal services only

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom King's College Hospital NHS Foundation Trust Brixton
United Kingdom Kingston Hospital NHS Foundation Trust Kingston Upon Thames
United Kingdom Barts Health NHS Trust London
United Kingdom Guy's and St Thomas' NHS Foundation Trust London
United Kingdom Homerton University Hospital NHS Foundation Trust London
United Kingdom Imperial College Healthcare NHS Trust London
United Kingdom Lewisham and Greenwich NHS Trust London
United Kingdom Royal Free London NHS Foundation Trust London
United Kingdom St George's University Hospitals NHS foundation Trust London
United Kingdom University College London Hospital NHS Foundation Trust London
United Kingdom Whittington Health NHS Trust London
United Kingdom Epsom and St Helier University Hospitals NHS Trust Sutton
United Kingdom West Hertfordshire Teaching Hospitals NHS Trust Watford
United Kingdom University Hospitals Sussex NHS Foundation Worthing

Sponsors (17)

Lead Sponsor Collaborator
University College, London Barts & The London NHS Trust, Economic and Social Research Council, United Kingdom, Epsom and St Helier University Hospitals NHS Trust, Guy's and St Thomas' NHS Foundation Trust, Homerton University Hospital, Imperial College Healthcare NHS Trust, King's College Hospital NHS Trust, Kingston Hospital NHS Trust, Lewisham and Greenwich NHS Trust, Royal Free Hospital NHS Foundation Trust, St George's University Hospital NHS Foundation Trust, The Whittington Hospital NHS Trust, UCL, Bloomsbury and East London (UBEL) Doctoral Training Partnership, University College London Hospitals, University Hospitals Sussex NHS Foundation, West Hertfordshire Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Primary Scientific Aim - Parental Health The outcome measured for impact from resilience and vulnerability is parent health as allostatic load (as health data from routine antenatal check-ups). Scales will be composited into intrapersonal stressors (i.e., felt stigma, level of outness), interpersonal stressors (i.e., homelessness & child welfare, stressful life events/stress, everyday discrimination, chronic strains, police interactions), structural stressors (i.e., household social vulnerability index, deprivation score), intrapersonal resilience (i.e., coping, social support), interpersonal resilience (i.e., patient experience scale, shared decision-making, emotional reactivity), and structural resilience (i.e., community connectedness, civic engagement). through study completion, up to 10 months
Primary Primary Scientific Aim - Infant Health The composite for parent health (i.e. allostatic load from Outcome 1) will be assessed to see if there is an impact on infant health (a composite of head circumference, gestational length, birth weight, birth length, Apgar score). through study completion, up to 10 months
Secondary Secondary Scientific Aim - Understanding additional stressors and resilience Qualitative journals will be used to assess for additional stressors and resilience resources to ascertain if there are measures that have not been accounted for within the quantitative measures. These are presently unknown, as the point of the measure is to uncover these dimensions of the constructs of resilience and vulnerability. through study completion, up to 10 months
Secondary Secondary Scientific Aim - Contextualising resilience and vulnerability The same qualitative journals in outcome 3 will also provided narratives about the experiences of parents with extreme resilience and vulnerability scores. The assessment of these narratives will be done to help contextualise the presence of extreme scores for parents receiving antenatal care at UCLH. The contents of these narratives collectively will be reported within the final findings alongside the quantitative data, as well as will be quoted specifically when relevant. through study completion, up to 10 months
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