Feasibility of a Novel Process-based Treatment for Patients With Psychosis

NCT04874974 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 37

Last updated 2023-10-23

No results posted yet for this study

Summary

The purpose of this single-arm feasibility study is to develop and pilot test a novel process-based and modular group therapy approach for patients with acute psychotic symptoms in an inpatient setting.

Conditions

  • Schizophrenia
  • Schizotypal Disorder
  • Delusional Disorder
  • Brief Psychotic Disorder
  • Shared Psychotic Disorder
  • Schizoaffective Disorder
  • Other Psychotic Disorder Not Due to A Substance or Known Physiological Condition
  • Unspecified Psychosis Not Due to a Substance or Known Physiological Condition
  • Manic Episode, Severe With Psychotic Symptoms
  • Bipolar Disorder, Current Episode Manic Severe With Psychotic Features
  • Bipolar Disorder, Current Episode Depressed, Severe, With Psychotic Features
  • Major Depressive Disorder, Single Episode, Severe With Psychotic Features
  • Major Depressive Disorder, Recurrent, Severe With Psychotic Symptoms

Interventions

BEHAVIORAL

Metacognitive and Defusion Training

Module I will give a brief introduction into the rational of the therapy and explain the terms cognitive biases and relational responding and their role in the development of psychological problems (psychosis) in a simple language and with the help of examples and small exercises. The principle of metacognition and cognitive defusion in psychotherapy will be made clear. An outlook on the procedures and the goals of the group therapy will be given. Module II will include interventions adapted from the MCT manual (Moritz et al., 2017) and Module III with consist of defusion strategies taken from the ACT group manual (Dambacher et al., 2020) and existing studies on ACT and psychosis (Bach et al., 2013; Gaudiano \& Herbert, 2006).

Sponsors & Collaborators

  • Max-Planck-Institute of Psychiatry

    lead OTHER

Principal Investigators

  • Susanne Lucae, MD, Prof. · Max-Planck-Institute of Psychiatry

  • Johannes M Kopf-Beck, PhD · Max-Planck-Institute of Psychiatry

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-10
Primary Completion
2022-03-10
Completion
2023-09-23

Countries

  • Germany

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04874974 on ClinicalTrials.gov