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Treatment participants wishing to drop out of the study and wait-list participants demonstrating a need for immediate intervention will be withdrawn from the study and provided appropriate referral information.
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The immediate effects of the intervention will be assessed using the 12-week data.
The allocated intervention will be discontinued if there is evidence of an immediate serious adverse reaction such as anaphylaxis.
Immediate change and quarterly trend in clinical practices following the implementation of intervention will be also estimated.
Again, intervention will be too late.
The first intervention will be a personalized message intervention, the second intervention will consist of a biofeedback-based intervention.
Patients with acute severe mental symptoms that require immediate crisis interventions will be excluded.
Practical interventions will be necessary.
Interventions will be recorded.
It is also hypothesized that patients who are randomized to the 12-week lifestyle intervention at treatment start (immediate intervention) will experience improved symptom management following treatment compared to delayed intervention patients who begin the 12-week intervention following treatment.
Assignment to the immediate intervention and delayed intervention groups will be conducted at the site level rather than at the practitioner level or patient level.
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