Psychological Distress Clinical Trial
Official title:
Testing the Effectiveness of an Online Behavioral Intervention in Reducing Loneliness
This study will use a longitudinal randomized experimental design. Participants will be randomly assigned to either a positive affect skills intervention or a psychoeducation control group and assessed with questionnaires at baseline and immediately post 8-week intervention.
Participants will be randomly assigned to either a positive affect skills intervention or a
psychoeducation control group, with each intervention lasting 8-weeks. Participants in the
positive affect skills intervention will have full access to the unchanged Happify platform.
The psychoeducation control group participants will use a version of the Happify platform
that encourages thinking about well-being through quizzes and polls without providing any
instructions for promotion (i.e., Wait-list Control). Participants will be asked to complete
questionnaires before and after the 8-week program, at which point study participation will
end.
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