Skip to main content
Clinical Trials/NCT03378505
NCT03378505CompletedNot Applicable

Living Purposefully: The Role of Mobile App JOOL in Promoting Well-being and Academic Success

University of Wisconsin, Madison1 site in 1 country112 target enrollmentStarted: January 24, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
112
Locations
1
Primary Endpoint
Change in Resiliency

Study Overview

Brief Summary

This study will examine the impact of a mobile app (JOOL) focused on promoting purposeful living on student health behaviors, academic performance, self-regulation, well-being, resiliency, and self-efficacy.

Detailed Description

Participants will be recruited from a large undergraduate classroom. Participants will be randomly assigned to one of two conditions and asked to complete either online reflections or engage with a mobile app over the course of the semester. Students who elect to not participate will be provided an alternate assignment to complete, to be coordinated by their teaching assistant. Participants will additionally be asked to complete (1) a pre-survey, (2) post-survey, and follow-up survey 14 days after the class concludes. The study will examine changes in health-related behaviors, resiliency, well-being, and self-efficacy reported between the start and conclusion of semester/study.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Minimum age of 18 years
  • •Enrolled in Consuming Happiness course during the Spring 2017-18 semester.
  • •Must have access to WiFi, cellular service or computer with internet connection and web browser.

Exclusion Criteria

  • Not provided

Arms & Interventions

Mobile App

Experimental

Half of the students randomly assigned

Intervention: Mobile App (Behavioral)

Reflection

Experimental

Half of the students randomly assigned

Intervention: Reflection (Behavioral)

Outcomes

Primary Outcomes

Change in Resiliency

Time Frame: 14 weeks post start (1 semester)

Brief Resiliency Scale (BRS) used to measure resiliency, or ""the ability to bounce back or recover from stress" (Smith et al., 2008). 6 items using Likert scale strongly disagree (1) to strongly agree (5). Score will be summed for one total score and can range from 6 to 30, with 6 indicating low resilience and 30 indicating high resilience. No clinical cut off. Expected increase no change in scores from pre and post.

Change in Well-Being

Time Frame: 14 weeks post start (1 semester)

The WHO (Five) Well-Being Index (WHO-5) measures well-being, defined as the subjective quality of life based on positive mood (good spirits, relaxation), vitality (being active and waking up fresh and rested), and general interest (being interested in things). 5 items on a Likert scale ranging from all of the time (5) to at no time (1). Responses will be summed for one total score ranging from 0 to 25. 0 indicates low well-being and 5 indicates high well-being. Score below 13 indicates poor well-being. Expected increase or no change in scores from pre and post.

Change in Health Behaviors

Time Frame: 14 weeks post start (1 semester)

Expected increase in self-report of behaviors promoting academic achievement, physical health, well-being, and purpose from time of pre survey to post survey.

Change in belief of ability to perform difficult tasks or cope with diversity

Time Frame: 14 weeks post start (1 semester)

Generalized Self-Efficacy Scale used to measure self-efficacy, or "the optimistic self-belief that one can perform novel or difficult tasks or cope with diversity" (Schwarzer, 1992). 10 items on a Likert scale from Not true at all (1) to Exactly true (4). Responses will be summed for one total score, ranging from 10 to 40. 10 indicates low self-efficacy, 40 indicates high self-efficacy. No clinical cut off. Expected increase or no change in scores from pre and post.

Change in Self-Regulation

Time Frame: 14 weeks post start (1 semester)

Self-Regulation Scale (SRQ) short form used to measure self-regulation, or ""the ability to develop, implement, and flexibly maintain planned behavior in order to achieve one's goal" (Brown, Miller, \& Lawendowski, 1999). 31 items using a Likert scale strongly disagree (1) to strongly agree (5), with 14 reverse coded. Scores will be summed for one total score ranging from 31 to 155. 31 indicates low self-regulation and 155 indicates high self-regulation. No clinical cut off. Expected increase or no change in scores from pre and post.

Secondary Outcomes

  • Change in Health Behaviors(14 days (2 weeks) after end of study (16 weeks post start))
  • App Perceptions(14 days (2 weeks) after end of study (16 weeks post start))

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials