Methods | Randomised controlled trial. | |
Participants | 308 women with high-risk pregnancies (540 tests). | |
Interventions | 270 non-stress tests and 270 manual stimulation tests. | |
Outcomes | Incidence of non-reactive tests and time needed to produce a reactive test | |
Notes | Report in only Abstract form. | |
Risk of bias | ||
Bias | Authors’ judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not described. |
Allocation concealment (selection bias) | Unclear risk | Not described. |
Blinding of participants and personnel (performance bias) All outcomes |
High risk | Not blinded. |
Blinding of outcome assessment (detection bias) All outcomes |
Low risk | All fetal heart tracings were blindly reported by the same perinatologist who did not have information about the patients |
Incomplete outcome data (attrition bias) All outcomes |
Unclear risk | Unclear - data limited as report of trial in form of an Abstract |
Selective reporting (reporting bias) | Unclear risk | Unclear - data limited as report of trial in form of an Abstract |
Other bias | Unclear risk | Unclear - data limited as report of trial in form of an Abstract |