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The majority of subjects in both arms completed a further array of questionnaires at 12 months after recruitment.
Similar(59)
Participants in both arms completed on-line international modules from the Collaborative Institutional Training Initiative.
Subjects randomized to the RE arm completed a 10 RM test.
GPs in the control arm completed a modified version of the questionnaire at 10 weeks post enrolment.
Patients in the docetaxel arm completed a median of 7.43 cycles and received a median cumulative total dose of 827.5 mg of docetaxel infusion; 12 (23.5 %) patients experienced a dose reduction and no patients experienced an interruption.
Patients in both study arms complete a battery of self-report questionnaires at equivalent moments in time for the first three assessments (T0: baseline; T1: 10 weeks after start of therapy (intervention group) or 13 weeks after randomization (control group); and T2: post-treatment (intervention group) or 23 weeks after randomization (control group), see Figure 1).
Participants in both arms complete assessments at baseline, one year and two years after inclusion.
In both arms complete disappearance of acute mucositis was noted by 8 10 weeks.
Participants in both arms complete assessments at baseline (Time 1), 6-month follow-up (Time 2), and 12-month follow-up (Time 3).
Almost all patients (>97%) in both treatment arms completed the 5 weeks of radiotherapy.
Both intervention arms completed assessments at baseline, 3, and 9 months.
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