Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07350733

Cognitive Training for Student Sleep and Wellness

Led by Carnegie Mellon University · Updated on 2026-04-02

200

Participants Needed

4

Research Sites

15 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized control trial (RCT) explores two potential stress reduction interventions: a digital mindfulness program personalized for first year college students and a problem-solving based stress management program. These interventions were chosen because they rely on evidence-based approaches to stress management: problem-solving for cognitive coping and mindfulness for attention monitoring and acceptance with a focus on concentration, clarity, and equanimity. This selection allows for the assessment of the comparative efficacy of these methods in addressing student stress and stress-related outcomes (sleep duration, mental health, and academic success). Personalization to the college student offers the potential for greater engagement and user satisfaction by tailoring the program while maintaining the empirically driven structure of a digital mindfulness program. The investigators predict greater engagement and satisfaction will lead to higher adherence, and thus more skill-building. In this small RCT, first year college students will complete one of the two intervention conditions: Equa and MyTime. This will allow for the exploration of the effects of personalized mindfulness training compared to an active control condition. This work has the potential for identifying effective, low-cost tools to help young adults manage their stress and stress-related health and may inform theory and future work on stress modification strategies for other populations. The main trials aims are: Specific Aim 1. To explore whether a personalized mindfulness intervention (Equa) leads to greater adherence, engagement and use satisfaction compared to a digital stress management program. Specific Aim 2. To explore whether a personalized mindfulness intervention leads to greater improvements in student stress and stress-related outcomes compared to a problem solving-based digital stress management program. Outcomes include perceived stress, depressive symptoms, nightly sleep duration, and grades.

CONDITIONS

Official Title

Cognitive Training for Student Sleep and Wellness

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be a first-year undergraduate student at Carnegie Mellon University, University of Notre Dame, Columbia University, or Pennsylvania State University
  • Be 18 years of age or older
  • Have a data-enabled smartphone
  • Speak English
  • Be on campus for the entire Spring 2026 semester
Not Eligible

You will not qualify if you...

  • Be under 18 years of age at time of enrollment
  • Not be enrolled full-time as a student

AI-Screening

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Trial Site Locations

Total: 4 locations

1

University of Notre Dame

Notre Dame, Indiana, United States, 46556

Actively Recruiting

2

Columbia University

New York, New York, United States, 10027

Actively Recruiting

3

Carnegie Mellon University

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

4

Pennsylvania State University

University Park, Pennsylvania, United States, 16802

Actively Recruiting

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Research Team

S

Sarah Wu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Cognitive Training for Student Sleep and Wellness | DecenTrialz