Best Possible Self-Tech for Middle Schoolers

May 18, 2026 updated by: University of Oregon

Promoting Positive Affect and Prosocial Technology Use in Middle Schoolers: A Pilot of the Best Possible Self-Tech Exercise

The goal of this pilot clinical trial is to learn if a single-session writing exercise (i.e., Best Possible Self-Tech) can improve positive affect and prosocial technology use in a community sample of eighth graders. The main questions it aims to answer are:

  1. Can the the Best Possible Self-Tech (BPS-Tech) intervention be feasibly and acceptably delivered in classrooms?
  2. What are the associations between textual features of BPS- Tech entries (e.g., length, vividness, positive tone) and post-intervention positive affect?
  3. How do participants describe their future prosocial online behavior ("doing good"), engagement with prosocial content ("seeing good") and associated positive emotions ("feeling good") in the BPS-Tech writing exercise?

Participants will participate in the BPS-Tech exercise during class time and respond to surveys about their prosocial technology use and positive affect.

Study Overview

Status

Enrolling by invitation

Intervention / Treatment

Detailed Description

Technology use is a central part of adolescent life. A 2024 Pew Research Center Survey showed that 95% of adolescents had access to a smartphone, 88% a desktop or laptop computer, and 83% a gaming console at home. Problematic use of these technology devices impact about 1 in 5 adolescents and can increases the odds of depression, anxiety and stress. However, most adolescents do not exhibit problematic use. To date, the research on technology and mental health has focused primarily on its adverse effects, despite initial evidence that technology can elicit positive affect, learning and social connection.

Adolescents most often use technology to socialize and extend their in-person relationships and are more likely to engage in online pro-social behaviors (e.g., complimenting), than antisocial behavior (e.g., criticism). Moreover, moderate use of technology that is active and social is linked to positive emotions like pleasure or satisfaction. Despite these data, few evidence-based approaches help adolescents mindfully engage with technology in ways that promote well-being and social connection.

The Best Possible Self (BPS) intervention, in which participants envision and write about their best future selves, has been shown to increase positive affect in adults and adolescents. This pilot study will adapt the BPS intervention to focus on positive future technology use (BPS-Tech) and test whether it can be feasibly and acceptably delivered in a middle school classroom. The pilot will also examine the textual features of BPS-Tech written entries (e.g., length, vividness, positive tone) and examine associations with post-intervention positive affect. Finally, the written entries will be analyzed with qualitative methods to describe how adolescents envision prosocial technology use. This study will generate feasibility data for a brief, scalable positive affect intervention and provide new insights into how youth envision using technology for good. Findings will inform refinement of the intervention and lay the groundwork for larger trials designed to prevent problematic technology use and strengthen positive affect during developmentally sensitive periods like adolescence.

Study Type

Interventional

Enrollment (Estimated)

80

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 Locations

    • Oregon
      • Eugene, Oregon, United States, 97403-5237
        • University of Oregon

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. eighth grade student enrolled in a participating middle school
  2. speaks and writes in English
  3. regular access to a web-enabled computer, tablet, or smartphone

Exclusion Criteria:

  1. current participation in psychotherapy for anxiety or depression
  2. a diagnosed cognitive or developmental impairment

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: BPS-Tech
The BPS is a structured writing exercise (i.e., 10 minutes) designed to help individuals imagine the details about their future selves assuming things have gone as well as they possibly could. In the technology-related adaptation, participants are directed to imagine how their best possible self would utilize technology. The goal of the intervention is to increase positive thinking and mindful engagement with technology by helping adolescents envision and articulate optimistic future possibilities for their digital lives.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Program Feedback Scale
Time Frame: Immediately post-intervention
The Program Feedback Scale is a 7-item scale that measures the acceptability of an intervention. The scale was developed specifically for youth participating in single-session interventions. Items are rated on a 5-point Likert scale (range 0-4). Total scores range from 0-28, with higher scores indicating greater acceptability.
Immediately post-intervention
The Positive and Negative Affect Schedule-Child Short Form
Time Frame: Baseline, immediately post-intervention, 1-week follow up, 1 month follow-up
The PANAS-C-SF is a 10-item scale that measures expressed levels of positive and negative affect. Positive affect and negative affect subscale scores range from 5-25, where higher scores indicate higher levels of positive/negative affect.
Baseline, immediately post-intervention, 1-week follow up, 1 month follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prosocial Technology Use
Time Frame: Baseline, 1-week follow up, 1-month follow up
The Tech With Care Index is a 17-item scale that measures the quality of use of digital devices including phones, tablets, laptops, and game consoles among youth. Two subscale scores are calculated by calculating the average (range 1-5) for self-defeating technology use items (i.e., unhealthy or mindless use) and other-benefitting use items (i.e., empathic or civic use). Higher mean scores indicate technology use that is more intentional, mindful and caring.
Baseline, 1-week follow up, 1-month follow up
Digital Flourishing
Time Frame: Baseline, 1-month follow up
The Digital Flourishing Scale is a 25-item scale that measures the strength-based domains of digital technology use including the use of technology for connection, positive social comparison, and meaning making. Total scores range from 25-125, with higher scores indicating more digital flourishing.
Baseline, 1-month follow up

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Teacher-rated Intervention Feasibility
Time Frame: Immediately post-intervention
The Feasibility of Intervention Measure is a 4-item scale that measures the feasibility of implementing an intervention in a particular setting. Items are rated on a 5-point Likert scale (range 1-5). Total scores range from 4-20, with higher scores indicating higher levels of perceived feasibility.
Immediately post-intervention

Collaborators and Investigators

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

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 (Actual)

April 27, 2026

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

September 20, 2026

Study Registration Dates

First Submitted

April 14, 2026

First Submitted That Met QC Criteria

April 14, 2026

First Posted (Actual)

April 20, 2026

Study Record Updates

Last Update Posted (Actual)

May 20, 2026

Last Update Submitted That Met QC Criteria

May 18, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • STUDY00002054
  • 1P50MH139449-01 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All survey and interview data will be de-identified and will be archived in a sharable data repository. Data will uploaded quarterly into the NIMH Data Archive using the NDA Electronic Data Submission Agreement (eDSA) Tool.

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.

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