Significance of Data collection
Data collection is a systematic process essential for various research studies, involving gathering information from different sources. It includes techniques such as primary data collection, patient interviews, surveys, and observations to evaluate treatments or analyze health outcomes. In Ayurveda, for example, data collection includes obtaining informed consent while assessing patients' health without disrupting clinical practices. The process also encompasses the review of historical texts and methodologies, reinforcing the importance of accurate data in drawing meaningful conclusions in both clinical and research settings.
Synonyms: Data gathering, Data collection process, Data acquisition, Information collection, Data aggregation
In Dutch: Gegevensverzameling; In Finnish: Tiedonkeruu; In Spanish: Recopilación de datos; In German: Datenerfassung
The below excerpts are indicatory and do represent direct quotations or translations. It is your responsibility to fact check each reference.
Hindu concept of 'Data collection'
Data collection in Hinduism encompasses gathering comprehensive medical and research information through various methods, including observations and surveys, while focusing on qualitative data to analyze treatment effectiveness, integrating traditional Ayurvedic practices alongside modern research techniques.
(1) Data collection is performed on an observational basis in the front office and radiology departments, as specified in the methodology of the study according to the text.[1] (2) Data collection involved examining patients, as per the Case Record Form, and the information was written in the CRF and collected for analysis.[2] (3) This term refers to the process of reviewing classical Ayurvedic texts like Charaka Samhita, Sushruta Samhita, and Ashtanga Hridaya.[3] (4) This is the process of gathering information for a study, including measurements, observations, and patient reports, used to analyze the effectiveness of a treatment.[4] (5) The methods used to gather information included general examination and a research proforma, including a Nidana Panchaka Patraka, consent form, and a sphygmomanometer.[5]
(1) The process of gathering information and sources pertinent to medical history which aids in understanding the evolution of medical practices.[6]
The concept of Data collection in scientific sources
Data collection involves systematically gathering information from participants using various methods such as questionnaires and interviews. It is crucial in research for evaluating findings, ethical compliance, and assessing safety, particularly in pharmacovigilance and medical studies.
(1) This refers to the period of time during which the study was gathering information, with patients recruited from the Paediatric Clinic at Sarawak General Hospital.[7] (2) This is the process that occurred from November 2020 to January 2021, where adolescents were invited to answer an online questionnaire disseminated through various platforms.[8] (3) This process took place between November 2010 and March 2011, with the participants completing a personal information form and the Nutrition Quality of Life instrument.[9] (4) This is the process of gathering information for the study, which needs to be clearly described in the articles selected.[10] (5) This refers to the process of gathering information for the study, and specific individuals were involved in collecting and assembling the data.[11]
(1) A 33-item close-ended questionnaire was used for this process, and it took approximately 20 minutes to complete, with the questionnaire divided into six parts.[12] (2) The text explains the methods used for data collection, including the use of an electronic questionnaire and the inclusion of samples from hospitals and health centers in N’Djamena.[13] (3) The process of gathering information for the study, which involved the use of non-probability sampling and the distribution of survey forms to doctors who met the inclusion criteria.[14]
(1) This refers to the process of gathering information from hospital records, and the authors acknowledge the assistance of healthcare staff in this process.[15] (2) This outlines the process of gathering information for the study, which involved in-depth interviews guided by a semi-structured questionnaire.[16] (3) The exclusion criteria were ruled out through review of participants’ case notes and interviews, and information was obtained by the authors using an interviewer-administered questionnaire, which had two sections: socio-demographic variables and clinical factors.[17]
(1) The 57-question survey was administered on Survey Monkey (an online survey company); the survey was open from December 2016 to June 2017.[18]
(1) The process of gathering information from the residents, using a structured questionnaire administered through face-to-face interviews by the principal investigator.[19]
(1) This action involves gathering information for research, including the process of systematically obtaining relevant details and information to be analyzed, interpreted, and used to draw conclusions.[20] (2) Data were collected between 01 October 2019 and 31 December 2019, and sociodemographic and clinical data and BPRS-E scores were collected, according to the provided text.[21] (3) This is the process of gathering information using self-administered questionnaires such as the Beck's Depression Inventory, Hopelessness Scale, Suicide Ideation Scale, and Anxiety Inventory.[22] (4) Data collection involves gathering information from patient files, including demographic data, diagnoses, and psychosocial stressors reported during consultations.[23] (5) This refers to the process of gathering information for the study, and in this case, data was collected using questionnaires and surveys completed by mental healthcare practitioners during a specific time frame.[24]