Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05651295

A Precision Medicine Approach to Target Engagement for Emotion Regulation

Led by Matthew Southward, PhD · Updated on 2026-05-11

390

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

M

Matthew Southward, PhD

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating whether teaching people personalized versus standardized emotion regulation skills can better reduce daily negative emotions. The study also aims to see if matching participants to their predicted best skill training is feasible and helpful. This research may reveal how emotion regulation treatments impact emotional health and help develop personalized, evidence-based, and scalable interventions. Participants will be randomly assigned to learn one of three emotion regulation skills—cognitive restructuring, opposite to emotion action, or mindfulness—that matches their personal strengths, or to learn all three skills through interactive videos with surveys to practice and check understanding. These training conditions are designed to compare focused versus broad skill coverage. During the study, participants will report their emotions multiple times daily for 42 days, using the Positive and Negative Affect Schedule-Short Form. They will also complete assessments every two weeks for six weeks, measuring depression, anxiety, personality traits, responses to emotions, and breath-counting tasks. Researchers will monitor changes in emotion regulation effectiveness and emotional experiences to understand the impact of the training.

CONDITIONS

Brief Title

A Precision Medicine Approach to Target Engagement for Emotion Regulation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Elevated emotion dysregulation
Not Eligible

You will not qualify if you...

  • Lack of proficiency in English
  • No access to smartphone
  • Conditions requiring greater than outpatient care

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants learn emotion regulation skills through interactive videos and complete related surveys to practice and understand the skills.

Multiple video sessions over 6 weeks

Monitoring

Duration - 42 to 48 days

Participants provide frequent self-reports on affect and emotion regulation effectiveness using surveys throughout the study period.

7 times daily self-reporting

Trial Site Locations

Total: 1 location

1

Ohio State University

Columbus, Ohio, United States, 43210

Actively Recruiting

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Research Team

M

Matthew W Southward, Ph.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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