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Fig. 6 | BMC Health Services Research

Fig. 6

From: Communication and patient safety in gynecology and obstetrics - study protocol of an intervention study

Fig. 6

Trial design for Phase 3. Step 1: Participants (mothers-to-be/patients and their social support providers) are initially identified and screened for eligibility. All staff members are eligible for phase 3. Step 2: If eligible, participants give informed consent. Step 3: Pre-tests4. Step 4: Participants are provided with the Effective Communication App. Step 5: Post-tests5. Step 6: 3-months follow-up; person-specific pAEs are assessed after the patient gave birth. Possible reasons for participant drop-out have already been presented in Fig. 4/5. Note: 1 The comparator groups do not complete any tests again. Data acquisition in this group will be finished during Phase 2. 2 For inclusion/exclusion criteria, see Table 6. 3 Baseline data includes baseline assessments of pAE prevalence and costs. 4 Pre-test assessment includes demographic data, perceived social support, competences, training-related outcomes, subjective safety culture and treatment satisfaction. 5 Post-test assessments include perceived social support, competences and training-related outcomes. 6 At three months post-intervention, perceived social support, competences, behavior change as training-related outcome, subjective safety culture and treatment satisfaction will be assessed.

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