Mode
Text Size
Log in / Sign up
N/A N=21 Supportive Care

IntelliCare in College Students

Depression · Anxiety

Enrolled (actual)
21
Serious AEs
0.0%
Results posted
Oct 2020
Primary outcome: Primary: Patient Health Questionnaire - 8 (PHQ-8) - Depression Severity Module — 2.43; 9.28 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Mobile self-help intervention (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Northwestern University
Primary completion
Nov 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Patient Health Questionnaire - 8 (PHQ-8) - Depression Severity Module
0.6; 9
PRIMARY
Patient Health Questionnaire - 8 (PHQ-8) - Depression Severity Module
0.6; 9
PRIMARY
GAD-7 (Generalized Anxiety Disorder Scale-7)
2.86; 10
PRIMARY
GAD-7 (Generalized Anxiety Disorder Scale-7)
2.86; 10
PRIMARY
Anxiety Literacy Questionnaire
14.63
PRIMARY
Anxiety Literacy Questionnaire
14.63
PRIMARY
Depression Literacy Questionnaire
14.68
PRIMARY
Depression Literacy Questionnaire
14.68
PRIMARY
Cognitive and Behavioral Response to Stress Scale
12.22; 11.55; 19.22; 15.72
PRIMARY
The Cognitive and Behavioral Response to Stress Scale
12.58; 12.68; 19.68; 16.52
SECONDARY
Mean Number of Treatment App Use Sessions
17.05

Summary

This study is an 8-week usability and feasibility trial of the smartphone student stress-management app IntelliCare for college students. This intervention will be tested with University of Illinois at Chicago (UIC) and Northern Illinois University (NIU) students. During this period, research surveys assessing depression and anxiety can be completed on the app. Also, user feedback interviews will be conducted viatelephone at four weeks and at eight weeks to gain insight on the user experience of IntelliCare for College Students.

Eligibility Criteria

Inclusion Criteria

Participant is a student at the University of Illinois in Chicago or Northern Illinois University. Participant owns a smartphone capable of running Android 7 (or higher) or iOS11 (or higher).

Participant is 18 years of age or older

Exclusion Criteria

None

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04035577). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search