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Although we are not seeking written consent from intervention participants, patients' responses to the consent question will be recorded on a datasheet, and those refusing consent will be excluded from the study and will have no further contact from the researchers.
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First they recorded on a tape recorder.
Recorded on a cassette.
Data were recorded on a standardized questionnaire.
Baseline characteristics, cause of referral, colonoscopic and capsule-endoscopic findings, technical data and results of the patient questionnaire were documented on a datasheet using Excel (Microsoft, Redmont, Washinton, USA).
(Someone recorded it on a video camera).
Record it on a cassette or CD.
Record on a wall calendar.
This data was recorded in the standard datasheets provided, alongside the date, duration, as well as initial and final coordinates of each tow.
GPs all performed non-pneumatic otoscopy ('Step 1') and documented their initial diagnosis, therapy and follow-up plan on a one-page datasheet based on this assessment alone.
Participants were also required to complete the experimental questionnaire, the external validity questionnaires (Medical Outcome Survey Short - SF-36, SGRQ-C, Hospitalization Anxiety Depression Scale - HADS, Physical Self-Worth - PSW) and a datasheet on their socio-cultural situation.
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