Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
125 participants
INTERVENTIONAL
2023-08-01
2025-10-18
Brief Summary
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The purpose of this randomized control trial is to investigate the feasibility and efficacy of a Mood Lifters group template specifically for undergraduate students. Mood Lifters is an effective peer-led program that improves or maintains mental health. It seeks to help people enhance pleasure, engagement, and meaning in their lives while minimizing depression, fear, loneliness, and other negative feelings via a proprietary peer-based program that offers weekly meetings and other flexible support options. One obstacle to providing mental health care in the US is that it is costly to provide one-on-one therapy by a licensed professional. This is particularly true in large group settings with limited resources (counseling centers) and a large need for mental health care, like universities.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Treatment Group
Individuals in this arm will take part in the Mood Lifters program immediately after recruitment.
Mood Lifters for Undergraduates
Participants will need to attend 14 hour-long virtual weekly meetings on Zoom that focus on helpful mental health strategies and skills. Participants will be encourage to practice what they learn at home in order to improve their mood or mental wellness.
Waitlist Control Group
Individuals in this arm will be invited to take part in the Mood Lifters program after they complete post-treatment surveys as part of the control group.
No interventions assigned to this group
Interventions
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Mood Lifters for Undergraduates
Participants will need to attend 14 hour-long virtual weekly meetings on Zoom that focus on helpful mental health strategies and skills. Participants will be encourage to practice what they learn at home in order to improve their mood or mental wellness.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* at least 18 years of age
Exclusion Criteria
* active psychosis
* borderline personality disorder
* active mania
* unwillingness to attend all sessions or treatment types (e.g., unwillingness to attend remote)
* non-undergraduate students.
18 Years
ALL
Yes
Sponsors
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University of Michigan
OTHER
Responsible Party
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Patricia Deldin
Principal Investigator
Principal Investigators
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Patricia J Deldin, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University of Michigan
Locations
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University of Michigan
Ann Arbor, Michigan, United States
Countries
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Other Identifiers
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HUM00221612
Identifier Type: -
Identifier Source: org_study_id
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