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Trial registered on ANZCTR
Registration number
ACTRN12621000179831
Ethics application status
Approved
Date submitted
8/12/2020
Date registered
22/02/2021
Date last updated
22/02/2021
Date data sharing statement initially provided
22/02/2021
Type of registration
Retrospectively registered
Titles & IDs
Public title
The impact of Australian bushfires on pregnant and breastfeeding women in the Mid North Coast Local Health District (MNCLHD) New South Wales.
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Scientific title
The health impact of Australian bushfires on pregnant and breastfeeding women with and without asthma, in the MNCLHD.
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Secondary ID [1]
302959
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None
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Universal Trial Number (UTN)
U1111-1262-4642
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Trial acronym
Nil known
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Linked study record
Nil known
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Health condition
Health condition(s) or problem(s) studied:
Respiratory symptoms
320023
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Maternal wellbeing
320025
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Pregnancy
320364
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Breast feeding
320815
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Asthma
320816
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Condition category
Condition code
Public Health
317944
317944
0
0
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Other public health
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Respiratory
318639
318639
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0
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Asthma
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Reproductive Health and Childbirth
318640
318640
0
0
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Other reproductive health and childbirth disorders
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Reproductive Health and Childbirth
318643
318643
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0
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Breast feeding
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
This study is a cross-sectional survey with longitudinal follow up of pregnant and/or breastfeeding women with asthma and without asthma, and health outcomes of their infants. The aim is to better understand the experiences and impacts of the 2019/2020 bushfires on the health and wellbeing of this population. Further, it also examines the impacts on this cohort leading into the 2020/2021 bushfire season, notably evaluating wellbeing, and maternal concerns and behaviours (e.g. exposure reduction strategies, medication use, and infant feeding practices).
The study will be conducted primarily online using REDCap survey software. The survey will be distributed to participants who have registered and provided informed consent using a web-based platform, paper-based survey or verbally (via telephone). Participants will receive a web-link via email or telephone call to complete the survey.
Follow up surveys will also be conducted in January and May 2021, exploring the impact on this cohort regarding their preparedness, health and wellbeing during the subsequent 2020/2021 bushfire season. Participants will receive a follow-up survey invitation (via email or text message), providing information on accessing the follow-up survey through an online link, mailed out a paper-based survey or via a telephone call. The initial questionnaire will take approximately 25-30 minutes to complete. Follow-up surveys will take approximately 20 minutes each. The initial survey was administered on 28th December 2020.
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Intervention code [1]
319259
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Not applicable
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Comparator / control treatment
no control group.
Women without asthma are a reference group.
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Control group
Active
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Outcomes
Primary outcome [1]
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Composite primary outcome:
The experiences of women with and without asthma who were pregnant and/or breastfeeding during the 2019/20 bushfire season, notably evaluating the impact of smoke exposure on respiratory symptoms, wellbeing, and maternal concerns and behaviours (e.g. exposure reduction strategies, medication use, and infant feeding practices) through baseline and follow up surveys.
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Assessment method [1]
325952
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Timepoint [1]
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At the completion of all surveys.
Participants completed the baseline survey on 7 January 2021.
Follow-up survey 1 from 18 January to 31 March 2021.
Follow-up survey2 from 17 May to 31 July 2021.
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Secondary outcome [1]
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Assess the impact of bushfire smoke exposure on infant health through baseline and follow up surveys.
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Assessment method [1]
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Timepoint [1]
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At the completion of all surveys. Participants completed the baseline survey on 7 January 2021.
Follow-up survey 1 from 18 January to 31 March 2021.
Follow-up survey2 from 17 May to 31 July 2021.
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Eligibility
Key inclusion criteria
All women that meet the inclusion criteria below;
1. Women 18 years of age or older
2. Residing in MNCLHD, NSW, Australia during the 2019/2020 Bushfire season, between July 2019 – March 2020.
3. Pregnant and /or breastfeeding during the 2019/2020 Bushfire season
4. For the asthma group, a previous doctor diagnosis of asthma is required
5. If you are completing this as a non-asthma participant this means you do not or never have had a diagnosis of asthma
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
None
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Descriptive statistics will be used to describe the demographic characteristics, general health and pregnancy and breastfeeding practice of the study participants. Exposure estimates (particulate matter) will be reported as medians with interquartile ranges (IQR). The exposure data will be assigned according to the participant's residence. Outcome data collected during the bushfire season and subsequent bushfire period will be compared between study participants. Differences between study participants will be ascertained utilizing Pearson’s chi-squared (for categorical variables) and independent t-test (for continuous variables).
The multivariable log-binomial generalized linear regression model will be used to estimate the impact of bushfire smoke exposure on self-reported health outcomes during the 2019/2020 Australian bushfire season compared to post bushfire season. The model fit will be assessed by applying Hosmer – Lemeshow, the person chi-square and the unweighted sum of squares test. Further, Akaike information criteria (AIC) will be applied to inform model selection. Overall effects will be assessed using the risk ratio (RR) and 95% confidence intervals (95% CI) for self-reported health outcomes. Further, stratified analysis by history of asthma will be performed to assess the different effects of bushfire smoke exposure on women with asthma and without asthma.
The effect of bushfire smoke exposure on self-reported health outcomes during 2019/20 bushfire season compared to 2020/2021 bushfire season will be examined using generalized linear regression model. RR with 95% CI will be used to determine the strength of the association. Sensitivity analysis will be conducted to examine the soundness of the findings, which includes restricting the analysis to women with asthma and who seek health advice during the bushfire season. Further, separate analysis will be performed to evaluate the possible difference in women who take actions to reduce exposure to smoke during the bushfire seasons.
The State-Trait Anxiety Inventory for Adults (STAIAD) will be used to assess women wellbeing (anxiety level) during and after the 2019/2020 bushfire season. The current study will employ STAIAD consists of six items with a response based on a self-reported four-point Likert scale (“Not at all”, “Somewhat”, “Moderately so”, “Very much so”). Standardized cut-off scores will be used to assess the level of anxiety. A higher score of STAIAD indicates a higher level of anxiety. The multivariable linear regression model will be used to calculate the RR for the level of anxiety associated with bushfire smoke during the 2019/2020 bushfire season compared to post bushfire. Further, the impact of bushfire smoke on anxiety level during 2019/20 bushfire season compared to 2020/2021 bushfire season will be reported using RR with 95% CI. A separate analysis will also be performed to determine the association between bushfire smoke exposure and level of anxiety for women with asthma and without asthma.
The association between women exposure to bushfire smoke and pregnancy outcomes, such as gestational diabetes, pregnancy-induced hypertension, low birth weight, preterm birth and parent-reported infant health outcomes will be calculated using generalized linear regression model. The results will be reported as RR with 95% CIs. Stratified analysis by a history of asthma will also be employed to assess the effects of exposure to bushfire smoke on parent-reported health outcomes.
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
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Actual
27/11/2020
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Date of last participant enrolment
Anticipated
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Actual
7/01/2021
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Date of last data collection
Anticipated
31/07/2021
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Actual
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Sample size
Target
261
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Accrual to date
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Final
51
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Recruitment in Australia
Recruitment state(s)
NSW
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
307377
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University of Newcastle
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Address [1]
307377
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Faculty of Health and Medicine
University of Newcastle
Hunter Medical Research Institute, 1 Kookaburra Circuit, New Lambton Heights, NSW, 2305
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Country [1]
307377
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Australia
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Primary sponsor type
Individual
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Name
Professor Vanessa M. McDonald
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Address
School of Nursing and Midwifery
Faculty of Health and Medicine
University of Newcastle
Level 2 Hunter Medical Research Institute, 1 Kookaburra Circuit, New Lambton Heights, NSW, 2305
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Country
Australia
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Secondary sponsor category [1]
308048
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None
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Name [1]
308048
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Address [1]
308048
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Country [1]
308048
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
307464
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North Coast NSW Human Research Ethics Committee
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Ethics committee address [1]
307464
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PO Box 821 Murwillumbah NSW 2484
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Ethics committee country [1]
307464
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Australia
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Date submitted for ethics approval [1]
307464
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Approval date [1]
307464
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28/10/2020
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Ethics approval number [1]
307464
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HREA297
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Summary
Brief summary
The 2019/2020 bushfire season has had a widespread impact on the health and wellbeing of people in Australia. Exposure to air pollutions, such as bushfire smoke, during pregnancy and early childhood is associated with health impacts later in childhood. Additionally, pregnant and breastfeeding women with respiratory conditions, such as asthma, are particularly vulnerable to bushfire smoke exposure. The purpose of the research is to investigate the impacts of bushfire smoke exposure on health outcomes of vulnerable groups (pregnant and breastfeeding women) with and without asthma, particularly evaluating the impact of smoke on respiratory symptoms, wellbeing, and maternal concerns and behaviours ( e.g. exposure reduction strategies, medication use, and infant feeding practices). The information from this project will inform guidelines and health messages (developed and disseminated with our partner groups) for pregnant and breastfeeding women with and without asthma, and healthcare providers. Further, it enhances bushfire preparedness and responses by explaining effective preventive strategies to reduce smoke exposure and treatment. Women who agree to participate in this study will fill out a baseline survey online, via telephone or a paper-based copy. After completing the baseline survey, participants will be invited to complete two follow up surveys during and after the next bushfire season in 2020/202. The follow-up surveys will also be via online, via telephone or paper-based options.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Prof Vanessa M. McDonald
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Address
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Professor of Nursing
School of Nursing and Midwifery
Faculty of Health and Medicine
University of Newcastle
Level 2 Hunter Medical Research Institute, 1 Kookaburra Circuit, New Lambton Heights, NSW 2305.
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Country
107326
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Australia
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Phone
107326
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+61 02 4042 0146
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Fax
107326
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Email
107326
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[email protected]
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Contact person for public queries
Name
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Tesfalidet Beyene
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Address
107327
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Postdoctoral Research Fellow
School of Medicine and Public Health
University of Newcastle
University Drive, Callaghan, NSW,2308
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Country
107327
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Australia
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Phone
107327
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+61 02 4042 0764
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Fax
107327
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Email
107327
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[email protected]
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Contact person for scientific queries
Name
107328
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Tesfalidet Beyene
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Address
107328
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Postdoctoral Research Fellow
School of Medicine and Public Health
University of Newcastle
University Drive, Callaghan, NSW,2308
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Country
107328
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Australia
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Phone
107328
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+61 02 4042 0764
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Fax
107328
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Email
107328
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
No individualised data will be available on completion of the study.
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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