- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03053765
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
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
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Iowa
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Iowa City, Iowa, United States, 52242
- University of Iowa
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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.
Sponsor
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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