| Cohort Name |
The Million Women Study |
| Cohort Acronym |
Million Women |
| DOI |
Beral, V. (2017). Million Women [Data set]. Dementias Platform UK. https://doi.org/10.48532/032000 |
| Study Overview |
The Million Women Study is a national study of women’s health, involving more than one million UK women aged 50 and over. It is a collaborative project between Cancer Research UK and the National Health Service, with additional funding from the Medical Research Council and the Health and Safety Executive, which aims to answer many outstanding questions about the factors affecting women’s health in this age group. The main focus of the study relates to the effects of hormone replacement therapy use, but the large size of the study means that a very broad range of health issues can be addressed.
The Million Women Study is investigating how various reproductive and lifestyle factors affect women’s health. In particular, the study is looking at how hormone replacement therapy affects a woman’s breasts and other aspects of her health. Other factors being investigated include diet, exercise, employment patterns, oral contraceptive use, childbirth and breastfeeding, and family history of illness, in relation to a wide range of cancers and to other conditions such as fractures, gallbladder problems and cardiovascular disease. |
| #Subjects at Baseline |
1,300,000 (and 55,000 in the disease susceptibility study, started in 2006) |
| Institution Name |
The University of Oxford |
| Department Name |
Cancer Epidemiology Unit |
| City |
Oxford |
| Study/Database Website |
http://www.millionwomenstudy.org/ |
| Principal Investigator (PI) |
Prof Dame Valerie Beral |
| Key Study References |
Please see literature section |
| Population Based Study? |
Yes |
| Family Based Study? |
No |
| Clinical based sample? |
No |
| Is there follow-up data available? |
Yes |
| Were participants included prior to development of dementia (may refer to controls only)? |
Yes |
| Were participants included prior to development of MCI (may refer to controls only)? |
Yes |
| How is data collected? |
Combination of in person and postal |
| Who carries out data collection? |
Participants report on postal questionnaires and follow ups are done via data linkage. |
| Does this take place in participants' homes or at a central location? |
Home |
| Do participants take part individually or are families/partners involved? |
Individually |
| Dementia cases ascertained as part of study: |
No |
| Diagnosis based on review of existing clinical data |
No |
| Was diagnosis/primary outcomes made blind to exposure variables? |
No |
| How many times followed up? |
5 |
| Study start date |
01/01/1996 00:00:00 |
| Is study ongoing? |
Yes |
| Is study still recruiting? |
No |
| Inclusion criteria |
All screening centres in the NHS Breast Screening Programme (women in the age range 50-64 at recruitment) were eligible to collaborate in this research and all women invited for screening were eligible to take part. |
| Exclusion criteria |
Women who did not attend their breast screening appointment. |