Efficacy of a Positive Psychology Intervention Through a Mobile App
Launched by UNIVERSITY OF VALENCIA · Mar 2, 2017
Trial Information
Current as of May 23, 2025
Completed
Keywords
ClinConnect Summary
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.
Gender
ALL
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)
About University Of Valencia
The University of Valencia, a prestigious institution located in Spain, is dedicated to advancing scientific knowledge and improving public health through innovative research. With a strong emphasis on interdisciplinary collaboration, the university engages in a wide array of clinical trials aimed at addressing pressing medical challenges. Its commitment to ethical standards and regulatory compliance ensures the integrity of its research initiatives, while its experienced team of researchers and clinicians work diligently to translate scientific discoveries into practical applications that benefit patients and communities. The University of Valencia is at the forefront of medical research, fostering a culture of excellence and innovation in the pursuit of better healthcare solutions.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Valencia, , Spain
Enschede, Overijssel, Netherlands
Patients applied
Trial Officials
Rosa Baños, PhD
Principal Investigator
University of Valencia
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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