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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04759313
Other study ID # imagenarrative
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 15, 2021
Est. completion date February 28, 2022

Study information

Verified date February 2023
Source University of Utah
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The PI developed the Image Narrative Intervention (INI) based on the research using visual images in which visual images and narratives were found to support trauma survivors in narrating their experiences and in meaning making. The proposed study is the first study to test the therapeutic effect of the INI program. The investigators propose to assess, both qualitatively and quantitatively, the feasibility and preliminary effect of the INI through a pilot randomized control trial (RCT) design with a wait list control.


Description:

AIM 1. To understand the unique experiences of emerging adult college students during the Covid-19 pandemic (especially around the themes of the self, relationships with others, and the future). AIM 2. To evaluate the feasibility of the INI for emerging adult college students during the Covid-19 pandemic, both quantitatively and qualitatively. AIM 3. To evaluate the preliminary efficacy of the INI on distress, PTG, Quality of Life and Meaning-Making.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date February 28, 2022
Est. primary completion date February 28, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 29 Years
Eligibility Inclusion Criteria: - 18-29 in age - college students at the University of Utah - reporting moderate or higher levels of distress in DASS21 Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Image Narrative
Each participant will take part in a 5-week program of weekly 1-hour telehealth sessions with the PI or a social work PhD student facilitator trained in the INI by the PI.

Locations

Country Name City State
United States University of Utah Salt Lake City Utah

Sponsors (1)

Lead Sponsor Collaborator
University of Utah

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary DASS (Depression, Anxiety and Stress Scale) 21 measuring distress, 0-63, higher is worse change through study completion, an average of 3 months
Primary PTGI (posttraumatic growth index) measuring posttraumatic growth, 0-105, higher is better change through study completion, an average of 3 months
Primary WHOQOL (WHO quality of life)-bref measuring quality of life, 0-100, higher is better change through study completion, an average of 3 months
Primary MLQ (meaning in life) measuring meaning making, 0-70, higher is better change through study completion, an average of 3 months
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