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NCT03170908 Clinical Trial

Effective Implementation of Interpersonal Psychotherapy

Depressive Symptoms Clinical Trial

Official title:
Pragmatic Strategies for Assessing and Enhancing High Fidelity Delivery of Interpersonal Psychotherapy (IPT) in Community Practice

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT03170908
Other study ID # 201705766
Secondary ID 1R01MH112624
Status Terminated
Phase
First received
Last updated
Start date May 19, 2017
Est. completion date December 6, 2019

Study information
Verified date June 2022
Source University of Iowa
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study is designed to observe the impact of improved measures of the fidelity on the community delivery of Interpersonal Psychotherapy. Pairs of therapist-patient dyads will be observed, first to develop and test brief measures of fidelity, and then to correlate those measures with symptomatic outcomes.

Description:

The study is designed to observe the impact of improved measures of the fidelity on the community delivery of Interpersonal Psychotherapy. In Phase I, 250 pairs of therapist-patient dyads will be observed as IPT Fidelity measures are developed and validated. In Phase II, 175 pairs of therapist-patient dyads will be observed to prospectively validate the IPT Fidelity measures with longitudinal outcomes on the PHQ-9.

Recruitment information / eligibility
Status Terminated
Enrollment 13
Est. completion date December 6, 2019
Est. primary completion date December 6, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - age 18-99 - diagnosis of depressive disorder - being treated with IPT in community settings Exclusion Criteria: - none

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Interpersonal Psychotherapy
Interpersonal Psychotherapy (IPT) is an empirically-validated time-limited treatment for depression

Locations
Country Name City State
United States University of Iowa Iowa City Iowa

Sponsors (2)
Lead Sponsor Collaborator
University of Iowa National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary PHQ-9 Patient Health Questionnaire-9 one year
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