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Participants were required to be between 18 and 80 years old and be able to speak English, provide inform consent, and have DSM-IV-TR diagnostic confirmation of type I or II bipolar disorder or schizoaffective bipolar disorder (American Psychiatric Association 2000).
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Participating patients must provide informed consent.
Participants will provide informed written consent.
Participants have to provide informed written consent before randomisation.
All study communities, compounds and caregivers provide informed consent.
All participants provided informed consent.
All patients involved provided informed consent.
All patients provided informed written consent.
All the patients involved provided informed consent.
All participants provided informed written consent.
Each participant provided informed consent prior to study participation.
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