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From Intention to Action:Scoring Your College Goals

Primary Purpose

Depression, Anxiety

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Scoring Your College Goals Workshop
Placebo
Sponsored by
The Zucker Hillside Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Depression focused on measuring Depression, Anxiety, College Mental Health, Mental Health Prevention

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • First-year, first semester freshman enrolled in Psychology 100 courses at CUNY College of Staten Island.

Exclusion Criteria:

  • Under 18 years old
  • Violation of inclusion criteria

Sites / Locations

  • CUNY College of State Island

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

College Workshop Arm

Placebo

Arm Description

Intervention

Placebo

Outcomes

Primary Outcome Measures

Change in Self-Reported Depression Symptoms on the DASS-21
Change in Depression Symptoms as measured by self-report on the Depression sub scale of the Depression, Anxiety and Stress Scale (DASS-21). Each sub scale of the DASS-21 has a range of 0-(lowest) to 42 (highest) with higher scores indicating worsening levels of psychopathology.
Change in Anxiety Symptoms as measured by the DASS-21
Participants in the intervention arm but not the placebo group will demonstrate change in Depression Symptoms as measured by participant self-report on the Anxiety subscale of the Depression, Anxiety and Stress Scale (DASS-21).

Secondary Outcome Measures

Change in self-efficacy as measured by the Coping Self-Efficacy Scale
Participants in the intervention group but not the control group will demonstrate significant change in self-reported self-efficacy scores as measured by the Coping Self-Efficacy Scale (CSE). Each sub scale of the CSE has a range of scores from 0 (lowest) to 60 (highest) with a higher score representing better (improved) coping self-efficacy.
Change in Coping abilities as measured by the Brief COPE
Participants in the intervention group but not the control group will demonstrate significant change in their ability to cope with stress as measured by self-reported total scores on the Brief COPE. The fourteen sub scales of the Brief COPE each have a range of 0 (lowest) to 8 (highest) with higher scores indicating higher levels of coping ability.

Full Information

First Posted
August 31, 2021
Last Updated
February 8, 2022
Sponsor
The Zucker Hillside Hospital
Collaborators
College of Staten Island, the City University of New York
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1. Study Identification

Unique Protocol Identification Number
NCT05047081
Brief Title
From Intention to Action:Scoring Your College Goals
Official Title
Scoring Your College Goals: A Study to Increase Self-Efficacy in First-Year College Students
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 27, 2021 (Actual)
Primary Completion Date
March 1, 2022 (Anticipated)
Study Completion Date
April 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Zucker Hillside Hospital
Collaborators
College of Staten Island, the City University of New York

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The current study aims to prevent the developmental of mental health symptoms in first-year college students through providing a workshop aimed at preparing students for the academic, social, and personal challenges associated with typical college experiences. Specifically, the study hypothesizes that first-year student students who participate in a workshop on college readiness will report fewer symptoms of depression and anxiety, higher levels of self-esteem, and better academic performance compared to a similar group of students who do not receive the intervention (the control group). Students in the intervention group will participate in a one-time, two-hour workshop that discusses expectations about college, setting goals that are aligned with one's values, predicting barriers to achieving these goals, and how to overcome these obstacles. The workshop will provide students with external resources (both on and off campus) for obtaining additional support to address barriers that arise during their college experiences. Students will complete questionnaires about symptoms of depression, anxiety, and their ability to cope with stress before the workshop, after the workshop, and at the end of their first semester. At the end of the Fall 2021 semester, students will be asked to share information about their Grade Point Average (GPA) and academic status. The investigators predict that at the end of the semester, those students who participated in the workshop will report lower levels of depression, anxiety and stress, higher levels of self-esteem, and a higher GPA compared to students who did not receive the intervention. Students who participated in the workshop will also be more likely to continue (enrolled in the Spring 2022 semester) compared to controls.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Anxiety
Keywords
Depression, Anxiety, College Mental Health, Mental Health Prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
126 (Actual)

8. Arms, Groups, and Interventions

Arm Title
College Workshop Arm
Arm Type
Experimental
Arm Description
Intervention
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Behavioral
Intervention Name(s)
Scoring Your College Goals Workshop
Intervention Description
A two-hour virtual college readiness workshop.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo Treatment-As-Usual Group which does not receive the workshop intervention
Primary Outcome Measure Information:
Title
Change in Self-Reported Depression Symptoms on the DASS-21
Description
Change in Depression Symptoms as measured by self-report on the Depression sub scale of the Depression, Anxiety and Stress Scale (DASS-21). Each sub scale of the DASS-21 has a range of 0-(lowest) to 42 (highest) with higher scores indicating worsening levels of psychopathology.
Time Frame
Three Months
Title
Change in Anxiety Symptoms as measured by the DASS-21
Description
Participants in the intervention arm but not the placebo group will demonstrate change in Depression Symptoms as measured by participant self-report on the Anxiety subscale of the Depression, Anxiety and Stress Scale (DASS-21).
Time Frame
Three Months
Secondary Outcome Measure Information:
Title
Change in self-efficacy as measured by the Coping Self-Efficacy Scale
Description
Participants in the intervention group but not the control group will demonstrate significant change in self-reported self-efficacy scores as measured by the Coping Self-Efficacy Scale (CSE). Each sub scale of the CSE has a range of scores from 0 (lowest) to 60 (highest) with a higher score representing better (improved) coping self-efficacy.
Time Frame
Three Months
Title
Change in Coping abilities as measured by the Brief COPE
Description
Participants in the intervention group but not the control group will demonstrate significant change in their ability to cope with stress as measured by self-reported total scores on the Brief COPE. The fourteen sub scales of the Brief COPE each have a range of 0 (lowest) to 8 (highest) with higher scores indicating higher levels of coping ability.
Time Frame
Three Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: First-year, first semester freshman enrolled in Psychology 100 courses at CUNY College of Staten Island. Exclusion Criteria: Under 18 years old Violation of inclusion criteria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Timothy I Michaels, PhD
Organizational Affiliation
The Zucker Hillside Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
CUNY College of State Island
City
Staten Island
State/Province
New York
ZIP/Postal Code
10314
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

From Intention to Action:Scoring Your College Goals

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