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1.
BMC Med Res Methodol ; 19(1): 235, 2019 12 11.
Article in English | MEDLINE | ID: mdl-31829134

ABSTRACT

BACKGROUND: Consent to link survey data with health-related administrative datasets is increasingly being sought but little is known about the influence of recruiting via online technologies on participants' consents. The goal of this paper is to examine what factors (sociodemographic, recruitment, incentives, data linkage information, health) are associated with opt-in consent to link online survey data to administrative datasets (referred to as consent to data linkage). METHODS: The Australian Longitudinal Study on Women's Health is a prospective study of factors affecting the health and well-being of women. We report on factors associated with opt-in consent to data linkage at the end of an online survey of a new cohort of 18-23 year old Australian women recruited in 2012-13. Classification and Regression Tree analysis with decision trees was used to predict consent. RESULTS: In this study 69% consented to data linkage. The provision of residential address by the individual, or not (as a measure of attitudes towards privacy), was the most important factor in classifying the data into similar groups of consenters (76% consenters versus 47% respectively). Thereafter, for those who did not provide their residential address, the incentives and data linkage information that was offered was the next most important factor, with incentive 2: limited-edition designer leggings and additional information about confidentiality showing increases in consent rates over Incentive 1: AUD50 gift voucher: 60% versus 37%. CONCLUSIONS: In young Australian women, attitudes towards privacy was strongly associated with consenting to data linkage. Providing additional details about data confidentiality was successful in increasing consent and so was cohort appropriate incentives. Ensuring that prospective participants understand the consent and privacy protocols in place to protect their confidential information builds confidence in consenting to data linkage.


Subject(s)
Confidentiality , Information Storage and Retrieval , Informed Consent , Internet , Medical Record Linkage , Women's Health , Adolescent , Attitude , Australia , Female , Humans , Longitudinal Studies , Surveys and Questionnaires , Young Adult
2.
Phys Ther ; 101(3)2021 03 03.
Article in English | MEDLINE | ID: mdl-33336703

ABSTRACT

OBJECTIVE: Serratus anterior (SA) muscle activation may be decreased with subacromial pain syndrome. The purpose of this study was to determine whether the addition of real-time ultrasound (RTUS) visual feedback increased activation of SA in adults with painful shoulders in comparison to manual facilitation alone. METHODS: This assessor-blinded, 2-period, randomized cross-over trial was conducted in a university medical imaging laboratory. Adults with mild-moderate unilateral subacromial pain received both interventions in random order with at least 1-week washout between interventions. Fourteen participants were randomized to receive manual facilitation with RTUS first, and 13 were randomized to receive manual facilitation alone first. Fifteen repetitions of a supine ``serratus punch'' were facilitated by RTUS visual feedback with manual facilitation or by manual facilitation alone. Levels of SA activation via surface electromyography were normalized to a maximum voluntary isometric contraction. RESULTS: A total of 25 participants completed the full trial of both interventions. Data from 25 participant periods for RTUS with manual facilitation and data from 26 participant periods for manual facilitation only were analyzed. The predicted marginal mean difference between interventions was 55.5% (95% CI = 13.9% to 97.1%) in favor of the addition of RTUS feedback. No adverse effects occurred. CONCLUSION: RTUS visual feedback increases SA activation in adults with painful shoulders compared with manual facilitation alone. IMPACT: Determining if RTUS can improve SA muscle activation may help clinicians improve physical therapist interventions for subacromial pain syndrome.


Subject(s)
Feedback, Sensory/physiology , Muscle, Skeletal/diagnostic imaging , Shoulder Pain/diagnostic imaging , Shoulder Pain/rehabilitation , Ultrasonography , Adult , Aged , Cross-Over Studies , Electromyography , Female , Humans , Male , Middle Aged , Muscle, Skeletal/physiopathology , Shoulder Pain/physiopathology , Single-Blind Method
3.
J Sci Med Sport ; 21(2): 129-133, 2018 Feb.
Article in English | MEDLINE | ID: mdl-28778823

ABSTRACT

OBJECTIVES: To compare serratus anterior and lower trapezius muscle thickness between swimmers with and without current shoulder pain, and between sides when measured by real-time ultrasound imaging. DESIGN: A single blinded age and gender-matched case-control study with 26 symptomatic and 26 asymptomatic recreational swimmers. METHODS: Muscle thickness of serratus anterior and lower trapezius were measured using previously validated real-time ultrasound imaging protocols. Serratus anterior thickness was measured in side lying with 90° of glenohumeral flexion at rest and during a scapular protraction contraction. Lower trapezius thickness was measured in prone with 145° of glenohumeral abduction whilst at rest and when holding the weight of the arm. RESULTS: There was no statistically significant difference between the muscle thickness of serratus anterior and lower trapezius between the symptomatic shoulder and the dominance-matched shoulder in the asymptomatic group of swimmers. There was also no significant difference in muscle thickness between the symptomatic side and asymptomatic side within the symptomatic group. CONCLUSIONS: There appears to be no difference in serratus anterior and lower trapezius thickness between swimmers who have mild to moderate shoulder pain, who continue to swim and those who do not have shoulder pain. When imaging the serratus anterior and lower trapezius in swimmers with mild shoulder pain, clinicians should expect no differences between sides. If muscle thickness differences between sides are detected in recreational swimmers, this may indicate that the swimmer is participating in other asymmetrical activities or has a higher level of shoulder pain.


Subject(s)
Muscle, Skeletal/physiology , Shoulder Pain/etiology , Swimming/physiology , Adult , Case-Control Studies , Female , Humans , Isometric Contraction/physiology , Male , Middle Aged , Muscle, Skeletal/diagnostic imaging , Range of Motion, Articular/physiology , Shoulder/physiology , Single-Blind Method , Ultrasonography
4.
J Clin Epidemiol ; 68(8): 870-6, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25700941

ABSTRACT

OBJECTIVES: To examine bias arising from loss to follow-up due to lack of contact. STUDY DESIGN AND SETTING: The 1973-1978 cohort of Australian Longitudinal Study on Women's Health was first surveyed in 1996 and followed up in 2000, 2003, 2006, and 2009. At the 2000 survey, 9,688 women responded (responders), 2,972 could not be contacted, of whom 1,515 responded subsequently (temporary no contact) and 1,457 did not (permanent no contact). Characteristics were compared for these groups at baseline and follow-up in 2003, 2006, or 2009. Relative risk ratios were used to estimate bias. RESULTS: No-contacts were younger, more likely to live in cities, to be less educated and stressed about money than responders. No-contacts were more likely to be in de facto relationships, separated, divorced, or widowed, to have experienced partner violence and be smokers. Compared with temporary no contact, permanent no contact were less educated, less likely to be studying or employed. Despite differences in prevalence estimates, relative odds ratios were close to one and had confidence intervals that included one, indicating little effect of bias. CONCLUSION: Although various characteristics were related to loss to follow-up, the relative risks estimates did not indicate serious bias due to loss to follow-up in this cohort of young women.


Subject(s)
Epidemiologic Methods , Health Surveys , Lost to Follow-Up , Adolescent , Adult , Australia/epidemiology , Bias , Demography , Female , Health Behavior , Humans , Longitudinal Studies , Research Design , Risk Factors
5.
Aust N Z J Public Health ; 39(6): 518-23, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26094708

ABSTRACT

OBJECTIVE: To evaluate the impact of drought on the mental health of rural Australian women and those in vulnerable sub-populations: women who were more isolated, poorer and less educated; and women who had histories of chronic disease or poor mental health. METHODS: Surveys were mailed in 1996, 1998, 2001, 2004 and 2008 to 6,664 women born between 1946 and1951 who were participating in the Australian Longitudinal Study on Women's Health. The surveys included the Mental Health Index of the Medical Outcomes Study Short-Form 36 (MHI). Drought was assessed by linking the latitude and longitude of women's place of residence at each survey to the Hutchinson Drought Index. Associations between MHI and drought were assessed using linear mixed-models. RESULTS: While 31% of the women experienced drought in 1998 and 50% experienced drought in 2007; experience of droughts was less common in the other years. Although drought varied from survey year to survey year, mental health did not vary with drought conditions for rural women or vulnerable sub-populations. CONCLUSIONS: These findings are contrary to the long-held assumption that droughts increase mental health problems in Australia. IMPLICATIONS: While similar results may not be true for men, empirical evidence (rather than assumptions) is required on associations between drought and mental health.


Subject(s)
Droughts , Mental Health , Rural Population , Vulnerable Populations , Women's Health , Australia , Female , Health Surveys , Humans , Longitudinal Studies , Middle Aged , Socioeconomic Factors , Stress, Psychological
6.
Health Aff (Millwood) ; 30(8): 1451-60, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21821562

ABSTRACT

Hispanics are more likely than any other racial or ethnic group in the United States to lack health insurance. This paper draws on quantitative and qualitative research to evaluate the extent to which health reforms in Massachusetts, a model for the Affordable Care Act of 2010, have reduced disparities in insurance coverage and access to health care. We found that rates of coverage and the likelihood of having a usual provider increased dramatically for Massachusetts Hispanics after the state's reforms, but disparities remained. The increase in insurance coverage among Hispanics was more than double that experienced by non-Hispanic whites. Even so, in 2009, 78.9 percent of Hispanics had coverage, versus 96 percent of non-Hispanic whites. Language and other cultural factors remained significant barriers: Only 66.6 percent of Hispanics with limited proficiency in English were insured. One-third of Spanish-speaking Hispanics still did not have a personal provider in 2009, and 26.8 percent reported not seeing a doctor because of cost, up from 18.9 percent in 2005. We suggest ways to reduce such disparities through national health care reform, including simplified enrollment and reenrollment processes and assistance in finding a provider and navigating an unfamiliar care system.


Subject(s)
Health Care Reform , Health Services Accessibility , Healthcare Disparities , Hispanic or Latino , Adolescent , Adult , Female , Focus Groups , Health Care Surveys , Humans , Insurance Coverage , Insurance, Health , Interviews as Topic , Male , Massachusetts , Middle Aged , Patient Protection and Affordable Care Act , Young Adult
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