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Clinical Trials/NCT03072680
NCT03072680
Completed
N/A

Efficacy of a Positive Psychology Intervention Through a Mobile App: a Randomized Controlled Trial

University of Valencia2 sites in 2 countries361 target enrollmentApril 23, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not Flourishing Population
Sponsor
University of Valencia
Enrollment
361
Locations
2
Primary Endpoint
Change of Positive and Negative Affect from baseline to post-intervention
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

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.

Detailed Description

The design will permit two comparisons: After the first week of the intervention, participants will answer the assessment. It will permit to compare BPS PAST, BPS FUTURE and CONTROL conditions (pre-post). After the second week, participants will answer the assessment and then it will be possible to compare BPS PAST + BPS FUTURE combination, BPS FUTURE, and CONTROL conditions.

Registry
clinicaltrials.gov
Start Date
April 23, 2019
End Date
July 27, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rosa María Baños Rivera

Full Professor

University of Valencia

Eligibility Criteria

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)

Outcomes

Primary Outcomes

Change of Positive and Negative Affect from baseline to post-intervention

Time Frame: Change from pre-intervention to post-intervention (2 weeks)

Positive and Negative Affect Scale (PANAS; Watson, Clark \& Tellegen, 1988)

Secondary Outcomes

  • Wellbeing(Change from pre-intervention to post-intervention (2 weeks))
  • Satisfaction with life(Change from pre-intervention to post-intervention (2 weeks))
  • Optimism(Change from pre-intervention to post-intervention (2 weeks))
  • Self-efficacy(Change from pre-intervention to post-intervention (2 weeks))

Study Sites (2)

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