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The heterogeneity and inconsistency between trials will be assessed by the I statistical test and Cochrane's Q test.
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The trials will be held next month.
The initial trials will be in San Francisco and New York.
Three trials will be performed.
Quasi-randomised trials will be excluded.
Trials will be nested within-subject.
Only successful trials will be kept.
Ideally, randomised controlled trials will be conducted.
Five successful walking trials will be recorded.
To ensure that subgroup effects are not confounded by between-trial differences, dependency between data originating from the same trial will be taken into account using a random intercept for every study in the regression model [ 18].
Women participating in the PREPARE trial will be between the ages of 18 and 41 years, with a body mass index (BMI) between 20 and 32 kg/m, and undergoing their first or second cycle of IVF or in vitro fertilisation – intracytoplasmic sperm injection (IVF-ICSI).
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