About this trial
This study evaluates the feasibility, acceptability, and preliminary efficacy of a brief email-delivered positive affect intervention for young adults in Zimbabwe. The study uses a randomised controlled trial design with two parallel arms.
A total of 100 participants aged 18-25 years will be randomly assigned to two arms: an experimental arm receiving an email-delivered positive affect intervention or a control arm receiving psychoeducational materials. The intervention group will receive guided activities twice weekly over three weeks, focusing on identifying, reflecting on, and engaging in positive experiences. The control group will receive general psychoeducational materials on mental health without structured activities.
Assessments will be conducted at baseline and after the intervention. The primary outcome is feasibility( including recruitment, retention, and adherence) and acceptance. Secondary outcomes include changes in positive affect, symptoms of depression and anxiety,self-stigma, and suicidal ideation.
Eligibility criteria
Qualifiers
Aged 18-25 years.
Able to understand and read English.
Previously participated in Stage 1 of the study and provided consent to be contacted regarding future research opportunities.
Have access to a device (for example smartphone, tablet, or computer) and internet connectivity for intervention delivery.
Disqualifiers
Are at high risk of suicide.
Are currently experiencing a psychotic episode.
Are currently experiencing interpersonal violence.
Trial design
Treatments tested in this trial
- Email-Delivered Positive Affect Intervention
- Psychoeducational Control
Treatment groups
Sponsors and collaborators
Vilnius University
Lead sponsor
University of Zimbabwe
Collaborator