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Regardless of any decision to modify or discontinue their assigned intervention, study participants should be retained in the trial whenever possible to enable follow-up data collection and prevent missing data (Item 18b).
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This model controlled for age (in 5-year increments), gender, physical activity (MET-h/w) quartiles, body mass index quartiles, history of smoking (never, past, current), history of hypertension, history of high cholesterol, parental history of diabetes, alcohol use (mg/week) quartiles, and assigned intervention (health promotion) of the original study.
A limitation of this study is the validity of the incretin hormone responses that were obtained after the assigned interventions.
Patient expectation was evaluated as confidence in the success of assigned study intervention using Interstudy's Low Back Pain TyPE Specification instrument [ 29].
For a given patient, the assigned study intervention will be discontinued at the discretion of the trial investigators if the healthcare staff members notice a change in behaviour occurring in the patient or the symptom burden is too high.
In case of established delirium or if the assigned study intervention is thought to have a direct influence on the patient's treatment, the treating physician will request for unblinding and may further decide on treatment.
151 For a given trial participant, the assigned study intervention may need to be modified or discontinued by trial investigators for various reasons, including harms, improved health status, lack of efficacy, and withdrawal of participant consent.
We present means and frequencies to describe the baseline characteristics of both patients and relatives assigned to the control and intervention study groups.
Also within NVivo, each case (intervention study) was assigned codes for the following attributes: (1) whether or not the intervention results were published, (2) whether or not there were statistically significant intervention effects on primary outcomes, and (3) whether or not there were post-study impacts.
All primary care physicians in Manitoba, Canada have been randomly assigned to a control group or an intervention study group.
There were 18 women in both the intervention and non-intervention arms of the intervention study who had been randomly assigned.
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