The Midlands and North of England Stillbirth Study

NCT ID: NCT02025530

Last Updated: 2019-10-11

Study Results

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1030 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-04-01

Study Completion Date

2017-12-31

Brief Summary

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The United Kingdom has one of the highest rates of stillbirth in Europe, with more than 4,000 stillbirths every year; which equates to more than 11 deaths every day. Furthermore, this rate has changed very little over the last 20 years. This loss of life and the adverse psychological consequences urgently needs addressing.

A recent New Zealand study investigating modifiable factors associated with stillbirth (the Auckland Stillbirth Study) found that mothers who did not go to sleep on their left side had a twofold risk of late stillbirth (≥28 weeks gestation) compared to mothers who did go to sleep on their left side. These novel findings need urgent confirmation.

This proposed study aims to confirm or refute these findings and to ascertain whether a preventative programme should be introduced. This proposed study aims to confirm or refute the findings of the Auckland Stillbirth Study.

Participants will be recruited from maternity units in the Midlands and North of England (led by centres in Liverpool, Manchester, West Yorkshire and Birmingham). 291 women with a singleton late stillbirth without congenital abnormality will be interviewed by research midwives shortly after the birth. A control group of 580 women with ongoing pregnancies will be interviewed at a gestation group matched to that at which stillbirths occurred. These data will determine whether an intervention study should be considered. If there is a causal relationship between maternal sleep position and late stillbirth we estimate that upto 37% of late stillbirths might be prevented.

Detailed Description

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The death of an unborn child is a prevalent and tragic public health problem which currently affects millions of families worldwide. Late stillbirth (at or beyond 28 weeks of gestation) is one of the few potentially avoidable maternal and child health problems where the rate of decline in high income countries has slowed in recent decades \[1\]. The United Kingdom currently has one of the highest rates of stillbirth in Europe, ranking 33rd out of 35 high income countries.

The variations in stillbirth rates between high income countries suggest that it should be possible to make further reductions in late stillbirths. The estimated annual reduction in rates of late stillbirth over recent decades is about 1.1% \[1\], compared to 2.1% for neonatal death rates, with a resultant increase in the proportion of perinatal deaths (stillbirths plus neonatal deaths) attributable to stillbirth \[2\]. The Lancet Stillbirth Series \[1, 3, 4\] has highlighted the silent but prevalent public health problem of stillbirth and together with Sands and the Royal College Of Obstetricians and Gynaecologists has called for research to address these unacceptably high rates.

Current established risk factors for late stillbirth in high income countries include: advanced maternal age (\>35 years) \[5\], high pre-pregnancy body mass index (BMI) \[6\], smoking \[7\], reduced antenatal care attendance \[8\], low socioeconomic status \[8\] and small for gestational age (SGA) infants \[9\]. A meta-analysis of population based studies addressing risk factors for stillbirth found that the three most important modifiable risk factors were overweight and obesity (population attributable risk 818%) advanced maternal age (population attributable risk 68%), and smoking (population attributable risk 47%) \[3\]. Of these only, cigarette smoking may be realistically addressed after pregnancy has started. There has been limited research investigating the role of novel, modifiable factors which have the potential to advance knowledge and address the important gaps in the field of stillbirth research.

This study aims to explore modifiable risk factors for late stillbirth in the UK and to substantiate the recent identification of a new modifiable risk factor for unexpected late pregnancy stillbirths. In the Auckland Stillbirth Study \[10\] our New Zealand collaborators discovered an approximately two-fold increase in late stillbirth with non-left sided maternal sleep position on the night before the baby died. In addition, women who did not get up at night and those who slept during the day were also at increased risk of stillbirth. The strength of this primary finding was unanticipated and now maternal sleep position requires urgent, rigorous evaluation in another population. MiNESS aims to address these factors.

This multi-centered case control study will recruit 291 women who have experienced a late (≥28 weeks gestation) matched with 580 women who have a continuing pregnancy at the same gestation (controls). The women will be interviewed by an experienced research midwife and an in depth questionnaire will be completed.

Analysis will be carried out using the standard Mantel-Haenszel odds ratio analysis used in case-control studies. Unconditional logistic regression will be used to adjust for potential confounders and to determine the presence of interactions.

Conditions

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Stillbirth

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Cases

A structured questionnaire will be administered to women who have experienced a late ≥ 28 weeks gestation stillbirth, who have a singleton pregnancy with no congenital abnormality.

Questionnaire

Intervention Type OTHER

An indepth interview will be carried out and a structured questionnaire will be completed by both cases and controls

Controls

A structured questionnaire will be administered to controls. These are women matched to the case group by gestation and unit of birth, who have a normal ongoing singleton pregnancy with no congenital abnormality.

Questionnaire

Intervention Type OTHER

An indepth interview will be carried out and a structured questionnaire will be completed by both cases and controls

Interventions

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Questionnaire

An indepth interview will be carried out and a structured questionnaire will be completed by both cases and controls

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Women who experience a stillbirth ≥28 weeks gestation in a participating unit.


* Women with a normal pregnancy matched to gestation and unit of birth to the cases.

Exclusion Criteria

* Fetal death prior to 28 weeks gestation.
* Women who's babies have a significant congenital abnormality.
* Women with multiple pregnancy.
* Maternal age below 16 years.
* Women unable to give informed consent.


* Pregnancy under 28 weeks gestation.
* Women who's babies have a significant congenital abnormality.
* Women with multiple pregnancy.
* Maternal age below 16 years.
* Women unable to give informed consent.
Minimum Eligible Age

16 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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University of Manchester

OTHER

Sponsor Role lead

Responsible Party

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Dr Alexander Heazell

Senior Clinical Lecturer in Obstetrics

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Tomasina Stacey

Role: PRINCIPAL_INVESTIGATOR

Mid Yorkshire NHS Trust

Edwin Mitchell

Role: PRINCIPAL_INVESTIGATOR

University of Auckland, New Zealand

Lesley McCowan

Role: PRINCIPAL_INVESTIGATOR

University of Auckland, New Zealand

Bill Martin

Role: PRINCIPAL_INVESTIGATOR

Birmingham Women's Hospital NHS Foundation Trust

Devender Roberts

Role: PRINCIPAL_INVESTIGATOR

Liverpool Women's NHS Foundation Trust

Locations

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Liverpool Women's NHS Foundation Trust

Liverpool, Merseyside, United Kingdom

Site Status

Birmingham Women's Hospital NHS Foundation Trust

Birmingham, West Midlands, United Kingdom

Site Status

Mid Yorkshire NHS Trust

Dewsbury, Yorkshire, United Kingdom

Site Status

Central Manchester University Hospitals NHS Foundation Trust

Manchester, , United Kingdom

Site Status

Countries

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United Kingdom

References

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Cousens S, Blencowe H, Stanton C, Chou D, Ahmed S, Steinhardt L, Creanga AA, Tuncalp O, Balsara ZP, Gupta S, Say L, Lawn JE. National, regional, and worldwide estimates of stillbirth rates in 2009 with trends since 1995: a systematic analysis. Lancet. 2011 Apr 16;377(9774):1319-30. doi: 10.1016/S0140-6736(10)62310-0.

Reference Type BACKGROUND
PMID: 21496917 (View on PubMed)

Rajaratnam JK, Marcus JR, Flaxman AD, Wang H, Levin-Rector A, Dwyer L, Costa M, Lopez AD, Murray CJ. Neonatal, postneonatal, childhood, and under-5 mortality for 187 countries, 1970-2010: a systematic analysis of progress towards Millennium Development Goal 4. Lancet. 2010 Jun 5;375(9730):1988-2008. doi: 10.1016/S0140-6736(10)60703-9. Epub 2010 May 27.

Reference Type BACKGROUND
PMID: 20546887 (View on PubMed)

Flenady V, Koopmans L, Middleton P, Froen JF, Smith GC, Gibbons K, Coory M, Gordon A, Ellwood D, McIntyre HD, Fretts R, Ezzati M. Major risk factors for stillbirth in high-income countries: a systematic review and meta-analysis. Lancet. 2011 Apr 16;377(9774):1331-40. doi: 10.1016/S0140-6736(10)62233-7.

Reference Type BACKGROUND
PMID: 21496916 (View on PubMed)

Froen JF, Cacciatore J, McClure EM, Kuti O, Jokhio AH, Islam M, Shiffman J; Lancet's Stillbirths Series steering committee. Stillbirths: why they matter. Lancet. 2011 Apr 16;377(9774):1353-66. doi: 10.1016/S0140-6736(10)62232-5.

Reference Type BACKGROUND
PMID: 21496915 (View on PubMed)

Rasmussen S, Albrechtsen S, Irgens LM, Dalaker K, Maartmann-Moe H, Vlatkovic L, Markestad T. Risk factors for unexplained antepartum fetal death in Norway 1967-1998. Early Hum Dev. 2003 Feb;71(1):39-52. doi: 10.1016/s0378-3782(02)00111-1.

Reference Type BACKGROUND
PMID: 12614949 (View on PubMed)

Stephansson O, Dickman PW, Johansson A, Cnattingius S. Maternal weight, pregnancy weight gain, and the risk of antepartum stillbirth. Am J Obstet Gynecol. 2001 Feb;184(3):463-9. doi: 10.1067/mob.2001.109591.

Reference Type BACKGROUND
PMID: 11228504 (View on PubMed)

Wisborg K, Kesmodel U, Henriksen TB, Olsen SF, Secher NJ. Exposure to tobacco smoke in utero and the risk of stillbirth and death in the first year of life. Am J Epidemiol. 2001 Aug 15;154(4):322-7. doi: 10.1093/aje/154.4.322.

Reference Type BACKGROUND
PMID: 11495855 (View on PubMed)

Huang DY, Usher RH, Kramer MS, Yang H, Morin L, Fretts RC. Determinants of unexplained antepartum fetal deaths. Obstet Gynecol. 2000 Feb;95(2):215-21. doi: 10.1016/s0029-7844(99)00536-0.

Reference Type BACKGROUND
PMID: 10674582 (View on PubMed)

Cnattingius S, Haglund B, Kramer MS. Differences in late fetal death rates in association with determinants of small for gestational age fetuses: population based cohort study. BMJ. 1998 May 16;316(7143):1483-7. doi: 10.1136/bmj.316.7143.1483.

Reference Type BACKGROUND
PMID: 9582131 (View on PubMed)

Stacey T, Thompson JM, Mitchell EA, Ekeroma AJ, Zuccollo JM, McCowan LM. Association between maternal sleep practices and risk of late stillbirth: a case-control study. BMJ. 2011 Jun 14;342:d3403. doi: 10.1136/bmj.d3403.

Reference Type BACKGROUND
PMID: 21673002 (View on PubMed)

Budd J, Stacey T, Martin B, Roberts D, Heazell AEP. Women's experiences of being invited to participate in a case-control study of stillbirth - findings from the Midlands and North of England Stillbirth Study. BMC Pregnancy Childbirth. 2018 Aug 6;18(1):317. doi: 10.1186/s12884-018-1956-1.

Reference Type DERIVED
PMID: 30081858 (View on PubMed)

Heazell AEP, Budd J, Li M, Cronin R, Bradford B, McCowan LME, Mitchell EA, Stacey T, Martin B, Roberts D, Thompson JMD. Alterations in maternally perceived fetal movement and their association with late stillbirth: findings from the Midland and North of England stillbirth case-control study. BMJ Open. 2018 Jul 6;8(7):e020031. doi: 10.1136/bmjopen-2017-020031.

Reference Type DERIVED
PMID: 29982198 (View on PubMed)

Platts J, Mitchell EA, Stacey T, Martin BL, Roberts D, McCowan L, Heazell AE. The Midland and North of England Stillbirth Study (MiNESS). BMC Pregnancy Childbirth. 2014 May 21;14:171. doi: 10.1186/1471-2393-14-171.

Reference Type DERIVED
PMID: 24885461 (View on PubMed)

Other Identifiers

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GN2156

Identifier Type: -

Identifier Source: org_study_id

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