Icons / Login Created with Sketch.
Icons / User Created with Sketch.

Recruitment methods

All participants consented to joining the study and are free to withdraw or suspend their participation at any time with no need to provide a reason.

Original three birth cohorts (1921-26, 1946-51, 1973-78)

In April 1996, women in three age groups: 18-23 years (born 1973-78); 45-50 years (born 1946-51); and 70-75 years (born 1921-26) were selected from the Medicare database, which contains the name and address details of all Australian citizens and permanent residents. These women were sent an invitation to participate in the Australian Longitudinal Study on Women’s Health (ALSWH), and more than 40,000 responded and agreed to participate in the project for 20 years.

The three age groups were selected in order to follow women through life stages which are critical to women’s health and well-being. ALSWH began collecting information from the 1973-78 cohort when they were young women in the early stages of transition from late adolescence to full adulthood. Over time most of this group have moved into the workforce, entered adult relationships, and many have become mothers. The mid-age women, born 1946-51, were selected to examine menopausal transitions and the social and personal changes of middle age. The older women (born 1921-26) were selected when they were aged in their early seventies, an age when many were generally still active, involved members of the community. These women have been followed to obtain information on predictors of continuing well-being and independence in older adult life.

Sampling from the population was random within each age group, except that women from rural and remote areas were sampled at twice the rate of women in urban areas. This was done so that the numbers of women living outside major urban areas were large enough to allow statistical comparisons of the circumstances and health of city and country women, an important issue for Australia now and in the future. The Australian Longitudinal Study on Women’s Health is the largest study of health issues in rural and remote parts of Australia.

The longitudinal study design, by which the same women are followed for over 20 years, means that the study is able to observe changes in women’s health, to clarify cause-and-effect relationships and to assess the effects of changes in policy and practice. From 1996 to 2011, each age cohort was surveyed once every three years via surveys sent in the mail.

In 2011, the older cohort began receiving a shortened survey every six months, and in 2012 ALSWH began annual surveys of a new cohort of young women, born 1989-95.

For more information please refer to Technical Report 5, published December 1996 OR published paper:

Brown WJ, Bryson L, Byles JE, Dobson AJ, Manderson L, Schofield M & Williams G. Women’s Health Australia: Establishment of the Australian Longitudinal Study On Women’s Health. Journal of Women’s Health, 1996; 5(5): 467-472

1989-95 cohort

This cohort were recruited online, directly from the general population using multimedia strategies, as a pilot study revealed that the methodology used for the original three cohorts would not be successful.

For more information please refer to Section 4 of Technical Report 35, December 2012.

In the initial online survey participants indicated their consent to participate in the ALSWH study by completing the survey, consenting to data linkage and providing their personal details, which were validated by the Australian Department of Human Services.

Participants have been informed at each survey that researchers will be comparing their information with that collected in earlier surveys. Completion of the survey was taken as consent. This method of consent was approved by the Australian Department of Health, the Australian Department of Human Services, and both the University of Queensland (UQ) and the University of Newcastle (UoN) Human Research Ethics Committees (HRECs). At each wave, participants are offered the chance to win multiple prizes on completion of their survey. This was deemed necessary after consultations with women in the target age group in the planning phase of the study. Each prize draw has been approved by both UoN and UQ HRECs as appropriate compensation for participation. Participants have been and will be consistently informed that participation is voluntary and they are free to discontinue involvement at any time.

Surveys

All participants consented to joining the study and are free to withdraw or suspend their participation at any time with no need to provide a reason.

Health record linkage

  • Original three cohorts (1921-26, 1946-51, 1973-78). Participants who decline health record linkage are excluded from linked data requests. Over 80 percent of all participants have explicitly consented to record linkage. From 2005, the responsible HRECs have approved opt-out consent; in addition, a waiver applies to unconsented participants who were deceased or lost to follow up before 2005.
  • 1989-95 cohort. All participants expressly consented to health record linkage on recruitment in 2012/13. Those who subsequently opt out of record linkage are excluded from linked data requests.

PDF icon Please see Ethical considerations for publications for more information about participant consent.