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Completed Not applicable Interventional Accepts healthy volunteers

Activating Messages for Enhancing Primary Care Practice (AMEP2): Effectiveness Study

ClinicalTrials.gov ID: NCT01144104

Public ClinicalTrials.gov record NCT01144104. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 4:04 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Targeted and Tailored Messages to Enhance Depression Care

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial consists of two linked substudies. Substudy 1: Activating Messages for Enhancing Primary Care Practice (AMEP2): Effectiveness Study Substudy 2: Activating Messages for Enhancing Primary Care Practice (AMEP2): Toxicity Study The purpose of the Effectiveness Study is to assess the comparative effectiveness of three multimedia educational interventions (a targeted educational video, a tailored interactive multimedia computer program, and an "attention control") for increasing the likelihood that primary care patients with significant depressive symptoms will seek appropriate care (n = 510). The primary study outcomes are provision of minimally acceptable initial care, reductions in depression-related stigma, and improvement in depression symptoms. (See Process of Care and Patient Outcomes in Primary Outcome Measure section.) The purpose of the Toxicity Study is to assess the potential benefits (reduced stigma) and harms (inappropriate prescribing) associated with three multimedia depression educational interventions when administered to patients with few or no depressive symptoms (n = 308). The primary outcomes relating to this outcome are reducing depression-related stigma and reducing unnecessary prescribing. (See Toxicity in Primary Outcome Measure section.) Both studies will look at the secondary outcome measure of patient requests for depression treatment.

Study identification

NCT ID
NCT01144104
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
925 participants

Conditions and interventions

Eligibility (public fields only)

Age range
25 Years to 70 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2010
Primary completion
Oct 31, 2011
Completion
May 31, 2014
Last update posted
May 29, 2017

2010 – 2014

United States locations

U.S. sites
6
U.S. states
1
U.S. cities
4
Facility City State ZIP Site status
Sutter Health - Elk Grove Family Medicine Elk Grove California 95758
VA Northern California Healthcare System Mather California 95655
Kaiser Permanente - Point West Sacramento California 95815
University of California, Davis Sacramento California 95817
San Francisco VA Medical Center San Francisco California 94121
University of California, San Francisco San Francisco California 94143

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01144104, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 29, 2017 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01144104 live on ClinicalTrials.gov.

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