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E-Manage: A Brief mHelath Intervention for University Students

E-Manage: A Brief mHelath Intervention for University Students

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04636151
Enrollment
200
Registered
2020-11-19
Start date
2020-12-04
Completion date
2023-06-30
Last updated
2025-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Distress, Emotional, Suicidal Ideation

Brief summary

This study is a two-part transdiagnostic psychological intervention aimed to help people respond to negative emotion and emotional distress in more adaptive ways using a technology called ecological momentary intervention (or EMI) that delivers intervention content using a smartphone app. Participants in this study will be Rutgers students recruited through-or currently affiliated with - Counseling, Alcohol and Other Drug Assistance Program & Psychiatric Services (CAPS) at Rutgers. Participants will first attend either one-on-one or group telehealth therapy sessions/workshops, where they will learn the therapeutic skills that are part of the study. Then, they will complete up to 8 weeks of smartphone monitoring that involves assessments and opportunities to practice the skills learned in therapy.

Interventions

Content of this intervention is based on pre-established transdiagnostic protocols for addressing the negative emotion associated with suicidal thoughts and behaviors.

Sponsors

Massachusetts General Hospital
CollaboratorOTHER
Rutgers, The State University of New Jersey
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 years or older * Matriculated at Rutgers during Fall of 2020 (on campus and/or remote) * Currently residing in US * Willingness to follow study requirements, as evidenced by an ability to provide written informed consent and read, understand, and complete the study procedures * iOS and Android smartphone compatible with MetricWire. Nearly all phones since 2014 are compatible

Exclusion criteria

* Non-English speaking * Unable to understand or provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Change in momentary levels of self-reported distress8 week study periodAssessed via smartphone assessments

Secondary

MeasureTime frameDescription
Change in momentary levels of suicidal thinking8 week study periodAssessed via smartphone assessments

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026