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Responses to Information on Treatments for Depression

Not Applicable
Completed
Conditions
Depressive Symptoms
Interventions
Other: CBT with Personalization
Other: ADM without Personalization
Other: CBT without Personalization
Other: Combined Treatment with Personalization
Other: Combined Treatment without Personalization
Other: ADM with Personalization
Registration Number
NCT04639765
Lead Sponsor
Ohio State University
Brief Summary

The purpose of this study is to determine the impact of different messages about depression treatments.

Detailed Description

Participants recruited through Amazon Mechanical Turk (MTurk) will complete a screening questionnaire and provided the opportunity to consent to participate. Upon entry to the study, eligible participants will complete several questionnaires pre- and post-randomization. Randomization will be to view either a video detailing a type of depression treatment (cognitive behavioral therapy, antidepressant medication, or the combination of both treatments) with and without an emphasis on personalization. A no video condition is also included.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
300
Inclusion Criteria
  • PHQ-9 Score indicating a history of elevated depression symptoms
  • A high MTurk completion rate
  • Must pass all attention checks inserted into the questionnaires
  • No history of treatment for depression
Exclusion Criteria
  • none

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
CBT with PersonalizationCBT with PersonalizationVideo provides information about cognitive behavioral therapy and describes how treatment can be personalized.
ADM without PersonalizationADM without PersonalizationVideo provides information about antidepressant medications.
CBT without PersonalizationCBT without PersonalizationVideo provides information about cognitive behavioral therapy.
Combined Treatment with PersonalizationCombined Treatment with PersonalizationVideo provides information on the combined treatment of cognitive behavioral therapy with antidepressant medications and describes how treatment can be personalized.
Combined Treatment without PersonalizationCombined Treatment without PersonalizationVideo provides information on the combined treatment of cognitive behavioral therapy with antidepressant medications.
ADM with PersonalizationADM with PersonalizationVideo provides information about antidepressant medications and describes how treatment can be personalized.
Primary Outcome Measures
NameTimeMethod
Regressed change from baseline in expectations on the Credibility/Expectancy Questionnaire (CEQ)Up to 90 minutes to complete assessment. Assessed immediately pre- and post-intervention (on the same day)

The CEQ is a validated, commonly used measure assessing views of the credibility and expectations for benefit from a treatment.

Regressed change from baseline in prognostic pessimism on an adapted version of the Perceptions of Depression Scale (PDS)Up to 90 minutes to complete assessment. Assessed immediately pre- and post-intervention (on the same day)

Measured using an adapted version of the PDS, a validated scale measuring general prognostic pessimism. Minor changes to wording were made to directly address the three different interventions in the study (CBT, ADM, Combined Treatment).

Secondary Outcome Measures
NameTimeMethod
Regressed Change from baseline on the Beck Hopelessness Scale (BHS)Up to 90 minutes to complete assessment. Assessed immediately pre- and post-intervention (on the same day)

The BHS is the most widely used measure for hopelessness, and has been shown to be valid and reliable.

Regressed change from baseline in affect on the Positive and Negative Affectivity Scale (PANAS)Up to 90 minutes to complete assessment. Assessed immediately pre- and post-intervention (on the same day)

The PANAS is a widely used measure for positive and negative affect, and has been shown to be valid and reliable.

Regressed change from baseline in personal and perceived depression stigma on the Depression Stigma Scale (DSS).Up to 90 minutes to complete assessment. Assessed immediately pre- and post-intervention (on the same day)

The DSS is a valid and reliable measure for assessing personal and perceived stigma related to depression. The scale contains two subscales: personal stigma and perceived stigma.

Regressed change from baseline in beliefs on the etiology of depression on the Reasons for Depression Questionnaire (RFD).Up to 90 minutes to complete assessment. Assessed immediately pre- and post-intervention (on the same day)

The RFD is a valid and reliable measure for assessing one's beliefs on the etiology of depression.

Willingness to take a next step.Up to 90 minutes to complete assessment. Assessed at the end of the study questionnaires (same day)

Participants are given the option to learn more about finding cognitive behavioral therapy, antidepressant medications, or combination therapy. Based on their responses, they are provided links to relevant websites. This approach has been adopted from traditional marketing research to assess participants' responsiveness to a message.

Trial Locations

Locations (1)

Psychology Building 1835 Neil Avenue

🇺🇸

Columbus, Ohio, United States

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