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The completion of the WHOQOL-Bref, the BDI and attitudes of caregivers' questionnaires by the subjects was supervised by a trained female Arab research assistant.
In order to minimize the burden of data collection on patients and family caregivers, questionnaires and diaries have a short completion time and the total duration of interviews will be limited to a maximum of 60 minutes.
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The PA questions included in the primary caregivers questionnaire were adapted from the Leisure Time Exercise Questionnaire [ 25].
The caregivers' questionnaire will also include questions on the variability of the type and 'level' of care provided (e.g., types of tasks and the time involved).
All remaining data on sociodemographic and other clinical details, health and social care utilization and caregiving hours, were collected via structured caregiver questionnaires.
In prospective COI studies, events have not occurred yet, so data collection is done by the patients' follow-up, medical records, data from clinical trials and patients or caregiver questionnaires.
Data on productivity losses will be obtained using the structured caregiver questionnaires.
Caregiver questionnaires (three copies) were sent to the patients, asking them to pass the questionnaires on to one to three adult caregivers involved in their disease course.
This means employing more than one class of measure - not just a biomarker, but judgment-free tests (such as neuropsychological ones) and judgment-based tests (such as clinical interviews, and patient and caregiver questionnaires).
The Impact of Alzheimer's Disease on Caregiver Questionnaire (IADCQ) is an instrument used to measure the burden of caregiving and includes items that represent the key concepts and domains of caregiving for an AD patient.
To evaluate the psychometric properties of the Care and Comfort Caregiver Questionnaire (CareQ), which was developed to measure the perceived effort of caregivers in providing care for children with moderate to severe cerebral palsy (CP).
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