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Not yet recruitingNCT07926919Updated Nov 9, 2026

Beary's GEM Project: Emotion Regulation Flexibility Among College Students

An interventional study of Beary's GEM project and Sharing Feelings Project in Emotion Regulation Flexibility, sponsored by University of California, Irvine. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-09.

Sponsored by University of California, Irvine · Not applicable, Interventional, and Supportive care

Updated Nov 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
700
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to evaluate a single-session intervention program on emotion regulation flexibility in college students. The main questions it aims to answer are:

  • To evaluate the effectiveness of the digital single-session intervention program in improving emotion regulation flexibility among college students.
  • To examine the effectiveness of the intervention in supporting well-being, including psychological distress and subjective well-being.
  • To examine the acceptability and utility of the emotion regulation flexibility single-session intervention program.
  • To explore participants' personal understanding of emotion regulation flexibility and the experience of intervention through semi-structured interviews.

Researchers will compare the experimental group (Beary's GEM program) and the active control group (Sharing Feelings Project) to answer the first two research questions.

Participants will

  • Be randomly assigned and complete a digital single-session intervention
  • Complete pre- and post-intervention questionnaires on emotion regulation flexibility and well-being
  • Have a video chat with a researcher (optional)
02

Conditions studied

  • Emotion Regulation Flexibility

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Keywords

  • Emotion Regulation Flexibility
  • College Students
  • Single-session Intervention
03

In context

Emotional Regulation

545 studies on the registry are indexed under Emotional Regulation; 188 are open to participants now.

This study's planned enrollment of 700 is above the median of 79 across 498 interventional studies indexed under Emotional Regulation.

Browse Emotional Regulation studies →

Lead sponsor

University of California, Irvine is the lead sponsor of 476 studies on the registry; 98 are open to participants now.

Of its 41 completed or terminated interventional studies of FDA-regulated products, 30 (73%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age: >=18 and \<=25 as of 2026 November
  • To be assigned to the experimental group or the waitlist control group, participants who score below the median (ERFS \<= 33) on the 9-item Emotion Regulation Flexibility Scale will be redirected and randomly assigned to a study condition. This decision was made based on a previous study on the emotion regulation flexibility intervention to reduce the ceiling effect. However, all the questionnaire responses (regardless of scores on ERFS) for assessment 1 will be maintained.
  • Able to comprehend and complete the questionnaire and intervention in English

Exclusion criteria

Exclusion Criteria:

  • Not within the target age range
  • Participants who had a score greater than 33 on the 9-item Emotion Regulation Flexibility Scale will not be assigned to a study condition after completing assessment 1.
  • Not able to comprehend and complete the questionnaire in English
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
700 participants (estimated)

Study arms

  • Experimental
    Beary's GEM Project

    Participants will complete a series of brief, structured activities that are designed to introduce and practice emotion regulation strategies and their flexibility.

    Behavioral: Beary's GEM project

  • Active comparator
    Sharing Feelings Project

    The Sharing Feeling Project will be administered as the placebo intervention for the active control group. This condition focuses on content that encourages participants to share feelings with people in their support circle.

    Behavioral: Sharing Feelings Project

Interventions

  • BehavioralBeary's GEM project

    Participants in the experimental group will be directed to a digital, single-session intervention (Beary's GEM Project) that targets three aspects of emotion regulation flexibility: context sensitivity, repertoire, and feedback responsiveness.

  • BehavioralSharing Feelings Project

    Participants in the active control group will be directed to a digital single-session intervention (Sharing Feelings Project) aiming to encourage participants to share feelings with people in their support circle. However, unlike the experimental intervention, it does not teach a specific psychological mechanism (i.e., emotion regulation flexibility).

06

What researchers measure

Primary outcomes

  1. Emotion Regulation Flexibility

    12 indicates the lowest emotion regulation flexibility, and 60 indicates the highest.

    Time frame: Baseline, post-intervention (around 1 week after baseline), 1-week follow-up, and 2-week follow-up

  2. Depression, Anxiety & Stress

    0 indicates the lowest psychological distress, and 126 indicates the highest.

    Time frame: Baseline, 1-week follow-up, and 2-week follow-up

  3. Resilience

    6 indicates the lowest resilience, and 30 indicates the highest.

    Time frame: Baseline, 1-week follow-up, and 2-week follow-up

  4. Program Feedback

    0 indicates the lowest user experience, and 28 indicates the highest.

    Time frame: Post-intervention (around 1 week after baseline)

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Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Lovibond PF, Lovibond SH. The structure of negative emotional states: comparison of the Depression Anxiety Stress Scales (DASS) with the Beck Depression and Anxiety Inventories. Behav Res Ther. 1995 Mar;33(3):335-43. doi: 10.1016/0005-7967(94)00075-u. PubMed 7726811 ↗
  • Smith BW, Dalen J, Wiggins K, Tooley E, Christopher P, Bernard J. The brief resilience scale: assessing the ability to bounce back. Int J Behav Med. 2008;15(3):194-200. doi: 10.1080/10705500802222972. PubMed 18696313 ↗
  • Schleider JL, Mullarkey MC, Weisz JR. Virtual Reality and Web-Based Growth Mindset Interventions for Adolescent Depression: Protocol for a Three-Arm Randomized Trial. JMIR Res Protoc. 2019 Jul 9;8(7):e13368. doi: 10.2196/13368. PubMed 31290406 ↗
  • Schleider JL, Abel MR, Weisz JR. Do Immediate Gains Predict Long-Term Symptom Change? Findings from a Randomized Trial of a Single-Session Intervention for Youth Anxiety and Depression. Child Psychiatry Hum Dev. 2019 Oct;50(5):868-881. doi: 10.1007/s10578-019-00889-2. PubMed 30993499 ↗
  • Sharma P, Singh P. Translating theoretical insights into an emotion regulation flexibility intervention: assessing effectiveness. Cogn Emot. 2025 Mar;39(2):355-376. doi: 10.1080/02699931.2024.2413366. Epub 2024 Oct 10. PubMed 39387144 ↗

Individual participant data

Plan to share: Yes — All of the de-identified data collected in this research will be maintained and possibly shared, including (but not limited to questionnaire responses and electronic files containing coded data.

Supporting information: Analytic code

Access criteria: De-identified data will be made available to researchers unassociated with the UCI study team upon reasonable request, as determined by the lead researcher of this protocol. De-identified data will also be made available on the Open Science Framework or similar sites in accordance with journal requirements for the purposes of transparency in scientific practices. Identifiable information will not be shared.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Nov 9, 2026
Show all 1 update
  1. Nov 9, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07926919
Responsible party
Wenqi Zhang (Graduate Student, University of California, Irvine) — Principal investigator
First posted
Nov 9, 2026
Start date
Nov 2026 (estimated)
Primary completion
Mar 2027 (estimated)
Completion
May 2027 (estimated)
Last update
Nov 9, 2026

Study contacts

Wenqi Zhang
Contact
wenqiz11@uci.edu
413-552-9158

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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