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Baseline information such as demographic data, medical history, life style and medication history were collected.
On study enrolment, baseline information such as history of asthma or any other allergic diseases is collected via the web-based questionnaire.
Data collection was three-fold: (i) collection of baseline information such as TB policies, (ii) conduction of semi-structured in-depth interviews; and (iii) observations made at the health care organizations.
Even in disasters which start slowly and are prolonged, baseline information such as population-at-risk cannot be collected within a short timeframe, and hence must be available on an on-going basis prior to the disaster.
As described earlier [ 17], we found that the pairs were well matched for baseline information, such as gender (34 males and 11 females), age, and smoking habits (26 ex- or present smokers and 19 nonsmokers), with a mean age of 40.6 in both the BD-exposed group and the control group.
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The assessment collected self-reported demographic information (including race/ethnicity), baseline clinical information (such as length of time HIV-positive), and screened participants for drug, alcohol, and sexual risks.
Such studies may not fulfill all standard criteria set for inclusion in the meta-analysis and yet they have baseline morbidity information such as parasitological data that could be useful in predicting future outcomes.
Between March and October of 2008, we collected baseline sociodemographic information, such as parental education and occupations, home construction characteristics, and availability of television, through a structured parent interview.
The initial data collected at baseline included demographic information, such as age, gender, marital status, race, ethnicity, and number of people within the home, as well as functional status, QOL, and comorbid health conditions as defined by the ERA score at study entry.
The baseline assessment captured sociodemographic information such as race/ethnicity, marital status, educational status, and insurance status.
The third phase (denominator population) was to construct an anonymised clinical data archive for the study five year period for the total baseline cohorts, linking clinical information such as diagnosis, prescriptions and referrals.
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