Not Flourishing Population Clinical Trial
Official title:
Efficacy of a Positive Psychology Intervention Through a Mobile App: a Randomized Controlled Trial
| NCT number | NCT03072680 |
| Other study ID # | 16337 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | April 23, 2019 |
| Est. completion date | July 27, 2019 |
| Verified date | September 2019 |
| Source | University of Valencia |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The aim of this study is to analyze the efficacy of several variations of an already
validated Positive Psychology Intervention (PPI) called Best Possible Self in not flourishing
population. This will be done through a mobile app specially designed for this aim.
Concretely, the design will permit to compare the classic intervention (BPS Future), a new
variation (BPS Past), and a combination of both components (BPS Past+Future).
Participants will be randomly assigned to one of 3 conditions, in which they will practice
the intervention for two weeks:
- BPS-PAST + BPS FUT condition: Participants will practice BPS Past for one week, and then
they will switch to BPS future for another week.
- BPS-FUT condition: Participants will practice BPS Future for two weeks.
- CONTROL condition: Participants will practice DAILY ACTIVITIES for two weeks.
| Status | Completed |
| Enrollment | 361 |
| Est. completion date | July 27, 2019 |
| Est. primary completion date | July 27, 2019 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Participants must be 18 years old or older. - Participants must be willing to participate in the study. - Participants must have a smartphone (Android or Ios). Exclusion Criteria: - To suffer from moderate depression or anxiety (scores of 11 or higher) measured by the Hospital Anxiety and Depression Scale (HADS; Zigmond & Snaith, 1983). - To have "Flourishing mental health" measured by the Mental Health Continuum Short Form (MHC-SF; Keyes, 2009) |
| Country | Name | City | State |
|---|---|---|---|
| Netherlands | University of Twente | Enschede | Overijssel |
| Spain | University of Valencia | Valencia |
| Lead Sponsor | Collaborator |
|---|---|
| University of Valencia | University of Twente |
Netherlands, Spain,
King L. The Health Benefits of Writing About Life Goals. Personality and Social Psychology Bulletin 27(7): 798-807, 2001.
Meevissen YM, Peters ML, Alberts HJ. Become more optimistic by imagining a best possible self: effects of a two week intervention. J Behav Ther Exp Psychiatry. 2011 Sep;42(3):371-8. doi: 10.1016/j.jbtep.2011.02.012. Epub 2011 Mar 2. — View Citation
Peters ML, Flink IK, Boersma K, Linton SJ. Manipulating optimism: Can imagining a best possible self be used to increase positive future expectancies? The Journal of Positive Psychology 5(3): 204-211, 2010.
Sheldon KM, Lyubomirsky S. How to increase and sustain positive emotion: The effects of expressing gratitude and visualizing best possible selves. The Journal of Positive Psychology 1(2): 73-82, 2006.
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change of Positive and Negative Affect from baseline to post-intervention | Positive and Negative Affect Scale (PANAS; Watson, Clark & Tellegen, 1988) | Change from pre-intervention to post-intervention (2 weeks) | |
| Secondary | Wellbeing | The Mental Health Continuum Short Form (MHC-SF; Keyes, 2009) | Change from pre-intervention to post-intervention (2 weeks) | |
| Secondary | Optimism | Life Orientation Test (LOT-R; Scheier, Carver & Bridges, 1994). | Change from pre-intervention to post-intervention (2 weeks) | |
| Secondary | Satisfaction with life | Temporal Satisfaction with Life Scale (TSWLS; Pavot, Diener & Suh, 1998). | Change from pre-intervention to post-intervention (2 weeks) | |
| Secondary | Self-efficacy | New General Self-efficacy Scale (NGSES; Chen, Gully & Eden, 2001). | Change from pre-intervention to post-intervention (2 weeks) |