Depression, happiness, affect, personal satisfaction, emotions, health promotion
Conditions
Interventions
The registration of the participants and completion of the scales and daily lists will be done through the Survey Monkey online questionnaire tool. The scales that will be applied are: Positive and Ne
Behavioural
V03.175.250
Sponsors
Universidade Federal de Ciências da Saúde de Porto Alegre
Universidade Federal de Ciências da Saúde de Porto Alegre
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Adult volunteers; minimum age of 18; both genders; active email account
Exclusion criteria
Exclusion criteria: Age less than 18 years; inactive email account; failure to complete the initial scales of the study and the sociodemographic questionnaire
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increase in the happiness score, assessed through the Subjective Happiness Scale, with a statistically significant pre and post-test difference (significance level considered 5%). Data collected before the intervention, at the end of the intervention (lasting 2 weeks) and 2 weeks after the intervention.;Increase in the life satisfaction score, evaluated through the Life Satisfaction Scale, with a statistically significant pre and post-test difference (significance level considered 5%). Data collected before the intervention, at the end of the intervention (lasting 2 weeks) and 2 weeks after the intervention.;Increase in the positive affect score, evaluated through the Affect Scale, with a statistically significant pre and post-test difference (significance level considered 5%). Data collected before the intervention, at the end of the intervention (lasting 2 weeks) and 2 weeks after the intervention.;Decrease in the negative affect score, evaluated through the Affect Scale, with a statistically significant pre and post-test difference (significance level considered 5%). Data collected before the intervention, at the end of the intervention (lasting 2 weeks) and 2 weeks after the intervention.;Decrease in the depressive symptom score, assessed through the Center for Epidemiological Studies Depression Scale, with a statistically significant pre and post-test difference (significance level considered 5%). Data collected before the intervention, at the end of the intervention (lasting 2 weeks) and 2 weeks after the intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Public ContactCaroline Reppold
Universidade Federal de Ciências da Saúde de Porto Alegre
Outcome results
None listed