Clinical Intervention Psychosis and Addiction

NCT ID: NCT01411566

Last Updated: 2011-08-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

EARLY_PHASE1

Total Enrollment

122 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-01-31

Study Completion Date

2011-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to evaluate an integrative therapeutic concept for schizophrenic patients with comorbid substance use disorder.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Psychosis Substance Abuse

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Treatment

Group Type EXPERIMENTAL

Skills trainig for patients with dual diagnosis

Intervention Type BEHAVIORAL

Skills trainig for patients with dual diagnosis

Control

Group Type ACTIVE_COMPARATOR

regular treatment

Intervention Type BEHAVIORAL

regular treatment

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Skills trainig for patients with dual diagnosis

Skills trainig for patients with dual diagnosis

Intervention Type BEHAVIORAL

regular treatment

regular treatment

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Schizophrenia
* Addiction
* Written statement of agreement
* Majority

Exclusion Criteria

* Acute psychosis
* Further neuropsychiatric disorder
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Cologne

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

University of Cologne

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Joerg Daumann, PhD

Role: STUDY_CHAIR

University of Cologne

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

LVR Clinic Cologne - Academic Clinic of the University of Cologne

Cologne, , Germany

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Germany

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Joerg Daumann, PhD

Role: primary

+49 221 478 ext. 87113

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Koeln-Fortune 104/2010

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Efficacy of ISST in Schizophrenia
NCT02678858 COMPLETED NA