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Losses in long-term studies may be due to refusals to continue in a study, inability to trace individuals for follow-up, and deaths.
In our study, inability to pay comes out as one of the major reasons for failure to enroll into the scheme.
Exclusion criteria include those unable to give informed consent to participate in the study, inability to understand and communicate in English, and members of the public from vulnerable groups (those under 18, prisoners, those in dependent relationships, the mentally ill).
Reduced compliance with the Conner's Parents Rating Scale may have resulted from resource limitations of the present study (inability to send out second mailings to parents), or may indicate that this scale has low practical utility and may be unsuitable for future studies.
Exclusion criteria included lack of consent to participate in the study, inability to understand or complete the questionnaires, severe arthritic changes, recent (up to 2 years) fractures and diseases having significant morbidity and a severe impact on HRQoL including cancer, congestive heart failure, and significant lung, renal, or liver diseases.
a history of severe adverse reaction or known hypersensitivity to maltose and/or silicon dioxide; patients requiring hospitalization; use of any investigational drug and/or participation in any clinical trial within 3 months before entering this study; inability to give a valid written informed consent or to properly follow the protocol.
Similar(53)
Many victims reported academic difficulties including absenteeism, interrupted studies, inability to concentrate or study and loss of self-confidence.
Exclusion criteria: intracranial disorder, other than migraine, head trauma in the previous year, pregnancy or lactation during study period, inability (according to the investigators judgment) to fill a headache diary.
Limitations to the study include inability to infer causal relationships because of the cross-sectional nature of the data.
The exclusion criteria for cases were: refusal to participate in the study and inability to provide informed consent.
Assessing the possible benefit of the etanercept gene is further hindered by the study's inability to measure etanercept protein accurately in humans.
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