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. 2018 Sep 28;2018(9):CD005528. doi: 10.1002/14651858.CD005528.pub3

Rouhe 2013.

Methods Randomised trial
Participants Finland
Inclusion criteria: nulliparous women with severe fear of birth according to the Wijma Delivery Expectancy Questionnaire A (prenatal version) (W‐DEQ A) (REF 21)
Interventions Intervention: psychoeducative group sessions led by a psychologist
Women in the control group received a letter in which they were advised to discuss their fear of childbirth in their primary maternity healthcare unit. When needed, primary health care referred fearful women to a special maternity care unit
Outcomes Mode of delivery, life satisfaction and general well‐being, costs, duration of labour and delivery, postpartum haemorrhage, usage of epidural or spinal analgesia, birthweight and umbilical arterial pH of the new born, Apgar scores, and interventions during the third stage of labour (suturing or surgical evacuation of placenta or membranes postpartum)
Notes Baseline (control group) CS rate: 32.5%
Date of study: October 2007 to August 2009
Funding: Emil Aaltonen Foundation and the Signe and Ane Gyllenberg Foundation
Conflict of interest: the authors declare that they have no known conflict of interests.
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Method of allocation sequence generation not reported (Women were randomised, by one of the researchers, to the intervention or control group in the proportion of 1:2 in balanced blocks of 18)
Allocation concealment (selection bias) Low risk Sealed opaque envelopes used
Blinding of participants and personnel (performance bias) 
 All outcomes Unclear risk No information provided in the report
Blinding of outcome assessment (detection bias) 
 All outcomes Low risk Main outcomes (mode of delivery) objective
Baseline characteristics similar? Low risk Table 3 in the article: There were no significant differences between study groups in age, social status, education, previous pregnancies or marital status
Baseline outcome measurements similar? Unclear risk No information provided
Incomplete outcome data (attrition bias) 
 All outcomes Low risk No missing data
Selective reporting (reporting bias) Low risk Data on all prespecified outcomes reported
Protected against contamination? Unclear risk Insufficient information available to assess likelihood of contamination
Other bias Low risk No evidence of other bias