1.
CONSORT 2010 checklist of information to include when reporting a randomised trial*.
2.
Research protocol.
Dataset.
The CONSORT flow diagram.
The equipment used for both the HALF-MIS treatment and the higher frequency variant in a clinical setting.
Descriptive characteristics per group at baseline (Mean ± SD or Median [IQR], except for sex).
Pain intensity and analgesic use per group and for total sample before the first treatment (T0), after the last treatment (T1) and at follow-up (T2) (Mean ± SD or Median [IQR]).
Secondary outcomes per group and for total sample before the first treatment (T0), after the last treatment (T1) and at follow-up (T2) (Median [IQR]).
Parameter estimates of the fixed effects of the final model predicting pain intensity.
Characteristics of victims and nonvictims.