Purpose

The purpose of this research study is to provide a free 6-week, online psychological coaching program to NSU undergraduate students to help with anxiety, depression, and stress, while improving quality of life and healthy coping skills.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Currently matriculating NSU undergraduate students (ages 18+)

Exclusion Criteria

  • Students who are not current NSU undergrads, participants aged 17 and younger, students who are currently enrolled in psychotherapy or mental health services, or students with acute mental health needs (e.g., psychosis, active alcohol or substance use problems, suicidality)

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover Assignment
Primary Purpose
Supportive Care
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Intervention Group
The coaching program will consist of (6) free, 60 minute online coaching sessions. You will be assigned the same coach for the 6 weeks. You can coordinate schedule day/time preferences as the sessions will be done through HIPAA Zoom. Everyone in the study will get the same coaching topics in the same order.
  • Behavioral: online mental health coaching
    SWAG-R Program: A 6-week Coaching Program Designed for NSU Undergraduate Students to Decrease Anxiety, Depression, and Stress and Improve Mental Health, Quality of Life, and Resiliency
    Other names:
    • SWAG-R Coaching Program
No Intervention
Waitlist Group
Waitlist, no intervention group

Recruiting Locations

More Details

Status
Recruiting
Sponsor
Nova Southeastern University

Study Contact

Principal Investigator
954-262-5880
kthayer@nova.edu

Detailed Description

- All study participants will first complete a study pre-screen over the phone with a study team member. This screening will take 10-15 minutes. - If participants are eligible to participate in the study, participants will be verbally guided through the Informed Consent form to determine if participants have any questions. This phone call will take approximately 10 minutes. - Participants will then be electronically sent the Informed Consent form for participant review and to complete and sign, if participants would like to participate in the study. - Once investigators receive the signed Informed Consent document, participants will be assigned a unique Study Identification Number and first assessment measures will be sent to complete (Time Point 1). This assessment will be completed electronically at participant convenience. - Participants will then be randomly assigned to either start the free 6-week online coaching program OR will be randomly assigned to the waitlist for 6 weeks. Participants have an equal chance of being offered the coaching program right away or being put on the waitlist. - The coaching program will consist of (6) free, 60 minute online coaching sessions. Participants will be assigned the same coach for the 6 weeks. Participants can coordinate schedule day/time preferences as the sessions will be done through HIPAA Zoom. Everyone in the study will get the same coaching topics in the same order. - 6 weeks later, participants will complete another assessment (Time Point 2). This assessment will be completed electronically at participant convenience. - If participants were on the waitlist, these participants can now start the free 6 week online coaching program, if participants would like. Participants are not obligated to participate but will be offered the program. - If participants already completed the 6 week online coaching program, participants will not have any other coaching sessions during this time. - 6 weeks later, participants will complete another assessment (Time Point 3). This assessment will be completed electronically at participant convenience. - 6 weeks later, participants will complete another assessment (Time Point 4). This assessment will be completed electronically at participant convenience.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.