- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06825000
Scientific Information and Beliefs About Psychological Therapy
April 12, 2026 updated by: Golnaz Tabibnia, University of California, Irvine
The Effects of Science Education on Beliefs and Wellness
The success of psychological therapy can be impacted by patients' beliefs, such as their belief in their own ability to complete therapy and their belief that therapy will work.
The goal of this clinical trial is to learn whether and when scientific information about distress and coping can affect beliefs about psychological therapy in adults who experience anxiety.
This study will compare two different types of scientific information in a one-hour study.
Participants will view educational videos for 30 minutes and complete surveys, including quiz questions about the videos and surveys about their beliefs about psychological therapy.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
262
Phase
- Not Applicable
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
-
-
California
-
Irvine, California, United States, 92697
- University of California
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Probable anxiety disorder based on the Overall Anxiety Severity and Impairment Scale (OASIS) score
- Fluent in English
- Willingness and ability to comply with the protocol
- Age 18-80
- The ability to enroll in the study through Prolific.com
Exclusion Criteria:
- Having previously seen the study's videos
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
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Neuro-Ed Group
neuroscience education
|
30 minutes of videos about the neuroscience of stress, fear, emotion-regulation, and therapy.
Other Names:
|
|
Active Comparator: Psycho-Ed Group
psychological science education
|
30 minutes of videos about the psychological science of stress, fear, emotion-regulation, and therapy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Treatment Self-Efficacy
Time Frame: Immediately before and immediately after watching the videos
|
Measured through self-report on selected items from a version of the validated Bergen Genetic Counseling Self-Efficacy Scale that was previously adapted for treatment self-efficacy in anxiety disorders.
The items are rated on a scale of 1-10, with higher numbers indicating greater self-efficacy.
|
Immediately before and immediately after watching the videos
|
|
Treatment Expectancy
Time Frame: Immediately before and immediately after watching the videos
|
Measured through self-report on a subscale of the validated Credibility/Expectancy Questionnaire, assessing participants' expectation of treatment efficacy.
Each item is rated on a scale of 1-9 or 0%-100%, with higher numbers indicating more optimistic expectancy.
|
Immediately before and immediately after watching the videos
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Treatment Acceptability
Time Frame: Immediately after watching the videos
|
Participants will rate on a scale of 1-7 how useful, interesting, credible, and easy-to-understand they found the information in the videos.
Greater numbers indicate greater acceptability.
|
Immediately after watching the videos
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Golnaz Tabibnia, PhD, University of California, Irvine
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)
May 21, 2025
Primary Completion (Actual)
October 9, 2025
Study Completion (Actual)
October 17, 2025
Study Registration Dates
First Submitted
January 23, 2025
First Submitted That Met QC Criteria
February 8, 2025
First Posted (Actual)
February 13, 2025
Study Record Updates
Last Update Posted (Actual)
April 14, 2026
Last Update Submitted That Met QC Criteria
April 12, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 3274
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
De-identified IPD that underlie results in a publication may be provided to qualified researchers with academic interest in science education and mental health.
Approval of the request and execution of all applicable agreements may be prerequisites to the sharing of data with the requesting party.
IPD Sharing Time Frame
Data requests can be submitted starting 9 months after article publication, and the data will be made accessible for up to 5 years after study completion.
IPD Sharing Access Criteria
Researchers requesting data will first be asked to provide a research proposal.
Pending approval of the proposal, they will then be asked to sign a data sharing agreement, which will include restrictions against attempting to identify study participants, on redistribution of the data to third parties, on use of the data for commercial purposes, as well as requirements to electronically secure the data while in use, to destroy the data after analyses are completed, for reporting responsibilities, and for proper acknowledgement of the data resource.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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