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Diagnosis, Dual (Psychiatry) clinical trials

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NCT ID: NCT05115266 Not yet recruiting - Clinical trials for Diagnosis, Dual (Psychiatry)

Efficacy of Animal-assisted Therapy in Patients With Borderline Personality Disorder and Addictions.

Start date: April 30, 2022
Phase: N/A
Study type: Interventional

Animal-assisted therapy (AAT) is a complementary intervention of therapy that has shown positive results in the treatment of various pathologies. This study assesses the viability of the implementation and the effectiveness of an AAT program in patients diagnosed with borderline personality disorder and substance abuse disorder. Our hypotheses are that participation in the TAA program will reduce negative symptoms, improve the quality of life of people with dual pathology, whose mental illness is schizophrenia, and increase adherence to treatment for people with dual pathology, whose mental disorder it's schizophrenia.

NCT ID: NCT05103865 Completed - Clinical trials for Diagnosis, Dual (Psychiatry)

Animal-Assisted Therapy in the Residential Treatment of Schizophrenia and Addictions

Start date: November 3, 2015
Phase: N/A
Study type: Interventional

Animal-assisted therapy (AAT) is a complementary intervention of therapy that has shown positive results in the treatment of various pathologies. This study assesses the viability of the implementation and the efectiveness of an AAT program in patients diagnosed with substance abuse disorder and associated mental disorders (dual pathology).

NCT ID: NCT04442776 Not yet recruiting - Clinical trials for Diagnosis, Dual (Psychiatry)

Dual Integrated Attention Program (DAIP) in People With Severe Dual Diagnosis

PAI-D
Start date: September 1, 2020
Phase: N/A
Study type: Interventional

Aim: validate a Dual Integrated Attention Program (D-AIP) for mental health nursing in people with Severe Dual Diagnosis admitted to a psychiatric hospitalization unit Design: Randomized Controlled Trial. Population: Inpatients with dual diagnosis.

NCT ID: NCT01135420 Active, not recruiting - Clinical trials for Diagnosis, Dual (Psychiatry)

Dual Diagnosis Inpatients: Telephone Monitoring RCT to Improve Outcomes

Start date: April 2011
Phase: Phase 2
Study type: Interventional

This research program will improve the care and treatment outcomes of dually diagnosed veterans who receive inpatient psychiatry care, and decrease their use of VA inpatient mental health services. It will increase the use of substance abuse outpatient care and 12-step groups to benefit recovery, reduce rehospitalizations, and reduce costs for VA.

NCT ID: NCT00583440 Completed - Alcoholism Clinical Trials

12-step Facilitation for the Dually Diagnosed

TSFDD
Start date: September 2005
Phase: Phase 1/Phase 2
Study type: Interventional

This is a randomized trial testing the efficacy of a modified 12-step facilitation therapy for individuals with serious mental illness and alcohol use disorders, compared to usual treatment. 135 participants are randomized in 2:1 ratio to the modified 12-step facilitation (12 sessions of individual counseling) vs. treatment as usual. The primary hypothesis is that those receiving 12-step facilitation will have better drinking outcomes (percent days abstinence and drinks per drinking day)at end of treatment.

NCT ID: NCT00237822 Completed - Drug Use Disorders Clinical Trials

Increasing Treatment Adherence in Co-Occurring Psychiatric and Drug Use Disorders

Start date: September 2003
Phase: Phase 2
Study type: Interventional

The investigators are proposing a study of treatment adherence in co-occurring psychiatric and drug use disorders (COD). The proposed study uses a 3-cell/condition design, within which 75 adult outpatients with co-occurring psychiatric disorders and drug abuse/dependence (CODDA) will be randomly assigned to one of the following brief, 8-week, manual-guided interventions following a 2-week "Assessment Only" baseline period: 1. Adherence Feedback (AF); this condition will entail weekly, 20-25 minute sessions of AF, which is a procedure that represents a technological advancement developed by Cramer et al. (1989, 1995, and 1999) and is based on the use of adherence data from the microelectronic monitor in Medication Event Monitoring System (MEMS) caps, 2. AF + Contingency Management (AF + CM); in this condition, participants will receive AF, as described above, PLUS contingency management. CM is based on the behavioral learning theory, which suggests that the occurrence of a behavior is increased as a function of the rate at which it is positively reinforced or rewarded, or 3. AF + Motivational Enhancement Therapy (AF + MET); in this condition, patients will receive AF, as described above, PLUS motivational enhancement therapy. MET is based on the idea that an effective way to motivate behavior change is to assist patients in clarifying their ambivalence (i.e., reasons for and against changing/adhering), utilizing a series of strategies based on client-centered psychotherapy, self-efficacy theory, and social psychology. The study will allow the evaluation of three hypotheses: 1. AF + MET is superior to AF + CM, 2. AF + MET is superior to AF alone, and 3. AF + CM is superior to AF alone. Primary outcome measures are: 1. rates of adherence to medication (i.e., selective serotonin reuptake inhibitors or SSRIs), as measured by MEMS caps and self-report, 2. rates of counseling attendance, and 3. reductions in illicit drug use, including achievement of abstinence, as assessed by twice-weekly urine toxicology tests and self-report. Secondary outcomes include reductions in psychiatric symptomatology and rates of re-hospitalization. The investigators will also evaluate the relationship between adherence and primary and secondary outcomes.