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Psychodynamic Psychotherapy for Psychosis

Psychodynamic Psychotherapy for Psychosis: An Empirical Pilot Study of Efficacy, Therapeutic Action, and Machine Learning Analysis of Within-Session Speech and Behavior

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04415541
Enrollment
0
Registered
2020-06-04
Start date
2021-05-31
Completion date
2021-08-31
Last updated
2021-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psychotic Disorders

Brief summary

The broad goals of our pilot study are to (1) determine whether psychodynamic psychotherapy for psychosis (PPfP), relative to treatment as usual (TaU), can maintain or augment clinical and functional benefits for patients who have achieved initial recovery in our coordinated specialty care (CSC) early psychosis treatment program; (2) to conduct novel empirical study of how various psychodynamic factors may inform candidate selection, mediate therapeutic effects, and influence relational aspects of the therapy; and (3) to conduct a detailed study of how features of therapist and patient speech and behavior influence therapeutic outcomes, therapeutic alliance alliance, and relational process. This registration focuses on the first goal.

Interventions

Intensive psychotherapy that is psychodynamically oriented.

BEHAVIORALUsual Care

Conventional treatment offered in the community.

Sponsors

University of Southern California
CollaboratorOTHER
American Psychoanalytic Association
CollaboratorUNKNOWN
Yale University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* completed the 2-3 year Coordinated Specialty Care (CSC) program * judged by present provider to be in an intermediate or advanced phase of recovery * had first episode of psychosis within the 3 years prior to enrollment

Exclusion criteria

* established diagnosis of primary affective disorder, psychosis secondary to substance use or a medical illness * inability to communicate in English * eligibility for Department of Developmental Services * legally mandated to enter treatment.

Design outcomes

Primary

MeasureTime frameDescription
Overall Functioning - SocialFrom enrollment up to 5 years from enrollment.The Global Functioning: Social scale will be used, with symptoms rated 1 (most impaired) to 10 (superior functioning).
Overall Functioning - RoleFrom enrollment up to 5 years from enrollment.The Global Functioning: Role scale will be used, with symptoms rated 1 (most impaired) to 10 (superior functioning).
Overall Symptom SeverityFrom enrollment up to 5 years from enrollment.The Positive and Negative Symptom Scale (PANSS) will be used. This is a 30 item scale. Each item is measured on a 7-point scale from 1 (absent) to 7 (extreme). Items are summed to obtain an overall score.

Secondary

MeasureTime frameDescription
Symptom Severity (Positive Symptoms)From enrollment up to 5 years from enrollment.The positive symptoms subscale of the Positive and Negative Symptom Scale (PANSS) will be used. Each item is measured on a 7-point scale from 1 (absent) to 7 (extreme). Subscale items are summed to obtain a positive symptom score.
Symptom Severity (Negative Symptoms)From enrollment up to 5 years from enrollment.The negative symptoms subscale of the Positive and Negative Symptom Scale (PANSS) will be used. Each item is measured on a 7-point scale from 1 (absent) to 7 (extreme). Subscale items are summed to obtain an overall score.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026