CREATION Health Assessment Tool for College Students (CHAT-CS)

February 6, 2020 updated by: AdventHealth

Development and Psychometric Test of CREATION Health Assessment Tool for College Students

CREATION Health encompasses eight whole-person care principles: Choice, Rest, Environment, Activity, Trust, Interpersonal-Relationships, Outlook, and Nutrition. An existing initial tool consisting of 74 items related to the eight CREATION Health principles and college students' wellbeing were generated by subject/methodology experts. To develop the CREATION Health Assessment Tool for College Students (CHAT-CS), this initial tool needs to be finalized through item reductions and validations in the population of college students.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

CREATION Health encompasses eight whole-person care principles: Choice, Rest, Environment, Activity, Trust, Interpersonal-Relationships, Outlook, and Nutrition.

Based on these principles, a health and wellness program, CREATION Health Wellness Program was developed. Since then various education/training plans using mind-body-spirit approaches have been implemented for different populations. Recently the Adventist Health System has plan to assess Adventist university students' health wellbeing and develop strategies to intervene and thus improve their overall wellbeing. However, literature review found that measures of these eight CREATION Health principles are often discrete and inconsistent. Therefore, there is an urgent need for a comprehensive, consistent assessment tool.

An existing initial tool consisting of 74 items related to the eight CREATION Health principles and college students' wellbeing were generated by subject/methodology experts. To develop the CREATION Health Assessment Tool for College Students (CHAT-CS), this initial tool needs to be finalized through item reductions and validations in the population of college students.

Study Type

Observational

Enrollment (Actual)

474

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Alabama
      • Huntsville, Alabama, United States, 35896
        • Oakwood University
    • Michigan
      • Berrien Springs, Michigan, United States, 49104
        • Andrews University
    • Nebraska
      • Lincoln, Nebraska, United States, 68506
        • Union College
    • Ohio
      • Kettering, Ohio, United States, 45429
        • Kettering College
    • Tennessee
      • Collegedale, Tennessee, United States, 37315
        • Southern Adventist University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Adult undergraduate students in college/university

Description

Inclusion Criteria:

  • Undergraduate college student
  • Age 18 or more years
  • Must be able to read and understand ENglish

Exclusion Criteria:

  • Have previously taken the University Wellness Assessment

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Establish reliability using Cronbach's alpha
Time Frame: Through December, 2018
Cronbach's (alpha) is a coefficient of reliability. The theoretical l value of the Cronbach's alpha varies from 0 to 1. A higher score indicates higher reliability.
Through December, 2018

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Item deduction
Time Frame: Through May, 2019
  • If an item is highly correlated with another item (item redundancy), consider removing one of the two items (correlation >.70)
  • If an item is not correlated (<.30) with other items, then consider eliminating this item
  • If an individual item has a weak loading on all factors (.39 or less), consider removing
  • If an item has a high loading (.40 or more) on multiple factors, consider modification or elimination
Through May, 2019

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Johanson, G.A. and Brooks, G.P. (2010) Initial scare development sample size for pilot studies. Educational and Psychological Measurement, 70, 394-400.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

October 1, 2018

Primary Completion (ACTUAL)

July 9, 2019

Study Completion (ACTUAL)

July 9, 2019

Study Registration Dates

First Submitted

August 22, 2018

First Submitted That Met QC Criteria

August 23, 2018

First Posted (ACTUAL)

August 27, 2018

Study Record Updates

Last Update Posted (ACTUAL)

February 7, 2020

Last Update Submitted That Met QC Criteria

February 6, 2020

Last Verified

February 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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