Optimizing Fidelity of Interpersonal Psychotherapy

June 6, 2022 updated by: University of Iowa

Optimizing Fidelity of Interpersonal Psychotherapy for Depression

The study is designed to develop and validate an instrument to measure quality and adherence to IPT for research and training purposes. The measure is now being used to evaluate training in IPT.

Study Overview

Status

Terminated

Conditions

Intervention / Treatment

Detailed Description

The study is a randomized trial comparing 4 different methods of follow-up training in IPT. Following initial 2-day training, participant therapists will be randomized to either individual supervision, group supervision, an internet-based training program, or autodidactic training. Participants will be followed for a year to determine their use of IPT, outcomes with patients, and adherence and quality of IPT in 4 case portfolios. The adherence measure for IPT developed in Phase I of the project is being used as the gold standard measure of IPT fidelity.

Study Type

Interventional

Enrollment (Actual)

115

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

    • Iowa
      • Iowa City, Iowa, United States, 52242
        • University of Iowa

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

21 years to 99 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Active and licensed therapist conducting psychotherapy treatment; naïve to training in IPT

Exclusion Criteria:

  • Inactive or not treating patients

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Individual Supervision in IPT
Bi-weekly individual case supervision in IPT
Follow-up training in IPT to determine which best enhances fidelity
Experimental: Group Supervision in IPT
Bi-weekly group supervision in IPT in groups of 4-6 therapists
Follow-up training in IPT to determine which best enhances fidelity
Experimental: Internet-Based Training in IPT
Access to internet-based training in IPT to review information learned in initial 2-day training
Follow-up training in IPT to determine which best enhances fidelity
No Intervention: Autodidactic Training in IPT
Clinicians allowed access to training materials and can engage in self-study

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
expert evaluation of conduct of IPT using IPT Quality and Adherence Measure
Time Frame: one year
The "IPT Quality and Adherence Measure" is the title of a single outcome measure used to assess clinicians performance of IPT
one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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)

August 3, 2012

Primary Completion (Actual)

January 31, 2020

Study Completion (Actual)

January 31, 2020

Study Registration Dates

First Submitted

August 9, 2016

First Submitted That Met QC Criteria

February 10, 2017

First Posted (Actual)

February 15, 2017

Study Record Updates

Last Update Posted (Actual)

June 9, 2022

Last Update Submitted That Met QC Criteria

June 6, 2022

Last Verified

June 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • R33MH097041 (U.S. NIH Grant/Contract)

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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