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College Student Stress: Transitions Over Time

Not Applicable
Completed
Conditions
Depressive Symptoms
Registration Number
NCT06583096
Lead Sponsor
University of Michigan
Brief Summary

This research study is being conducted to better understand how college students develop and cope with stress and to identify opportunities to help students notice and respond to stress early before symptoms contribute to significant negative consequences.

This project will be completed in two parts. In the first part (not a trial) participants will be asked to complete a screening survey to determine eligibility. Eligible participants (i.e., those with mild-to-moderate depressive symptoms and not receiving mental health care) will continue into the clinical trial portion (part two). There were 120 students in the clinical trial phase of the study, where 30 were randomly assigned to "assessment only" and 90 to the "intervention" condition.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
120
Inclusion Criteria
  • First-year college students that are full-time or part-time students enrolled at the University of Michigan, Ann Arbor or Flint campuses
  • Mild-to-moderate depressive symptoms, and are not receiving professional mental health services will be eligible
Exclusion Criteria
  • Under the age of 17
  • Currently be receiving mental health therapy/counseling from a healthcare professional
  • Experiencing minimal depressive symptoms (defined in protocol)
  • Experiencing moderately severe to severe depressive symptoms (defined in protocol)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Percentage of eligible participants that agree to participate in the trial10-20 days after screen survey
Percentage of completed follow-upsBaseline up to six-week follow-up
Percentage of participants that remain active (i.e. do not request to stop messages) on the text-message groupBaseline up to six-week follow-up
Number of withdrawalsBaseline up to six-week follow-up
Total percent of feedback reports that were viewed across all sent feedback reportsBaseline up to six-week follow-up
Percent of participants (in the intervention arm) that viewed a personalized feedback report at least onceBaseline up to six-week follow-up
Participant self-reported satisfaction with the intervention componentsSix-week follow-up

There are 8 questions regarding satisfaction (1-Strongly disagree, 4 Neither agree nor disagree, 7-Strongly Agree) that the participant will complete regarding the study. Additionally, two questions will be open ended to collect information about the study. A higher score means more satisfaction with the study.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Michigan

🇺🇸

Ann Arbor, Michigan, United States

University of Michigan
🇺🇸Ann Arbor, Michigan, United States

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