PERMA-Based Mobile Psychological Intervention With and Without Telephone Support for University Students

March 6, 2026 updated by: Vanessa Blanco Seoane, University of Santiago de Compostela

Efficacy of a Positive Psychology-Based Psychological Intervention Grounded in the PERMA Model Delivered Via Smartphone App, With and Without Telephone Multiconference Support, for the Promotion of Psychological Well-Being in University Students

University students face increasing academic and psychosocial demands that place them at risk of reduced psychological well-being. Positive psychology interventions have demonstrated efficacy in promoting mental health; however, few are grounded explicitly in Seligman's PERMA model and adherence to digital interventions remains limited. This randomized controlled trial aims to evaluate the efficacy of a brief PERMA-based psychological intervention delivered via a smartphone application, with and without supplementary telephone multiconference support, compared to a waiting list control group. The intervention consists of five weekly modules targeting Positive Emotion, Engagement, Relationships, Meaning, and Accomplishment. Assessments will be conducted at baseline, post-intervention, and at six-month follow-up.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

177

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Being an actively enrolled university student at the University of Santiago de Compostela (USC)
  • Having access to a smartphone with an internet connection.

Exclusion Criteria:

  • Having a current diagnosis of severe psychiatric disorder, including major depressive disorder with psychotic features, bipolar disorder, schizophrenia, severe cognitive impairment, dissociative disorders, or active substance dependence
  • Having started psychological or psychopharmacological treatment within the two months prior to the study or participating in another mental health-related study
  • Having insufficient proficiency in Spanish, or presenting sensory, cognitive, or physical impairments that would prevent engagement with the intervention
  • Planning to move out of Galicia within the next 12 months.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: App-based PERMA intervention (PPIA)
Behavioral intervention delivered via smartphone app. Five weekly modules corresponding to the PERMA domains.
The PPIA intervention is a structured psychological program grounded in the PERMA model of well-being (Seligman, 2011). This model proposes that long-term flourishing depends on developing five pillars: Positive Emotion, Engagement, Relationships, Meaning, and Accomplishment. The intervention is further supported by the broaden-and-build theory of positive emotions (Fredrickson, 2001), flow theory (Csikszentmihalyi, 1990), research on character strengths and positive relationships (Peterson & Seligman, 2004; Reis & Gable, 2003), meaning in life (Steger, 2009), the goal-setting theory (Locke & Latham, 2002) and growth mindset principles (Dweck, 2006).
Experimental: App-based PERMA intervention plus telephone multiconference (PPIA+M)
Same app-based intervention supplemented by weekly 30-minute group telephone multiconference sessions.
The PPIA intervention is a structured psychological program grounded in the PERMA model of well-being (Seligman, 2011). This model proposes that long-term flourishing depends on developing five pillars: Positive Emotion, Engagement, Relationships, Meaning, and Accomplishment. The intervention is further supported by the broaden-and-build theory of positive emotions (Fredrickson, 2001), flow theory (Csikszentmihalyi,1990), research on character strengths and positive relationships (Peterson & Seligman, 2004; Reis & Gable, 2003), meaning in life (Steger, 2009), the goalsetting theory (Locke & Latham, 2002) and growth mindset principles (Dweck, 2006). Additionally, the multiconference component will consist of weekly 30-minute telephone-based multiconference sessions. During these sessions, positive or corrective feedback will be delivered in accordance with Miltenberger's guidelines (Miltenberger, 2012) after reviewing the completed homework.
No Intervention: Waiting List Control Group (WLCG)
Participants receive no intervention during the study period and are granted access after completion.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline emotional well-being to post-intervention (5 weeks) and 6-month follow-up
Time Frame: Pre- and post -intervention (5 weeks) and 6-month follow-up
One of the primary outcomes of the study will be emotional well-being. This construct will be evaluated using the Warwick-Edinburgh Mental Well-Being Scale (WEMWBS; Tennant et al., 2007).
Pre- and post -intervention (5 weeks) and 6-month follow-up
Change from baseline well-being to post-intervention (5 weeks) and 6-month follow-up
Time Frame: Pre- and post -intervention (5 weeks) and 6-month follow-up.
One of the primary outcomes of this study will be well-being (which comprises three elements, emotional, psychological and social well-being)l. This constructs will be evaluated using the Mental Health Continuum-Short Form (MHC-SF; Keyes, 2002).
Pre- and post -intervention (5 weeks) and 6-month follow-up.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

August 31, 2029

Study Completion (Estimated)

August 31, 2029

Study Registration Dates

First Submitted

February 27, 2026

First Submitted That Met QC Criteria

March 6, 2026

First Posted (Actual)

March 12, 2026

Study Record Updates

Last Update Posted (Actual)

March 12, 2026

Last Update Submitted That Met QC Criteria

March 6, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • USC-003/2026-H

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Researchers will report study results through publications. The data supporting these findings will be presented in the main publications, and the datasets used during the study can be obtained from the corresponding author on reasonable request.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Psychological Well Being

Clinical Trials on App Based PERMA intervention

Subscribe