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Participants were allocated into 17 dyads.
Participants were allocated in three groups.
Participants were allocated to 5 groups (G1 G5).
Participants were allocated to 2 groups according to the direction of the shunt.
The research assistant ensured that appropriate interventions were carried out depending on the group to which the participants were allocated.
The trial was double-blinded, so neither trial staff nor participants knew to which gel group participants were allocated.
Participants were allocated to CBGT or ICBT in a 1∶1 ratio using simple randomization with no restrictions or matching.
Eligible participants were allocated to receive one of the study combinations in early September, early October and early November 2004.
Seventeen participants were allocated to each group.
All participants were allocated a trial number.
37 Fifty-three participants were allocated to the study.
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