Effective Implementation of Interpersonal Psychotherapy
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT03170908 |
Recruitment Status :
Not yet recruiting
First Posted : May 31, 2017
Last Update Posted : April 8, 2019
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Condition or disease | Intervention/treatment |
---|---|
Depressive Symptoms | Behavioral: Interpersonal Psychotherapy |
Study Type : | Observational |
Estimated Enrollment : | 425 participants |
Observational Model: | Ecologic or Community |
Time Perspective: | Prospective |
Official Title: | Pragmatic Strategies for Assessing and Enhancing High Fidelity Delivery of Interpersonal Psychotherapy (IPT) in Community Practice |
Estimated Study Start Date : | July 2019 |
Estimated Primary Completion Date : | June 2021 |
Estimated Study Completion Date : | June 2021 |

Group/Cohort | Intervention/treatment |
---|---|
Phase I Patients
Patients with depression receiving community-based services will receive Interpersonal Psychotherapy
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Behavioral: Interpersonal Psychotherapy
Interpersonal Psychotherapy (IPT) is an empirically-validated time-limited treatment for depression |
Phase II Patients
Patients with depression receiving community-based services will receive Interpersonal Psychotherapy
|
Behavioral: Interpersonal Psychotherapy
Interpersonal Psychotherapy (IPT) is an empirically-validated time-limited treatment for depression |
- PHQ-9 [ Time Frame: one year ]Patient Health Questionnaire-9

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Ages Eligible for Study: | 18 Years to 99 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- age 18-99
- diagnosis of depressive disorder
- being treated with IPT in community settings
Exclusion Criteria:
- none

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03170908
United States, Iowa | |
University of Iowa | |
Iowa City, Iowa, United States, 52242 |
Responsible Party: | Scott P. Stuart, Professor, Dept of Psychiatry, University of Iowa |
ClinicalTrials.gov Identifier: | NCT03170908 |
Other Study ID Numbers: |
201705766 1R01MH112624 ( U.S. NIH Grant/Contract ) |
First Posted: | May 31, 2017 Key Record Dates |
Last Update Posted: | April 8, 2019 |
Last Verified: | April 2019 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Plan Description: | we do not plan to share IPD |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Depression Behavioral Symptoms |